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1290541-46-6

中文名稱 RAD51 INHIBITOR B02
英文名稱 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 2024/12/24 22:20:14
1290541-46-6 結(jié)構(gòu)式 1290541-46-6 結(jié)構(gòu)式

基本信息

中文別名
化合物B02
RAD51抑制劑(RAD51 INHIBITOR B02)
英文別名
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]-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)174-175o C
儲(chǔ)存條件2-8°C
溶解度二甲基亞砜:≥5mg/mL
形態(tài)粉末
顏色淡黃色至深黃色
穩(wěn)定性吸濕性

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類別碼22
WGK Germany3

常見(jiàn)問(wèn)題列表

生物活性
RAD51 Inhibitor B02 (B02)是人RAD51的抑制劑,IC50值為27.4 μM。
靶點(diǎn)

IC50: 27.4 μM (hRAD51)

體外研究

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.

體內(nèi)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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