化合物 CS1 T60380

Product Introduction
Bioactivity


英文名: CS1

描述: CS1 是一种有效的DNA Topo II 抑制剂。CS1 显示出广谱的体外抗肿瘤作用、体内低毒性和潜在的抗多药耐药能力。CS1 导致 DNA 损伤、细胞周期停滞在 G2/M 期和细胞凋亡。

体外活性: CS1 has cytotoxicity with IC 50 values of 16.92 and 18.88 μM for MCF-7 and MCF7/ADR cells, respectively [1]. CS1 (10, 50, 100 μM) inhibits the topoisomerase II α (Topo IIα) activity [1]. CS1 (0-20 μM) shows antiproliferation activity in cancer cells [1]. CS1 (2.5, 5, 10 μM) induces cell cycle arrest at the G2/M phase [1]. CS1 (2.5, 5, 10 μM) induces cell apoptosis [1]. CS1 (5, 10, 15 μM; 24 h) induces DNA breaks in MDA-MB-231 cells [1]. Cell Cycle Analysis [1] Cell Line: MDA-MB-231 cells Concentration: 2.5, 5, 10 μM Incubation Time: Result: Cells were arrest at the G2/M phase. Apoptosis Analysis [1] Cell Line: MDA-MB-231 cells Concentration: 2.5, 5, 10 μM Incubation Time: Result: Induced apoptosis

体内活性: CS1 (20 mg/kg; i.v.; every other day for two weeks) has antitumor effects [1]. Animal Model: Five-week-old female athymic nude mice (BALB/c-nu) [1] Dosage: 20 mg/kg Administration: i.v., every other day for two weeks Result: Showed antitumor effects.

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

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注：该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案，不可用于临床诊断或治疗等相关用途