目錄:MedChemExpress LLC>>信號通路>> S63845 | MedChemExpress (MCE)
CAS | 1799633-27-4 | 純度 | 99.94% |
---|---|---|---|
分子量 | 829.26 | 分子式 | C??H??ClF?N?O?S |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 10 mM * 1 mL |
貨號 | HY-100741 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 1799633-27-4
MCE 國際站:S63845
產(chǎn)品活性:S63845 是一種有效的選擇性骨髓細胞白血病 1 (MCL1) 抑制劑,結(jié)合人 MCL1 的 Kd 值為 0.19 nM。
研究領(lǐng)域:Apoptosis
作用靶點:Bcl-2 Family
In Vitro: The pro-survival protein myeloid cell leukemia 1 (MCL1) is over expressed in many cancers. S63845 is a small molecule that specifically binds with high affinity to the BH3-binding groove of MCL1. S63845 potently kills MCL1-dependent cancer cells, including multiple myeloma, leukaemia and lymphoma cells, by activating the BAX/BAK-dependent mitochondrial apoptotic pathway. The activity of S63845 is next evaluated in a panel of eight AML cell lines: all lines are sensitive to S63845 (IC50=4-233 nM).
In Vivo: S63845 shows potent anti-tumour activity with an acceptable safety margin as a single agent in several cancers. Intravenously injected (i.v.) S63845 exerts dose-dependent anti-tumour activity in human multiple myeloma (H929 and AMO1) xenografts in immunocompromised mice, with maximal tumour growth inhibition of 114% in the AMO1 model and 103% in the H929 model. At 25 mg/kg, S63845 induces complete regression in 7 out of 8 of the mice at 100 days after treatment in the AMO1 model.
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