Duocarmycin SA

Duocarmycin SA is an extremely potent cytotoxic agent and antitumor antibiotic that induces sequence-selective alkylation of duplex DNA, with an IC50 of 10 pM. It demonstrates synergistic cytotoxicity against glioblastoma multiforme (GBM) cells when combined with proton radiation in vitro.

Seco-Duocarmycin SA is a highly potent DNA alkylator used as an ADC cytotoxin.

Mal-PEG4-VC-PAB-DMEA-Seco-Duocarmycin SA is an antibody-drug conjugate linker that incorporates the antitumor antibiotic Duocarmycin SA, connected through the Mal-PEG4-VC-PAB-DMEA-Seco linker, for targeted cancer therapy.

Mal-PEG4-VC-PAB-DMEA-duocarmycin SA 是一种硫醇反应型 Drug-linker,duocarmycin SA 是一种非常有效的、具有口服活性的细胞毒性剂，可用于抗体-药物偶联物（ADC）的合成。

DBCO-PEG4-VC-PAB-DMEA-Duocarmycin SA 是一种是一种点击反应型 Drug-linker，含有 DBCO 基团，可以和含有 Azide 基团的分子发生环张力 (strain) 促进的炔-叠氮环加成反应 (SPAAC)。duocarmycin SA 是一种非常有效的、具有口服活性的细胞毒性剂，DBCO-PEG4-VC-PAB-DMEA-Duocarmycin SA可用于抗体-药物偶联物（ADC）的合成。

(S)-Seco-Duocarmycin SA 是一种 DNA 烷化剂，也是具有高效抗肿瘤活性的抗生素，可用于合成 ADC 化合物。