血浆蛋白和组织结合在药物发现项目中对成功交付临床前候选药物的重要性。

Q1 Pharmacology, Toxicology and Pharmaceutics Progress in medicinal chemistry Pub Date : 2022-01-01 Epub Date: 2022-06-06 DOI:10.1016/bs.pmch.2022.04.002
Elizabeth Hann, Karine Malagu, Andrew Stott, Huw Vater
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引用次数: 2

摘要

血浆蛋白结合和组织结合可以说是药物发现过程中测量的两个最关键的参数,因为根据游离药物假说,游离药物对疗效和毒性都有影响。本章旨在解构血浆蛋白和组织结合在药物发现程序中的作用,并考虑辉瑞和Genentech/Depomed十年前得出的结论,即优化血浆蛋白结合作为一个独立参数不会显著影响疗效。本章还将研究如何将结合指标应用于药物发现项目,并探索优化血浆蛋白或组织结合的情况,这是一种有效的策略,可以为临床前开发提供具有足够治疗指数的早期适应症的候选分子。
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The importance of plasma protein and tissue binding in a drug discovery program to successfully deliver a preclinical candidate.

Plasma protein binding and tissue binding are arguably two of the most critical parameters that are measured as part of a drug discovery program since, according to the free drug hypothesis, it is the free drug that is responsible for both efficacy and toxicity. This chapter aims to deconstruct the role of plasma protein and tissue binding in drug discovery programs, and to consider the conclusion made by Pfizer and Genentech/Depomed a decade ago that optimising plasma protein binding as an independent parameter does not significantly influence efficacy. This chapter will also examine how binding metrics are applied in drug discovery programs and explore circumstances where optimising plasma protein or tissue binding can be an effective strategy to deliver a candidate molecule for preclinical development with an early indication of sufficient therapeutic index.

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来源期刊
Progress in medicinal chemistry
Progress in medicinal chemistry Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
15.60
自引率
0.00%
发文量
6
期刊介绍: This series has a long established reputation for excellent coverage of almost every facet of Medicinal Chemistry and is one of the most respected and instructive sources of information on the subject. The latest volume certifies to the continuing success of a unique series reflecting current progress in a broadly developing field of science.
期刊最新文献
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