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Idarubicin HCl
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
货号 | CAS号 | 操作 |
---|---|---|
I129863-10mg | 57852-57-0 | 询底价 |
I129863-1mg | 57852-57-0 | 询底价 |
I129863-50mg | 57852-57-0 | 询底价 |
I129863-5mg | 57852-57-0 | 询底价 |
产品介绍
- 分子式 C26H27NO9·HCl
- 分子量533.95
- Beilstein号
- EC号 MFCD00866457
- MDL号 260-990-7
- PubChem编号
属性
溶解性 | DMSO 100 mg/mL (187.28 mM);Water 7 mg/mL heating (13.1 mM);Ethanol <1 mg/mL (<1 mM) |
存贮条件 | 储存温度-20°C |
描述
应用 | An apoptosis inducer. |
产品介绍 | Idarubicin HCl是Idarubicin的盐酸盐形式,是蒽环类抗生素,抑制DNA拓扑异构酶II (topo II),作用于MCF-7细胞,IC50为3.3 ng/mL。 |
备注 | Idarubicin HCl is a hydrochloride salt form of Idarubicin which is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3 ng/mL. |
生化机理 | Idarubicin Hydrochloride is the hydrochloride salt preparation of Idarubicin (IDA), an anthracycline and an analog of daunorubicin. IDA is rapidly metabolized to its 13-dihydroderivative (Idarubicinol) which is more stable than the parent form. This compound has been reported to trigger apoptotic cell death via enhancement of Fas and caspase-3/caspase-7 expression. In experiments, where cells were exposed to IDA, reactive oxygen species (ROS) were produced which induced DNA strand breaks and prevented DNA polymerase reaction. Idarubicin Hydrochloride is an inhibitor of Topo II α. Idarubicin Hydrochloride is also a substrate of CYP2D6 and CYP2C9. |
别名 | 盐酸依达比星; 去甲氧基柔红霉素盐酸盐;Idamycin;Zavedos;4-demethoxydaunorubicin;Idamycin;Zavedos;4-demethoxydaunorubicin;(7S-cis)-9-Acetyl-7-[(3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-5,12-naphthacenedione hydrochloride |
Idarubicin HCl信息由上海阿拉丁生化科技股份有限公司为您提供,如您想了解更多关于Idarubicin HCl报价、型号、参数等信息,欢迎来电或留言咨询。
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