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The dynamics of drug-target interactions: drug-target residence time and its impact on efficacy and safety

机译:药物-靶标相互作用的动力学:药物-靶标停留时间及其对功效和安全性的影响

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The extent and duration of pharmacological action is determined by the lifetime of drug occupancy on a molecular target. This lifetime is defined by dynamic processes that control the rates of drug association and dissociation from the target. Recently, the term residence time has been coined to describe experimental measurements that can be related to the lifetime of the binary drug-target complex, and this in turn to durable, pharmacody-namic activity. The residence time concept and its impact on drug optimization are reviewed here. Examples are provided that demonstrate how a long residence time can improve drug efficacy in vivo. Additionally, optimization of drug-target residence time can help to mitigate off-target mediated toxicity, hence, improving drug safety and tolerability. Recent applications of the residence time concept to both drug discovery and development are also presented.
机译:药理作用的程度和持续时间取决于药物在分子靶标上的寿命。该寿命由控制药物缔合和与靶标解离速率的动态过程定义。最近,创造了术语“停留时间”来描述实验测量结果,这些测量结果可能与二元药物靶标复合物的寿命有关,而这又与持久的药代动力学有关。本文对停留时间的概念及其对药物优化的影响进行了综述。提供的实例证明了长停留时间如何改善体内药物功效。另外,优化药物靶标停留时间可以帮助减轻靶标外介导的毒性,因此,改善了药物安全性和耐受性。还介绍了停留时间概念在药物发现和开发中的最新应用。

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