General Information of This Payload
Payload ID
PAY0QJWYS
Name
Exatecan-L-Ala amide
Synonyms
compound 71
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Target DNA topoisomerase I (TOP1)
Structure
Formula
C25H25FN4O5
Isosmiles
CCC(C1=CC(NC([C@@H](N)C)=O)=C(F)C=C1N=C23)=C2CN4C3=CC([C@@]5(O)CC)=C(COC5=O)C4=O
InChI
InChI=1S/C25H25FN4O5/c1-4-12-13-6-19(29-22(31)11(3)27)17(26)8-18(13)28-21-14(12)9-30-20(21)7-16-15(23(30)32)10-35-24(33)25(16,34)5-2/h6-8,11,34H,4-5,9-10,27H2,1-3H3,(H,29,31)/t11-,25-/m0/s1
InChIKey
XSSRJRWJGBJKDA-FTJNGKRUSA-N
Pharmaceutical Properties
Molecule Weight
480.496
Polar area
136.54
Complexity
1452.107326
xlogp Value
2.0668
Heavy Count
35
Rot Bonds
4
Hbond acc
8
Hbond Donor
3
Each Antibody-drug Conjugate Related to This Payload
Full Information of The Activity Data of The ADC(s) Related to This Payload
wO2024239281A1 C078 [Investigative]
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
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.

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In Vitro Model Prostate carcinoma C4-2B cells CVCL_4784
Experiment 2 Reporting the Activity Date of This ADC [1]
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.

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In Vitro Model Prostate carcinoma PC-3-4H7 cells Homo sapiens
Experiment 3 Reporting the Activity Date of This ADC [1]
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.

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In Vitro Model Prostate carcinoma 22RV1 cells CVCL_1045
References
Ref 1 Targeted treatment of prostate cancers and other tumors by an antibody-drug conjugate