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醛氧化酶介导的类药物分子代谢:一项计算与实验相结合的研究

Aldehyde Oxidase Mediated Metabolism in Drug-like Molecules: A Combined Computational and Experimental Study.

作者信息

Xu Yuan, Li Liang, Wang Yulan, Xing Jing, Zhou Lei, Zhong Dafang, Luo Xiaomin, Jiang Hualiang, Chen Kaixian, Zheng Mingyue, Deng Pan, Chen Xiaoyan

机构信息

Shanghai Institute of Materia Medica, Chinese Academy of Sciences , Shanghai 201203, China.

University of Chinese Academy of Sciences , No. 19A Yuquan Road, Beijing 100049, China.

出版信息

J Med Chem. 2017 Apr 13;60(7):2973-2982. doi: 10.1021/acs.jmedchem.7b00019. Epub 2017 Mar 16.

Abstract

Aldehyde oxidase (AOX) is an important drug-metabolizing enzyme. However, the current in vitro models for evaluating AOX metabolism are sometimes misleading, and preclinical animal models generally fail to predict human AOX-mediated metabolism. In this study, we report a combined computational and experimental investigation of drug-like molecules that are potential aldehyde oxidase substrates, of which multiple sites of metabolism (SOMs) mediated by AOX and their preferences for the reaction can be unambiguously identified. In addition, the proposed strategy was used to evaluate the metabolism of newly designed c-Met inhibitors, and a success switch-off of AOX metabolism was observed. Overall, this study provide useful information to guide lead optimization and drug discovery based on AOX-mediated metabolism.

摘要

醛氧化酶(AOX)是一种重要的药物代谢酶。然而,目前用于评估AOX代谢的体外模型有时会产生误导,临床前动物模型通常无法预测人类AOX介导的代谢。在本研究中,我们报告了对潜在醛氧化酶底物的类药物分子进行的计算与实验相结合的研究,通过该研究可以明确识别由AOX介导的多个代谢位点(SOMs)及其对反应的偏好。此外,所提出的策略用于评估新设计的c-Met抑制剂的代谢,并观察到AOX代谢的成功关闭。总体而言,本研究为基于AOX介导的代谢来指导先导化合物优化和药物发现提供了有用信息。

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