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盐酸拓扑替康

品牌 厂商性质 产地 货期
阿拉丁 生产商 上海 现货

询价
产品参数
货号 CAS号 价格(元) 操作
T103153-10mg 119413-54-6 219 询价
T103153-50mg 119413-54-6 595 询价
产品介绍

  • 分子式 C23H24ClN3O5
  • 分子量457.91
  • Beilstein号
  • EC号
  • MDL号
  • PubChem编号

属性

熔点 213-218°C
存贮条件 2-8°C储存

描述

生化机理

Description:
IC50 Value: 37-280 uM (Human glioma cell lines) [1]
Topotecan (TPT, 9-dimethylaminomethyl-10-hydroxycamptothecin) is the first topoisomerase I-directed cytotoxic agent to enter clinical trials in the United States.
in vitro: Human glioma cell lines (U87, U138 and U373) displayed different sensitivities to topotecan (IC50range: 0.037 microM to 0.280 microM) in cell culture [1]. Examination of the IC50 values observed in colony-forming assays revealed that the CHRC5 cells were 15-fold (SD, +/- 3; n = 3) resistant to TPT after a 1-h exposure and 3.2-fold (SD, +/- 1.4; n = 4) resistant in continuous exposure experiments[2]. The DNA histograms at 4, 24, 48 and 72 h indicate that topotecan at IC80 concentrations causes accumulation of cells in S and G2/M phases, whereas gemcitabine at IC80 concentrations causes, accumulation of cells in G1 phase. Both compounds induced p53 and p21 expression in the H460 cell line but not in the H322 cell line [3]<

别名 盐酸拓扑特康;TPT (S)-10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-(H-Pyrano[3' , 4':6,7]indolizino[1,2-b]quinoline-3,14[4H,12H]-dione monohydrochloride 

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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