Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
| ADC ID |
DRG0RIOUS
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| ADC Name |
EP4494710A2 Antibody-drug conjugate (3)
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| Synonyms |
EP4494710A2 Antibody-drug conjugate (3)
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| Organization |
DAIICHI SANKYO COMPANY | DAIICHI SANKYO EUROPE GMBH
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| Drug Status |
Investigative
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| Drug-to-Antibody Ratio |
4.9
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| Structure |
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| Antibody Name |
U1-59
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Antibody Info | ||||
| Antigen Name |
Receptor tyrosine-protein kinase erbB-3 (ERBB3)
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Antigen Info | ||||
| Payload Name |
EP4494710A2 Antibody-drug conjugate (1) Payload
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Payload Info | ||||
| Linker Name |
EP4494710A2 Antibody-drug conjugate (1) Linker
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Linker Info | ||||
ADC-specific functional property(2027 Update)
Binding Affinity
| Dissocation Constant (Kd) | Binding Target | Description | Reference |
|---|---|---|---|
| 1.653 nM |
HER3
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U1-59, the antibody-drug conjugate (3), the antibody-drug conjugate (10), or the antibody-drug conjugate (13) was evaluated as the antibody or the antibody-drug conjugates. The cells of each group were reacted with a primary antibody dilution for 45 minutes on ice and then washed with a FACS buffer. Further, 100uL of a FACS buffer or a reaction solution of a secondary antibody diluted 1/100 (phycoerythrin (PE)-coupled anti human antibody, Dianova GmbH #709-116-149) was added thereto. The cells were treated for 45 minutes on ice in the dark and then washed with a FACS buffer, and dead cells were excluded using a FACS buffer or a FACS buffer supplemented with 7-aminoactinomycin D (7AAD, Sigma-Aldrich Co. LLC, #A9400, 1.1 ug/mL). The equilibrium binding affinity (KD) and the maximum binding strength (Bmax) were calculated using GraphPad Prism software (version 5.04 for Windows (R) (one site-specific binding)).
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[1]
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References
