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Duocarmycin 是一种 DNA 小沟烷化剂,是一种抗体药物偶联物 (ADC) 毒素。 Duocarmycin 基于其特有的弯曲吲哚结构和螺环丙基环己二烯酮亲电体发挥抗癌活性。
Duocarmycin is based on its characteristic curved indole structure and a spirocyclopropylcyclohexadienone electrophile to act anticancer activity. Duocarmycin is a DNA minor groove binding alkylating agent and explored as drug-antibody conjugates (ADCs) [1].
[1]. Koch MF, et al. Structural, Biochemical, and Computational Studies Reveal the Mechanism of Selective Aldehyde Dehydrogenase 1A1 Inhibition by Cytotoxic Duocarmycin Analogues. Angew Chem Int Ed Engl. 2015 Nov 9;54(46):13550-4.
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