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GSK2636771

编号: 52618
Cas号: 1372540-25-4
纯度: 98% by HPLC 

GSK2636771 is a potent, orally bioavailable and selective inhibitor of PI3K (0.89 nM), with >900-fold selectivity over PI3K/PI3K and >10-fold over PI3K. It inhibits AKT phosphorylation and downstream signalling measured as decrease of PRAS40-, GSK3-, and RPS6-phosphorylation in PTEN mutant cell lines.

 

仅供研究使用。 我们不向患者出售。

化学信息

名称GSK2636771
Iupac 化学名称2-methyl-1-(2-methyl-3-(trifluoromethyl)benzyl)-6-morpholino-1H-benzo[d]imidazole-4-carboxylic acid 
同义词GSK-2636771,GSK 2636771 
英文同义词GSK-2636771,GSK 2636771 
分子式C22H22F3N3O3 
分子量433.42 
SmileCC1=NC2=C(N1CC1=C(C(=CC=C1)C(F)(F)F)C)C=C(C=C2C(=O)O)N2CCOCC2
InChiKeyXTKLTGBKIDQGQL-UHFFFAOYSA-N
InChiInChI=1S/C22H22F3N3O3/c1-13-15(4-3-5-18(13)22(23,24)25)12-28-14(2)26-20-17(21(29)30)10-16(11-19(20)28)27-6-8-31-9-7-27/h3-5,10-11H,6-9,12H2,1-2H3,(H,29,30)
Cas号1372540-25-4
相关CAS号

订购信息

包装价格库存纯度备货期
大货询价询价询价
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外观性状solid 
纯度98% by HPLC 
存储3 years -20ºCpowder 
可溶性Soluble in DMSO 
处理方式
运输条件Shipped under ambient temperature as non-hazardous chemical. 
海关编码
Coming soon.
Targets
Mechanism
Cell study
Animal study
Clinical study
Not available

化学结构

52618 - GSK2636771 | CAS 1372540-25-4

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