住所
停留时间(流体动力学)
背景(考古学)
药物发现
药品
药物开发
药代动力学
药效学
药理学
医学
生物信息学
生物
人口学
工程类
社会学
古生物学
岩土工程
标识
DOI:10.1016/j.drudis.2017.07.016
摘要
Since the importance of drug target residence time was first highlighted more 10 years ago, slow binding kinetics has received much attention in the drug discovery literature, and indeed within pharmaceutical research. However, the residence concept as presented in most papers is supported by rather misleading simulations and arguments, and by examples where compounds are taken out of their pharmacokinetic context. Moreover, fast association is typically more desirable than slow, and advantages of long residence time, notably a potential disconnect between pharmacodynamics (PD) and pharmacokinetics (PK), would be partially or completely offset by slow on-rate. Therefore, plain potency is likely a better predictor of drug development success than is residence time.
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