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1146702-54-6

中文名称 CAL-101
英文名称 CAL-101
CAS 1146702-54-6
分子式 C22H18FN7O
分子量 415.423
MOL 文件 1146702-54-6.mol
更新日期 2024/05/20 09:19:54
1146702-54-6 结构式 1146702-54-6 结构式

基本信息

中文别名
艾代拉里斯杂质
艾代拉里斯杂质A
英文别名
Idelalisib
GS-1101, Idelalisib
CAL-101 (GS-1101, Idelalisib)
5-fluoro-3-phenyl-2-((1s)-1-(1h-purin-6-ylamino)ethyl)-4(3h)...

应用领域

用途一
Idelalisib is an orally available selective and potent phosphatidylinositol 3-kinase δ (PI3 Kδ) inhibitor originally developed by Calistoga Pharmaceuticals, which was acquired by Gilead in April 2014. In July 2014, the drug was approved in the USA for the treatment of relapsed chronic lymphocytic leukemia as well as several oncology orphan drug designations. Since idelalisib specifically inhibits PI3Kd, which is expressed primarily in bloodcell lineages, the therapeutic effect is localized, limiting interference with PI3K isoform signaling that is critical to normal function of healthy cells.

常见问题列表

生物活性
CAL-101是一种有效的选择性的p110δ抑制剂,IC50为2.5nM,比作用于其他I类PI3K酶(抑制p110α,p110β和p110γ;IC50分别为820,565和89nM)选择性高40到300倍。
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