化学
电泳剂
配体(生物化学)
效力
反应性(心理学)
共价键
立体化学
组合化学
化学合成
结构-活动关系
配体效率
共价结合
作者
Benjamin D. Horning,Cian Kingston,Gabriel M. Simon,Matthew P. Patricelli,David S. Weinstein,Brian N. Cook
标识
DOI:10.1021/acs.jmedchem.5c01803
摘要
High Resolution Image Download MS PowerPoint Slide Covalent modalities represent an important component of the modern medicinal chemist’s toolbox for pursuing challenging targets in drug discovery. By taking a “covalent-first” approach to identifying druggable pockets on challenging-to-drug targets, we and others have expanded accessible target space and driven fragment-like hits to clinical-stage molecules. The field has long recognized intrinsic warhead reactivity as a key parameter to monitor, typically addressed by determining k inact and K I values, which are impractically time-intensive and can be misleading regarding reactivity. Here we present an alternative way to normalize potency for electrophilicity utilizing glutathione (GSH) consumption data, which enables us to extract target-specific improvements in potency, a metric we term ligand reactivity efficiency (LRE). Our hope is that the details of our approach and this metric will simplify the rational design of covalent drugs for fellow practitioners in the field.
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