Laboratory for Medicinal Chemistry Research, Shionogi Pharmaceutical Research Center, 1-1 Futaba-cho 3-chome, Toyonaka, Osaka 561-0825, Japan.
Laboratory for Drug Discovery & Disease Research, Shionogi Pharmaceutical Research Center, 1-1 Futaba-cho 3-chome, Toyonaka, Osaka 561-0825, Japan.
J Med Chem. 2024 Aug 22;67(16):14478-14492. doi: 10.1021/acs.jmedchem.4c01244. Epub 2024 Aug 13.
Psychosis is a distressing symptom commonly occurring in people with dementia. To treat Parkinson's disease psychosis, pimavanserin (), a 5-HT receptor inverse agonist having minimal 5-HT receptor affinity and no dopamine D receptor affinity, was approved in the United States, but not for dementia-related psychosis due to limited efficacy issues. Herein, we report on the identification of a potent and dual 5-HT and 5-HT receptor inverse agonist having minimal hERG inhibition, after having demonstrated the involvement of both 5-HT and 5-HT receptors to deliver antipsychotic efficacy in an MK-801-induced locomotor model and having conducted 5-HT and 5-HT occupancy studies including a surrogate method. The introduction of a spirocyclopropyl group boosting 5-HT affinity in followed by further optimization to control lipophilicity resulted in balanced dual potency and metabolic stability, and mitigating hERG inhibition led to that showed significant antipsychotic efficacy due to the involvement of both receptors.
精神病是痴呆患者常见的一种痛苦症状。为了治疗帕金森病精神病,美国批准了 pimavanserin(),一种 5-HT 受体反向激动剂,对 5-HT 受体亲和力低,对多巴胺 D 受体亲和力低,但由于疗效有限,不适用于与痴呆相关的精神病。在此,我们报告了一种有效的双 5-HT 和 5-HT 受体反向激动剂的鉴定,该激动剂对 hERG 的抑制作用很小,此前我们已经证明 5-HT 和 5-HT 受体都参与了 MK-801 诱导的运动模型中的抗精神病作用,并进行了 5-HT 和 5-HT 占有率研究,包括替代方法。在 中引入螺环丙基基团可提高 5-HT 的亲和力,然后进一步优化以控制脂溶性,从而实现平衡的双重效力和代谢稳定性,并减轻 hERG 抑制作用,导致 涉及到两个受体,表现出显著的抗精神病作用。