亲脂性
药品
药物发现
化学
药理学
立体化学
生物化学
医学
作者
John A. Arnott,Sonia Lobo Planey
标识
DOI:10.1517/17460441.2012.714363
摘要
A current review of the literature reveals a continued reliance on the synthesis of novel structures with increased potency, rather than a focus on maintaining optimal physicochemical properties associated with ADMET throughout drug optimization. Particular attention to the optimum region of lipophilicity, as well as monitoring of lipophilic efficiency indices, may contribute significantly to the overall quality of candidate drugs at different stages of discovery.
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