Center for Drug Discovery, Research Triangle Institute, Research Triangle Park, Research Triangle Park, North Carolina 27709, United States.
Bowles Center for Alcohol Studies, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
J Med Chem. 2022 Jun 9;65(11):7959-7974. doi: 10.1021/acs.jmedchem.2c00508. Epub 2022 May 20.
The neuropeptide relaxin-3/RXFP3 system is involved in many important physiological processes such as stress responses, appetite control, and motivation for reward. To date, pharmacological studies of RXFP3 have been limited to peptide ligands. In this study, we report the discovery of the first small-molecule antagonists of RXFP3 through a high-throughput screening campaign. Focused structure-activity relationship studies of the hit compound resulted in RLX-33 () that was able to inhibit relaxin-3 activity in a battery of functional assays. RLX-33 is selective for RXFP3 over RXFP1 and RXFP4, two related members in the relaxin/insulin superfamily, and has favorable pharmacokinetic properties for behavioral assessment. When administered to rats intraperitoneally, RLX-33 blocked food intake induced by the RXFP3-selective agonist R3/I5. Collectively, our findings demonstrated that RLX-33 represents a promising antagonist scaffold for the development of drugs targeting the relaxin-3/RXFP3 system.
神经肽松弛素-3/RXFP3 系统参与许多重要的生理过程,如应激反应、食欲控制和奖励动机。迄今为止,RXFP3 的药理学研究仅限于肽配体。在这项研究中,我们通过高通量筛选发现了第一个 RXFP3 的小分子拮抗剂。对命中化合物进行的重点构效关系研究导致了 RLX-33(),它能够在一系列功能测定中抑制松弛素-3 的活性。RLX-33 对 RXFP3 具有选择性,而对相关的松弛素/胰岛素超家族成员 RXFP1 和 RXFP4 没有选择性,并且具有用于行为评估的良好药代动力学特性。当腹腔内给予大鼠 RLX-33 时,它可以阻断 RXFP3 选择性激动剂 R3/I5 引起的摄食。总的来说,我们的发现表明 RLX-33 代表了一种有前途的拮抗剂支架,可用于开发针对松弛素-3/RXFP3 系统的药物。