CNS Drug Design: Balancing Physicochemical Properties for Optimal Brain Exposure 论文

2014Journal of Medicinal Chemistry引用 531
Pharmacogenetics and Drug MetabolismDrug Transport and Resistance MechanismsComputational Drug Discovery Methods

详细信息

发表期刊/会议
Journal of Medicinal Chemistry
发表日期
2014-12-11
发表年份
2014

关键词

Pharmacogenetics and Drug MetabolismDrug Transport and Resistance MechanismsComputational Drug Discovery Methods

摘要

The human brain is a uniquely complex organ, which has evolved a sophisticated protection system to prevent injury from external insults and toxins. Designing molecules that can overcome this protection system and achieve optimal concentration at the desired therapeutic target in the brain is a specific and major challenge for medicinal chemists working in CNS drug discovery. Analogous to the now widely accepted rule of 5 in the design of oral drugs, the physicochemical properties required for optimal brain exposure have been extensively studied in an attempt to similarly define the attributes of successful CNS drugs and drug candidates. This body of work is systematically reviewed here, with a particular emphasis on the interplay between the most critical physicochemical and pharmacokinetic parameters of CNS drugs as well as their impact on medicinal chemistry strategies toward molecules with optimal brain exposure. A summary of modern CNS pharmacokinetic concepts and methods is also provided.

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