Antibody Information
General Information of This Antibody
| Antibody ID | ANI0DEWGN |
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| Antibody Name | Vandortuzumab |
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| Organization | Genentech, Inc. |
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| Indication | Prostate cancer |
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| Synonyms |
DSTP3086S; MSTP2109A; RG7450;
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| Antibody Type | Monoclonal antibody (mAb) |
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| Antibody Subtype | Humanized IgG1-kappa |
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| Antigen Name | Metalloreductase STEAP1 (STEAP1) |
Antigen Info | ||||
| ChEMBI ID | ||||||
| Click to Show/Hide the Sequence Information of This Antibody | ||||||
| Heavy Chain Sequence |
EVQLVESGGGLVQPGGSLRLSCAVSGYSITSDYAWNWVRQAPGKGLEWVGYISNSGSTSY
NPSLKSRFTISRDTSKNTLYLQMNSLRAEDTAVYYCARERNYDYDDYYYAMDYWGQGTLV TVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPE LLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPRE EQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPP SREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVD KSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK Click to Show/Hide
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| Light Chain Sequence |
DIQMTQSPSSLSASVGDRVTITCKSSQSLLYRSNQKNYLAWYQQKPGKAPKLLIYWASTR
ESGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQYYNYPRTFGQGTKVEIKRTVAAPS VFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYS LSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Click to Show/Hide
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Each Antibody-drug Conjugate Related to This Antibody
Full Information of The Activity Data of The ADC(s) Related to This Antibody
Vandortuzumab vedotin [Phase 1 (discontinued)]
Identified from the Human Clinical Data
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Partial Response (PR) |
4%
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| Patients Enrolled |
Metastatic castration-resistant prostate cancer (CRPC).
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| Administration Dosage |
3 + 3 dose escalation study, 0.30 to 2.80 mg/kg intravenously given once every 3 weeks followed by cohort expansion at the recommended phase II dose or weekly (0.80 to 1.00 mg/kg).
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| Related Clinical Trial | |||||
| NCT Number | NCT01283373 | Clinical Status | Phase 1 | ||
| Clinical Description |
A phase 1, open-label study of the safety and pharmacokinetics of escalating doses of DSTP3086S in patients with metastatic castration-resistant prostate cancer.
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| Primary Endpoint |
DsTP3086S has acceptable safety at the recommended phase II dose level of 2.40 mg/kg once every 3 weeks.
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| Experiment 2 Reporting the Activity Date of This ADC | [2] | ||||
| Related Clinical Trial | |||||
| NCT Number | NCT01283373 | Clinical Status | Phase 1 | ||
| Clinical Description |
A phase 1, open-label study of the safety and pharmacokinetics of escalating doses of DSTP3086S in patients with metastatic castration-resistant prostate cancer.
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| Experiment 3 Reporting the Activity Date of This ADC | [3] | ||||
| Patients Enrolled |
Eligible patients require metastatic castration-resistant prostate cancer (≤2 prior chemo regimens for expansion cohort), ECOG 0-2, and measurable disease. Key exclusions include recent anticancer therapy (4-week washout), active infections, uncontrolled CNS metastases (>8 weeks post-radiotherapy if treated), corticosteroids >10mg/day prednisone, or prior mAb hypersensitivity.
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| Administration Dosage |
This study evaluated safety and activity of DSTP3086S (0.3-2.8 mg/kg IV) given every 3 weeks (q3w) to pts with CRPC.
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| Related Clinical Trial | |||||
| NCT Number | NCT01283373 | Clinical Status | PHASE1 | ||
| Clinical Description |
A Phase I, Open-Label Study of the Safety and Pharmacokinetics of Escalating Doses of DSTP3086S in Patients With Metastatic Castration-Resistant Prostate Cancer
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| Primary Endpoint |
Safety will be assessed through DLT monitoring during the first 21-day cycle to determine treatment tolerability.
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| Other Endpoint |
Comprehensive PK analyses including AUC, Cmax/Cmin, clearance, half-life, and volume of distribution will be conducted over a 1-year period to characterize drug exposure and metabolism.
