Department of Pharmaceutical Sciences, Southern Illinois University Edwardsville, Edwardsville, Illinois 62026, United States.
Curr Med Chem. 2018;25(28):3353-3373. doi: 10.2174/0929867325666180226104126.
Cytochrome P450s are enzymes capable of metabolizing a wide variety of drugs. Their significant impact in drug discovery has led to extensive research, computationally and experimentally, in order to explore how a chemical entity responds to metabolizing enzymes. We present an overview of ligand-based and structure-based methodologies, along with pertinent information on the structures, biology, and relevance of these enzymes.
细胞色素 P450 是能够代谢多种药物的酶。它们在药物发现中的重要影响导致了广泛的计算和实验研究,以探索化学实体如何响应代谢酶。我们介绍了基于配体和基于结构的方法学的概述,以及这些酶的结构、生物学和相关性的相关信息。