增食欲素
敌手
体内
药理学
生物
受体拮抗剂
新陈代谢
排泄
受体
内科学
内分泌学
食欲素受体
化学
生物化学
神经肽
医学
生物技术
作者
Alexander Treiber,Stéphane Delahaye,Aude Weigel,Päivi Aeänismaa,John Gatfield,Swen Seeland
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2023-02-21
卷期号:53 (3): 173-183
标识
DOI:10.1080/00498254.2023.2183159
摘要
Daridorexant is a dual orexin receptor antagonist developed for the treatment of insomnia disorder and has shown improvement in sleep outcomes and daytime functioning. The present work describes its biotransformation pathways in vitro and in vivo and provides a cross-species comparison between the animal species used in preclinical safety assessments and man.Daridorexant clearance is driven by metabolism along seven distinct pathways. Metabolic profiles were characterised by downstream products while primary metabolic products were of minor importance. The metabolic pattern differed between rodent species, with the rat reflecting the human pattern better than the mouse.In rodents, daridorexant is mostly excreted via the bile after extensive metabolism while urinary excretion was negligible in the rat. Only traces of the parent drug were detected in urine, bile, or faeces.Daridorexant has three major metabolites which are well covered in these preclinical safety species. All of them retain some residual affinity towards orexin receptors. However, none of these is considered to contribute to the pharmacological effect of daridorexant as their active concentrations in the human brain are too low.
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