An update on lipophilic efficiency as an important metric in drug design.

IF 6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Expert Opinion on Drug Discovery Pub Date : 2024-08-01 Epub Date: 2024-06-26 DOI:10.1080/17460441.2024.2368744
Rebecca A Gallego, Martin P Edwards, T Patrick Montgomery
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引用次数: 0

Abstract

Introduction: Lipophilic efficiency (LipE) and lipophilic metabolic efficiency (LipMetE) are valuable tools that can be utilized as part of a multiparameter optimization process to advance a hit to a clinical quality compound.

Areas covered: This review covers recent, effective use cases of LipE and LipMetE that have been published in the literature over the past 5 years. These use cases resulted in the delivery of high-quality molecules that were brought forward to in vivo work and/or to clinical studies. The authors discuss best-practices for using LipE and LipMetE analysis, combined with lipophilicity-focused compound design strategies, to increase the speed and effectiveness of the hit to clinical quality compound optimization process.

Expert opinion: It has become well established that increasing LipE and LipMetE within a series of analogs facilitates the improvement of broad selectivity, clearance, solubility, and permeability and, through this optimization, also facilitates the achievement of desired pharmacokinetic properties, efficacy, and tolerability. Within this article, we discuss lipophilic efficiency-focused optimization as a tool to yield high-quality potential clinical candidates. It is suggested that LipE/LipMetE-focused optimization can facilitate and accelerate the drug-discovery process.

亲脂效率作为药物设计重要指标的最新进展。
简介:亲脂效率(LipE)和亲脂代谢效率(LipMetE)是非常有价值的工具,可作为多参数优化过程的一部分,将命中化合物提升为临床优质化合物:本综述涵盖过去 5 年文献中发表的 LipE 和 LipMetE 的最新有效用例。这些使用案例产生了高质量的分子,并将其用于体内工作和/或临床研究。作者讨论了使用 LipE 和 LipMetE 分析的最佳实践,结合以亲油性为重点的化合物设计策略,以提高从命中到临床优质化合物优化过程的速度和有效性:在一系列类似物中增加 LipE 和 LipMetE 有助于提高广泛的选择性、清除率、溶解度和渗透性,而且通过这种优化,还有助于实现理想的药代动力学特性、疗效和耐受性,这一点已得到公认。在这篇文章中,我们讨论了以亲脂效率为重点的优化,将其作为一种工具来产生高质量的潜在临床候选药物。我们认为,以 LipE/LipMetE 为重点的优化可以促进和加快药物发现过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.20
自引率
1.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Drug Discovery (ISSN 1746-0441 [print], 1746-045X [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on novel technologies involved in the drug discovery process, leading to new leads and reduced attrition rates. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering chemoinformatics; bioinformatics; assay development; novel screening technologies; in vitro/in vivo models; structure-based drug design; systems biology Drug Case Histories examining the steps involved in the preclinical and clinical development of a particular drug The audience consists of scientists and managers in the healthcare and pharmaceutical industry, academic pharmaceutical scientists and other closely related professionals looking to enhance the success of their drug candidates through optimisation at the preclinical level.
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