Viarengo-Baker Lauren A, Whitty Adrian
Relay Therapeutics, 399 Binney Street, Cambridge, Massachusetts 02139, United States.
J Med Chem. 2025 Aug 14;68(15):15260-15284. doi: 10.1021/acs.jmedchem.4c02886. Epub 2025 Jul 31.
Macrocycles are emerging as a prominent modality in drug discovery, including for conventionally druggable targets for which simpler, acyclic ligands are readily discoverable. Given the additional synthetic challenges associated with macrocyclic chemotypes, we address what benefits macrocycles provided for these highly druggable targets. To do this, we examine the effects of macrocyclization on inhibitors of highly druggable kinase targets. For each example, we isolate closely matched acyclic/macrocyclic compound pairs, allowing us to pinpoint the effects of macrocyclization on binding affinity, selectivity, and ADME properties absent confounding factors. Our findings show that while the impact of macrocyclization on potency is variable, a profound effect on selectivity is common. Macrocyclization can also bring benefits for membrane permeability, efflux ratio, blood-brain barrier penetrance, and metabolic stability. These findings lead us to propose specific circumstances in which a drug discoverer targeting kinases or other conventionally druggable target classes should consider a macrocycle approach.
大环化合物正在成为药物发现中的一种突出模式,包括针对那些传统上易于成药的靶点,对于这些靶点而言,更容易发现结构简单的非环状配体。鉴于与大环化学类型相关的额外合成挑战,我们探讨了大环化合物为这些高度易于成药的靶点带来了哪些益处。为此,我们研究了大环化对高度易于成药的激酶靶点抑制剂的影响。对于每个例子,我们分离出紧密匹配的非环状/大环化合物对,这使我们能够在没有混杂因素的情况下,精准确定大环化对结合亲和力、选择性和药代动力学性质的影响。我们的研究结果表明,虽然大环化对效力的影响各不相同,但对选择性产生深远影响是常见的。大环化还可以为膜通透性、外排率、血脑屏障穿透性和代谢稳定性带来益处。这些发现促使我们提出一些特定情况,即针对激酶或其他传统上易于成药的靶点类别的药物研发人员应考虑采用大环化合物方法。