General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0QRXDE
ADC Name
Trastuzumab-Gal-beta-1,4GlcNAc-MMAE
Synonyms
Trastuzumab Gal-beta-1;4GlcNAc MMAE
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Drug Status
Investigative
Indication
In total 1 Indication(s)
Breast cancer [ICD11:2C60-2C65]
Investigative
Drug-to-Antibody Ratio
2
Antibody Name
Trastuzumab
 Antibody Info 
Antigen Name
Receptor tyrosine-protein kinase erbB-2 (ERBB2)
 Antigen Info 
Payload Name
Monomethyl auristatin E
 Payload Info 
Therapeutic Target
Microtubule (MT)
 Target Info 
Linker Name
Gal-beta-1,4-GlcNAc
 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.
General Information of The Activity Data Related to This ADC
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Standard Type Value Units Cell Line Disease Model
Half Maximal Effective Concentration (EC50) 
> 10
uM
T-47D cells
Invasive breast carcinoma
Half Maximal Effective Concentration (EC50) 
0.04
6.08
nM
ng/mL
BT-474 cells
Invasive breast carcinoma
Half Maximal Effective Concentration (EC50) 
0.07
11.07
nM
ng/mL
SK-BR-3 cells
Breast adenocarcinoma
Full List of Activity Data of This Antibody-drug Conjugate
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 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.
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.
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.
In Vitro Model Breast adenocarcinoma SK-BR-3 cells CVCL_0033
References
Ref 1 Synthesis and Evaluation of Three Azide-Modified Disaccharide Oxazolines as Enzyme Substrates for Single-Step Fc Glycan-Mediated Antibody-Drug Conjugation. Bioconjug Chem. 2022 Jun 15;33(6):1179-1191.

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