化学
视黄醇结合蛋白
视黄醇
维加维斯
生物化学
计算生物学
维生素
医学
生物
内分泌学
脂肪因子
胰岛素抵抗
胰岛素
作者
Shinji Nakamura,Masahiro Kamaura,Yuichiro Akao,Natsuko Nakamura,Atsushi Mizukami,Akihiko Goto,Naoki Furuyama,Nobuo Cho,Shizuo Kasai
标识
DOI:10.1016/j.bmc.2021.116553
摘要
Retinol-binding protein 4 (RBP4) is a potential drug target for metabolic and ophthalmologic diseases. A high-throughput screening of our compound library has identified a small-molecule RBP4 reducer 7a, as a hit compound. Aiming to provide a suitable tool for investigating the pharmacological effects of RBP4 reducers, we conducted a structure-activity relationship study of 7a. Exploration of the aryl head, oxazole core, and propanoic acid tail of 7a resulted in the discovery of novel, potent, and orally available phenylpyrrolidine derivatives 43b and 43c. Compound 43b had a potent and long-lasting blood RBP4-level-reducing effect when orally administered to mice at a dose as low as 0.3 mg/kg.
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