Mc-MMAE 是保护基团 (马来酰亚氨基己酰) 共轭连接到单甲基 auristatin E (MMAE)。Mc-MMAE 是有效的微管蛋白抑制剂,是抗体偶联药物 (ADC) 中的毒性物质。
Description | Mc-MMAE is a protective group (maleimidocaproyl)-conjugated monomethyl auristatin E (MMAE), which is a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate (ADC). | ||||||||||||||||
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IC50 & Target | Tubulin, Antibody-drug conjugates (ADC)[1] | ||||||||||||||||
In Vitro | Synthesis of maleimidocaproyl-MMAE (mc-MMAE) requires the addition of maleimidocaproic acid to a solution of MMAE in dichloromethane followed by the addition of diethyl cyanophosphonate and diisopropylethylamine[1]. | ||||||||||||||||
Solvent & Solubility | In Vitro: DMSO : ≥ 51 mg/mL (55.97 mM) * "≥" means soluble, but saturation unknown. Preparing Stock Solutions
* Please refer to the solubility information to select the appropriate solvent. | ||||||||||||||||
References |
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