1 GlaxoSmithKline Medicines Research Centre, Stevenage, UK.
SLAS Discov. 2019 Sep;24(8):791-801. doi: 10.1177/2472555219859845.
During the past decade, the physicochemical quality of molecules under investigation at all stages of the drug discovery process has come under particular scrutiny. The issues associated with excessive lipophilicity and poor solubility in particular are many and varied, ranging from poor outcomes in screening campaigns to promiscuity, limited and/or poorly predictable pharmacokinetic exposure, and, ultimately, greater chances of clinical failure. In this review, contemporary methods to secure key measurements are described along with their relevance to understanding the behavior of molecules in environments pertinent to pharmacological activity. Together, the various measurements contribute to predictive models of both the physicochemical properties themselves and the outcomes they influence.
在过去的十年中,药物发现过程各个阶段研究分子的物理化学性质受到了特别关注。与过高的脂溶性和较差的水溶性相关的问题很多且多样,从筛选试验中的不良结果到混杂性、有限和/或难以预测的药代动力学暴露,最终导致临床失败的可能性增加。在这篇综述中,描述了确保关键测量的现代方法及其与理解与药理活性相关环境中分子行为的相关性。这些各种测量共同为物理化学性质本身及其影响的结果的预测模型做出了贡献。