| Literature DB >> 34953340 |
Shinji Nakamura1, Masahiro Kamaura1, Yuichiro Akao1, Natsuko Nakamura1, Atsushi Mizukami1, Akihiko Goto1, Naoki Furuyama1, Nobuo Cho1, Shizuo Kasai2.
Abstract
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.Entities:
Keywords: Age-related macular degeneration (AMD); Diabetes; Protein–protein interaction (PPI); Retinol-binding protein 4 (RBP4); Transthyretin (TTR)
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Year: 2021 PMID: 34953340 DOI: 10.1016/j.bmc.2021.116553
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641