cyp2j2模板体系的构建及其在配体代谢预测中的应用

Food safety (Tokyo, Japan) Pub Date : 2024-12-20 eCollection Date: 2024-12-01 DOI:10.14252/foodsafetyfscj.D-24-00010
Yasushi Yamazoe, Norie Murayama
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引用次数: 0

摘要

从配体的组装出发,引入了与其他人类CYP1A1、CYP1A2、CYP2B6、CYP2C8、CYP2C9、CYP2C18、CYP2C19、CYP2E1、CYP3A4、CYP3A5和CYP3A7的模板系统相同的允许宽度、触发残基和残基引发的配体在活性位点的运动等思想,构建了一个用于理解人类cyp2j2介导反应的模板系统(Drug Metab Pharmacokinet 2016、2017、2019、2020、2021、2022、2023、2024、2024年出版)。CYP2J2系统还包括模板上配体双分子结合的思想。根据它们在模板上的位置和相互作用模式的规则,对这些配体进行了良好和不良底物、区域/立体选择性和抑制相互作用的验证。因此,改进的CYP2J2-Template系统将提供可靠的估计,这种人类CYP对不同结构配体的催化作用,以及它们的解码信息,从而导致判断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of a CYP2J2-Template System and Its Application for Ligand Metabolism Prediction.

A Template system for the understanding of human CYP2J2-mediated reactions was constructed from the assembly of the ligands with the introduction of ideas of allowable width, Trigger-residue and the residue-initiated movement of ligands in the active site, which were in common with other Template* systems for human CYP1A1, CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C18, CYP2C19, CYP2E1, CYP3A4, CYP3A5, and CYP3A7 (Drug Metab Pharmacokinet 2016, 2017, 2019, 2020, 2021, 2022, 2023, 2024, and in press 2024). CYP2J2 system also includes ideas of bi-molecule binding of ligands on the Template. From their placements on the Template and rules for interaction modes, verifications of good and poor substrates, regio/stereo-selectivity, and inhibitory interaction became available faithfully for these ligands. The refined CYP2J2-Template system will thus offer reliable estimations of this human CYP catalysis toward ligands of diverse structures, together with their deciphering information to lead to judgments.

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