香豆素
化学
羧酸盐
呋喃
丝氨酸
公共化学
对接(动物)
立体化学
组合化学
生物化学
有机化学
酶
医学
护理部
作者
Ahmad J. Obaidullah,Rami A. Al‐Horani
出处
期刊:Cardiovascular and Hematological Agents in Medicinal Chemistry
[Bentham Science]
日期:2017-11-08
卷期号:15 (1)
被引量:12
标识
DOI:10.2174/1871525715666170529093938
摘要
Direct inhibition of coagulation factor XIa (FXIa) carries a significant promise for developing effective and safe anticoagulants.In this report, we studied 4-methyl-2-oxo-2H-chromen-7-yl furan-2-carboxylate 1, a coumarin derivative, for direct FXIa inhibition.This small molecule was found to inhibit FXIa with an IC50 value of 0.77 µM. Coumarin 1 also displayed a moderate-to-high selectivity for FXIa inhibition over other coagulation, digestive, and fibrinolysis serine proteases. Coumarin 1 selectively doubled APTT of human plasma at a concentration of 72 µM. Insights about the structural features that contribute to the unique potential of such small molecule were deduced by profiling similar molecules in PubChem Open Chemistry Database as well as by performing a computational docking exercise.Overall, chromen-7-yl furan-2-carboxylate 1 is expected to serve as an excellent fragmental lead for further anticoagulant design and development.
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