Medicinal Chemical Properties of Successful Central Nervous System Drugs

Hassan Pajouhesh Ph.D. , George R. Lenz
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引用次数: 1088

Abstract

Fundamental physiochemical features of CNS drugs are related to their ability to penetrate the blood-brain barrier affinity and exhibit CNS activity. Factors relevant to the success of CNS drugs are reviewed. CNS drugs show values of molecular weight, lipophilicity, and hydrogen bond donor and acceptor that in general have a smaller range than general therapeutics. Pharmacokinetic properties can be manipulated by the medicinal chemist to a significant extent. The solubility, permeability, metabolic stability, protein binding, and human ether-ago-go-related gene inhibition of CNS compounds need to be optimized simultaneously with potency, selectivity, and other biological parameters. The balance between optimizing the physiochemical and pharmacokinetic properties to make the best compromises in properties is critical for designing new drugs likely to penetrate the blood brain barrier and affect relevant biological systems. This review is intended as a guide to designing CNS therapeutic agents with better drug-like properties.

成功的中枢神经系统药物的药物化学性质
中枢神经系统药物的基本理化特性与其穿透血脑屏障的能力和中枢神经系统活性密切相关。本文综述了影响中枢神经系统药物成功的因素。中枢神经系统药物的分子量、亲脂性、氢键供体和受体的范围通常小于一般治疗药物。药物化学家可以在很大程度上操纵药代动力学性质。CNS化合物的溶解度、渗透性、代谢稳定性、蛋白质结合和人醚ago-go相关基因抑制需要与效价、选择性和其他生物学参数同时优化。在优化物理化学和药代动力学特性之间取得平衡,从而在特性上做出最佳妥协,对于设计可能穿透血脑屏障并影响相关生物系统的新药至关重要。本文综述旨在为设计具有更好的类药物特性的中枢神经系统治疗剂提供指导。
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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