生物活性 靶点 体外研究 体内研究 RAD51 INHIBITOR B02 试剂级价格
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RAD51 INHIBITOR B02

RAD51 INHIBITOR B02,1290541-46-6,结构式
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
RAD51 INHIBITOR B02化学性质
  • 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
安全信息
  • 危险品标志 :Xn
  • 危险类别码 :22
  • WGK Germany :3

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。
  • 靶点

    IC50: 27.4 μM (hRAD51)

  • 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.

  • 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.

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RAD51 INHIBITOR B02 试剂级价格
  • 更新日期:2024/04/30
  • 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:2024/04/30
  • 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
RAD51 INHIBITOR B02生产厂家
  • 公司名称:上海与昂化工有限公司
  • 联系电话:021-021-58111628 15800915896
  • 电子邮件:sales@twochem.com
  • 国家:中国
  • 产品数:304
  • 优势度:55