Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
| ADC ID |
DRG0QRXDE
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| ADC Name |
Trastuzumab-Gal-beta-1,4GlcNAc-MMAE
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| Synonyms |
Trastuzumab Gal-beta-1;4GlcNAc MMAE
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| Drug Status |
Investigative
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| Indication |
In total 1 Indication(s)
Investigative
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| Drug-to-Antibody Ratio |
2
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| Antibody Name |
Trastuzumab
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Antibody Info | ||||
| Antigen Name |
Receptor tyrosine-protein kinase erbB-2 (ERBB2)
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Antigen Info | ||||
| Payload Name |
Monomethyl auristatin E
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Payload Info | ||||
| Therapeutic Target |
Microtubule (MT)
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Target Info | ||||
| Linker Name |
Gal-beta-1,4-GlcNAc
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Linker Info | ||||
| Conjugate Type |
Endo-S2 performs a simultaneous deglycosylation and glycosylation of an antibody (Asn 279) with the drug-loaded disaccharide oxazoline substrates to give homogeneous ADCs.
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General Information of The Activity Data Related to This ADC
Revealed Based on the Cell Line Data
Full List of Activity Data of This Antibody-drug Conjugate
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal Effective Concentration (EC50) | > 10.00 uM | Negative HER2 expression (HER2-) | ||
| Method Description |
The cytotoxicity of the synthetic ADCs were tested in breast cancer cell lines SK-BR-3 and BT474 that have high levels of HER2 expression, and T47D that has low level expression of HER2 antigen.
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| In Vitro Model | Invasive breast carcinoma | T-47D cells | CVCL_0553 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal Effective Concentration (EC50) | 0.04 nM, 6.08 ng/mL | High HER2 expression (HER2+++) | ||
| Method Description |
The cytotoxicity of the synthetic ADCs were tested in breast cancer cell lines SK-BR-3 and BT474 that have high levels of HER2 expression, and T47D that has low level expression of HER2 antigen.
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| In Vitro Model | Invasive breast carcinoma | BT-474 cells | CVCL_0179 | ||
| Experiment 3 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal Effective Concentration (EC50) | 0.07 nM, 11.07 ng/mL | High HER2 expression (HER2+++) | ||
| Method Description |
The cytotoxicity of the synthetic ADCs were tested in breast cancer cell lines SK-BR-3 and BT474 that have high levels of HER2 expression, and T47D that has low level expression of HER2 antigen.
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| In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
References
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