RAD51 INHIBITOR B02
- CAS号:1290541-46-6
- 英文名:3-(Phenylmethyl)-2-[(1E)-2-(3-pyridinyl)ethenyl]-4(3H)-quinazolinone
- 中文名:RAD51 INHIBITOR B02
- CBNumber:CB82751056
- 分子式:C22H17N3O
- 分子量:339.39
- MOL File:1290541-46-6.mol
- 熔点 :174-175o C
- 储存条件 :2-8°C
- 溶解度 :DMSO: ≥5mg/mL
- 形态 :powder
- 颜色 :faint yellow to dark yellow
- 稳定性 :Hygroscopic
RAD51 INHIBITOR B02性质、用途与生产工艺
- 生物活性 RAD51 Inhibitor B02 (B02)是人RAD51的抑制剂,IC50值为27.4 μM。
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靶点
IC50: 27.4 μM (hRAD51)
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体外研究
RAD51 Inhibitor B02 specifically inhibits human RAD51 (IC 50 =27.4 μM), but not its E. coli homologue RecA (IC 50 >250 μM). The combination of B02 with cisplatin has the strongest killing effect on the human breast cancer cells MDA-MB-231.
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体内研究
B02 significantly enhances the therapeutic effect of cisplatin on tumor cells in vivo . B02 is tolerated by mice at doses up to 50 mg/kg without obvious body weight loss. No inhibition of tumor growth is observed on mice solely treated by B02. Mice treated with 4 mg/kg cisplatin, however, shows a 33% inhibition of tumor growth. Finally, mice treated with 50 mg/kg B02 and 4 mg/kg cisplatin shows a 66% inhibition of tumor growth.
- 更新日期:2024/11/08
- 产品编号:HY-101462
- 产品名称:RAD51 Inhibitor B02
- CAS编号:
- 包装:1 mg
- 价格:308元
- 更新日期:2024/11/08
- 产品编号:HY-101462
- 产品名称:RAD51 INHIBITOR B02 RAD51 Inhibitor B02
- CAS编号:1290541-46-6
- 包装:5mg
- 价格:770元
- 公司名称:TOCRIS-US
- 联系电话:--
- 电子邮件:customerservice@tocris.co.uk
- 国家:英国
- 产品数:5726
- 优势度:77