DM3-SMe 是一种美登素衍生物,是一种微管蛋白 (tubulin) 抑制剂,是一种抗体-药物偶联物 (ADCs) 的细胞毒性部分,可通过二硫键或稳定的硫醚键与抗体连接。DM3-SMe 在体外显示出高度的细胞毒性活性,IC50 为 0.0011 nM。
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DM3-SMe is a maytansine derivative and a tubulin inhibitor, and is a cytotoxic moiety of antibody-drug conjugates (ADCs), which can be linked to antibody through disulfide bond or stable thioether bond. DM3-SMe shows highly cytotoxic activity in vitro with an IC50 of 0.0011 nM[1][2].
[1]. Chen H, et al. Tubulin Inhibitor-Based Antibody-Drug Conjugates for Cancer Therapy. Molecules. 2017 Aug 1;22(8). [2]. Yuliang Zhaoet al. Biomedical Nanomaterials. 2016-?Science.
Fosbretabulin (Combretastatin A4 Phosphate (CA4P)) Disodium
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