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CH5132799 (PA-799)

编号: 160926015
Cas号: 1007207-67-1
纯度: 98% by HPLC 

CH5132799, also known as PA-799, is a novel class I PI3K inhibitor, which exhibited a strong inhibitory activity especially against PI3K (IC(50)=0.014 M). In human tumor cell lines with PI3K pathway activation, CH5132799 showed potent antiproliferative activity. CH5132799 is orally available and showed significant antitumor activity in PI3K pathway-activated human cancer xenograft models in mice. CH5132799 selectively inhibited class I PI3Ks and PI3K mutants in in vitro kinase assays. Tumors harboring PIK3CA mutations were significantly sensitive to CH5132799 in vitro and were remarkably regressed by CH5132799 in in vivo mouse xenograft models. 

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化学信息

名称CH5132799 (PA-799)
Iupac 化学名称5-(7-(methylsulfonyl)-2-morpholino-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine 
同义词CH5132799; CH-5132799; CH 5132799; PA-799; PA799; PA-799. 
英文同义词CH5132799; CH-5132799; CH 5132799; PA-799; PA799; PA-799. 
分子式C15H19N7O3S 
分子量377.42146 
SmileCS(=O)(=O)N1CCC2=C1N=C(N=C2C=2C=NC(=NC2)N)N2CCOCC2
InChiKeyJEGHXKRHKHPBJD-UHFFFAOYSA-N
InChiInChI=1S/C15H19N7O3S/c1-26(23,24)22-3-2-11-12(10-8-17-14(16)18-9-10)19-15(20-13(11)22)21-4-6-25-7-5-21/h8-9H,2-7H2,1H3,(H2,16,17,18)
Cas号1007207-67-1
相关CAS号

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外观性状Solid powder 
纯度98% by HPLC 
存储-20 ºC for 3 years 
可溶性Soluble in DMSO 
处理方式
运输条件Shipped under ambient temperature 
海关编码
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Targets
Mechanism
Cell study
Animal study
Clinical study
Not available

化学结构

160926015 - CH5132799 (PA-799) | CAS 1007207-67-1

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