m+Medelevator.RU
← Поиск публикаций
Journal of medicinal chemistry · 2026

Discovery of Potent and Brain-Penetrant Inverse Agonists for GPR61, an Orphan G Protein-Coupled Receptor.

СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Fisher Ethan L, Dechert Schmitt Anne-Marie, Tuttle Jamison B, Unwalla Ray, Lovett Gabrielle H, Kormos Bethany L, Coffman Karen J, Zhou Dahui, Moran Michael, Williams Jade, Xiao Jun, LaChapelle Erik A, Fortin Jean-Philippe, Sheikh Abdul Q, Stevens Kimberly A, Kong Jimmy X, Hughes Emily A G, Esquejo Ryan M, Joaquim Stephanie, Amar Nalissa L, Archambault Danielle, Garren Jeonifer, Breen Danna, Jagarlapudi Srinath, Dullea Robert, O'Connor Rebecca E, Koslov-Davino Erika, Callegari Ernesto, Dias João M, Lees Joshua A, Borzilleri Kris, Han Seungil, Brooks Jonathan, Vajdos Felix F, Goyal Ashish, Zhang Lei, Zhang Yuan

Аннотация

GPR61 is a class A orphan G protein-coupled receptor (GPCR) that is predominantly expressed in the pituitary gland and appetite-regulating centers of the brain. Genome-wide association analysis, epigenetic analysis, and animal model data have suggested that GPR61 could be a potential therapeutic target for appetite and body weight modulation. Herein, we describe our medicinal chemistry efforts in discovering a class of potent, selective, and brain-penetrant GPR61 inverse agonists. The cryogenic electron microscopy structure of GPR61 bound to compound 15 shows that this class of inverse agonists binds to an induced, intracellular, allosteric pocket and abolishes GPR61 constitutive activity by disrupting its interactions with G protein, representing a novel mode of action of GPCR inverse agonism.

Предметные рубрики MeSH