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wO2024239281A1 c144 8.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.011 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.012 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
4.28 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C144 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.011 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.012 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
4.28 nM
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Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c482 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.013 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.014 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.35 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c200 7.8 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.014 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.02 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.98 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C200 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.014 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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|
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| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.02 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.98 nM
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Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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|
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c158 7.8 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.019 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.025 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
6.12 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C158 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.019 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
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| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.025 nM
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High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
6.12 nM
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Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c429 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.032 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.049 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.85 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c484 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.036 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.052 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.86 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c418 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.038 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.045 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.65 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c441 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.038 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.052 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
7.95 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c480 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.038 nM
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.046 nM
|
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.35 nM
|
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| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c112 4.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.039 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.047 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.28 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C112 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.039 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.047 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.28 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c218 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.045 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.065 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.85 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c431 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.045 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.059 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
7.86 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C218 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.045 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.065 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.85 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c237 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.048 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.065 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.23 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C237 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.048 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.065 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
5.23 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c289c [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.049 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.058 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
6.88 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C031 4.3 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.052 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.064 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.72 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C031 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.052 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1 and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.064 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.72 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c039 4.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.053 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.062 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.95 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C039 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.053 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.062 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.95 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c078 7.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.055 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.085 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
12.9 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C078 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.055 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.085 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
12.9 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c289 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.058 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.065 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
7.9 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c084c 4.1 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.075 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.093 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
11.7 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c225 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.075 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.082 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.8 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C084C [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.075 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.093 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
11.7 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C225 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.075 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.082 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.8 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c084 4.1 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.078 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.095 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c193 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.078 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.098 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
7.35 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C084 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.078 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.095 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C193 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.078 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.098 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
7.35 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c117 4.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.08 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.095 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
11.9 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c207c 4.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.08 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.087 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.45 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C117 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.08 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.095 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
11.9 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C207C [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.08 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.087 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
9.45 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c207 4.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.085 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.11 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.9 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C207 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.085 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.11 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.9 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c213 7.4 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.13 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.16 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
69.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C213 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.13 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.16 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
69.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c054 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.135 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.821 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
255.6 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C054 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.135 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.821 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
255.6 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c230 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.18 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.25 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
42.3 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C230 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.18 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.25 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
42.3 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c422 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.19 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.35 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
10.6 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c443 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.37 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.48 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
22.75 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c257 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.39 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.47 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
24.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C257 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.39 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.47 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
24.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c266c 4.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.56 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.72 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
27.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C266C [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.56 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.72 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
27.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c427 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.6 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.69 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
22.8 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c266 4.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.68 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.75 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
28.9 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C266 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.68 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.75 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
28.9 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c263 7.6 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.81 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.85 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
68.3 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C263 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.81 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.85 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
68.3 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c420 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.85 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.95 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
22.3 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c269c 4.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.89 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
1.07 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
51.8 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C269C [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.89 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
1.07 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
51.8 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c269 4.2 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.95 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
1.25 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
52.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
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| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c433 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.95 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
1.08 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
16.2 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C269 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
0.95 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
1.25 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
52.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 c060 7.7 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.15 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of C4-2B, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
12.08 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of PC3-4H7, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | PC3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
336.5 nM
|
|||
| Method Description |
MTT assays of the Steap1-ADCs against tumor cells of 22RV1, at 6000 cells, 96 h incubation
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
wO2024239281A1 C060 [Investigative]
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
8.15 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
C4-2B is both Steap1 and PSMA antigen high express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | C4-2B cells | CVCL_4784 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
12.08 nM
|
High Steap1 and PSMA expression (Steapl and PSMA +++) | ||
| Method Description |
PC-3-4H7 cell is both Steap1and PSMA antigen high express cells. To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | PC-3-4H7 cells | Homo sapiens | ||
| Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) |
336.5 nM
|
Low Steap1 and PSMA expression (Steap1 and PSMA+) | ||
| Method Description |
22RV1 is both Steapl and PSMA antigen low express cells.To run the assay,the cells (180 ul,6000cells)were added to each well in a 96-well plate and incubated for 24 hours at 37°C with 5%CO 2. Next,the cells were treated with test compounds (20ul)at various concentrations in appropriate cell culture medium (total volume,0.2 mL).The control wells contain cells and the medium but lack the test compounds.The plates were incubated for 120 hours at 37°C with 5%CO 2.MTT (5 mg/mL)was then added to the wells (20ul)and the plates were incubated for 1.5 hr at 37°C.The medium was carefully removed and DMSO (180ul)was added afterward.After it was shaken for 15min, the absorbance was measured at 490 nm and 570 nm with a reference filter of 620 nm.The inhibition% was calculated according to the following equation:inhibition%=[1- (assay-blank)/ (control-blank)]× 100.
Click to Show/Hide
|
||||
| In Vitro Model | Prostate carcinoma | 22RV1 cells | CVCL_1045 | ||
References
