Huang Boshi, Ma Hongguang, Pagare Piyusha P, Li Mengchu, Mendez Rolando E, Gillespie James C, Poklis Justin L, Halquist Matthew S, Stevens David L, Dewey William L, Selley Dana E, Zhang Yan
Department of Medicinal Chemistry, School of Pharmacy, Virginia Commonwealth University, 800 E Leigh Street, Richmond, Virginia23298, United States.
Department of Pharmacology and Toxicology, School of Medicine, Virginia Commonwealth University, 410 North 12th Street, Richmond, Virginia23298, United States.
ACS Pharmacol Transl Sci. 2024 Dec 5;7(12):4165-4182. doi: 10.1021/acsptsci.4c00593. eCollection 2024 Dec 13.
The development of highly potent and selective μ opioid receptor (MOR) modulators with favorable drug-like properties has always been a focus in the opioid domain. Our previous efforts led to the discovery of a lead compound designated as NAT, a potent centrally acting MOR modulator. However, the fact that NAT precipitated considerable withdrawal effects at higher doses largely impaired its further development. In the light of the concept of activity cliff and CNS multiparameter optimization algorithm, a nitrogen atom was incorporated into the thiophene ring of NAT, aiming to preserve desirable pharmacological activities and CNS permeability while alleviating withdrawal symptoms. Among all 16 new analogs, compound (NTZ) exhibited improved opioid receptor selectivity, enhanced antagonistic effect, and overall fewer withdrawal symptoms compared to NAT. Further assessment of several key drug-like properties suggested a favorable ADMET profile of NTZ. Taken together, NTZ shows promise as a potential lead to treat opioid use disorder.
开发具有良好类药物性质的高效且选择性的μ阿片受体(MOR)调节剂一直是阿片类药物领域的一个重点。我们之前的努力导致发现了一种先导化合物,命名为NAT,一种强效的中枢作用MOR调节剂。然而,NAT在较高剂量下会引发相当程度的戒断效应,这一事实在很大程度上阻碍了其进一步开发。根据活性悬崖概念和中枢神经系统多参数优化算法,在NAT的噻吩环中引入了一个氮原子,旨在保留理想的药理活性和中枢神经系统通透性,同时减轻戒断症状。在所有16种新类似物中,化合物(NTZ)与NAT相比,表现出改善的阿片受体选择性、增强的拮抗作用以及总体上更少的戒断症状。对几个关键类药物性质的进一步评估表明NTZ具有良好的药代动力学、吸收、分布、代谢和排泄(ADMET)特性。综上所述,NTZ有望成为治疗阿片类药物使用障碍的潜在先导药物。