Examining the Chirality, Conformation and Selective Kinase Inhibition of 3-((3R,4R)-4-methyl-3-(methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)piperidin-1-yl)-3-oxopropanenitrile (C
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- 作者：Jian-kang Jiang ; Kamran Ghoreschi ; Francesca Deflorian ; Zhi Chen ; Melissa Perreira ; Marko Pesu ; Jeremy Smith ; Dac-Trung Nguyen ; Eric H. Liu ; William Leister ; Stefano Costanzi ; John J. O’ ; Shea ; Cra
- 刊名：Journal of Medicinal Chemistry
- 出版年：2008
- 出版时间：December 25, 2008
- 年：2008
- 卷：51
- 期：24
- 页码：8012-8018
- 全文大小：271K
- 年卷期：v.51,no.24(December 25, 2008)
- ISSN：1520-4804
文摘
Here, we examine the significance that stereochemistry plays within the clinically relevant Janus kinase 3 (Jak3) inhibitor 1 (CP-690,550). A synthesis of all four enantiopure stereoisomers of the drug was carried out and an examination of each compound revealed that only the enantiopure 3R,4R isomer was capable of blocking Stat5 phosphorylation (Jak3 dependent). Each compound was profiled across a panel of over 350 kinases, which revealed a high level of selectivity for the Jak family kinases for these related compounds. Each stereoisomer retained a degree of binding to Jak3 and Jak2 and the 3R,4S and 3S,4R stereoisomers were further revealed to have binding affinity for selected members of the STE7 and STE20 subfamily of kinases. Finally, an appraisal of the minimum energy conformation of each stereoisomer and molecular docking at Jak3 was performed in an effort to better understand each compounds selectivity and potency profiles.