羧酸酯酶
前药
酰胺
结合位点
水解
化学
立体化学
酶
组合化学
生物化学
作者
Huiying Chu,Hanyi Min,Mingbo Zhang,Hujun Shen,Guohui Li
标识
DOI:10.2174/15680266113139990009
摘要
Human carboxylesterase I (hCES 1) plays an important role in the metabolism and activation of prodrugs, such as, the hydrolysis of a variety of drugs of prodrugs featuring an ester, amide or carbamate function. The bindings of the substrates of different lengths and cocaine to hCES1 at two different binding sites, catalytic site and Z-site, were studies through MD simulations. For each case, the correlation analysis has been performed to explore the binding patterns of a broad range of substrates binding to the hCES1. Keywords: hCES1, binding pattern, molecular simulations.
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