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酶抑制作用的评估:以单胺氧化酶和胆碱酯酶抑制药物开发为例的综述

Assessment of Enzyme Inhibition: A Review with Examples from the Development of Monoamine Oxidase and Cholinesterase Inhibitory Drugs.

作者信息

Ramsay Rona R, Tipton Keith F

机构信息

Biomedical Sciences Research Complex, University of St Andrews, St Andrews KY16 8QP, UK.

School of Biochemistry and Immunology, Trinity College, Dublin 2, Ireland.

出版信息

Molecules. 2017 Jul 15;22(7):1192. doi: 10.3390/molecules22071192.

Abstract

The actions of many drugs involve enzyme inhibition. This is exemplified by the inhibitors of monoamine oxidases (MAO) and the cholinsterases (ChE) that have been used for several pharmacological purposes. This review describes key principles and approaches for the reliable determination of enzyme activities and inhibition as well as some of the methods that are in current use for such studies with these two enzymes. Their applicability and potential pitfalls arising from their inappropriate use are discussed. Since inhibitor potency is frequently assessed in terms of the quantity necessary to give 50% inhibition (the IC value), the relationships between this and the mode of inhibition is also considered, in terms of the misleading information that it may provide. Incorporation of more than one functionality into the same molecule to give a multi-target-directed ligands (MTDLs) requires careful assessment to ensure that the specific target effects are not significantly altered and that the kinetic behavior remains as favourable with the MTDL as it does with the individual components. Such factors will be considered in terms of recently developed MTDLs that combine MAO and ChE inhibitory functions.

摘要

许多药物的作用都涉及酶抑制。单胺氧化酶(MAO)和胆碱酯酶(ChE)抑制剂已被用于多种药理学目的,这便是例证。本综述描述了可靠测定酶活性和抑制作用的关键原理与方法,以及当前用于这两种酶此类研究的一些方法。讨论了它们的适用性以及因使用不当而产生的潜在问题。由于抑制剂效力通常根据产生50%抑制所需的量(IC值)来评估,因此还考虑了IC值与抑制模式之间的关系,以及它可能提供的误导性信息。将不止一种功能基团引入同一分子以得到多靶点导向配体(MTDL)需要仔细评估,以确保特定靶点效应不会显著改变,并且MTDL的动力学行为与单个组分一样有利。将结合MAO和ChE抑制功能的最新开发的MTDL纳入考虑,将会探讨这些因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8c/6152246/2d7d3034342d/molecules-22-01192-g001.jpg

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