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1290541-46-6

中文名称 RAD51 INHIBITOR B02
英文名称 3-(Phenylmethyl)-2-[(1E)-2-(3-pyridinyl)ethenyl]-4(3H)-quinazolinone
CAS 1290541-46-6
分子式 C22H17N3O
分子量 339.39
MOL 文件 1290541-46-6.mol
更新日期 2024/04/27 11:50:39
1290541-46-6 结构式 1290541-46-6 结构式

基本信息

中文别名
化合物B02
RAD51抑制剂(RAD51 INHIBITOR B02)
英文别名
BO2
B02
CS-2461
RAD51 Inhibitor B02
RAD51 Inhibitor B02 >=98% (HPLC)
RAD51 Inhibitor, B02 - CAS 1290541-46-6 - Calbiochem
(E)-3-benzyl-2-(2-(pyridin-3-yl)vinyl)quinazolin-4(3H)-one
3-(Phenylmethyl)-2-[(1E)-2-(3-pyridinyl)ethenyl]-4(3H)-quinazolinone
4(3H)-Quinazolinone, 3-(phenylmethyl)-2-[(1E)-2-(3-pyridinyl)ethenyl]-
所属类别
生物化工:激动剂抑制剂

物理化学性质

熔点174-175o C
储存条件2-8°C
溶解度二甲基亚砜:≥5mg/mL
形态粉末
颜色淡黄色至深黄色
稳定性吸湿性

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302
危险品标志Xn
危险类别码22
WGK Germany3

常见问题列表

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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