Zhang Yue-Mei, Greco Michael, Le Blanc Tonya, Lang Wensheng, Kauffman Jack, Masucci John, Murray William V, Demarest Keith, Macielag Mark Joseph
Janssen Research & Development, 1400 McKean Road, Spring House, Pennsylvania 19477-0776, United States.
ACS Med Chem Lett. 2020 Nov 3;11(12):2504-2509. doi: 10.1021/acsmedchemlett.0c00495. eCollection 2020 Dec 10.
The 6-benzhydryl-4-amino-quinolin-2-ones are peripherally restricted CB receptor inverse agonists (CBRIAs) that have been reported to attenuate obesity and improve insulin sensitivity in the diet-induced obese (DIO) mouse model. However, chronic dosing of select compounds from the series showed time-dependent brain accumulation despite a low brain/plasma exposure ratio. To address this issue, a PEGylation approach was employed to identify a novel series of homodimeric 6-benzhydryl-4-amino-quinazoline-PEG conjugates with an extended half-life. The lead compound engaged peripheral CBRs in a gastrointestinal (GI) tract motility study and demonstrated a high level of peripheral restriction in a chronic DIO mouse pharmacokinetic study.
6-二苯甲基-4-氨基喹啉-2-酮是外周限制型CB受体反向激动剂(CBRIAs),据报道,在饮食诱导肥胖(DIO)小鼠模型中,它们能减轻肥胖并改善胰岛素敏感性。然而,尽管该系列中某些化合物的脑/血浆暴露率较低,但长期给药显示出时间依赖性的脑内蓄积。为解决这一问题,采用聚乙二醇化方法来鉴定一系列具有延长半衰期的新型同二聚体6-二苯甲基-4-氨基喹唑啉-PEG缀合物。在一项胃肠道(GI)道运动性研究中,先导化合物作用于外周CBRs,并在一项慢性DIO小鼠药代动力学研究中表现出高度的外周限制。