Department of Chemistry, Faculty of Science, Sultan Qaboos University, PO Box 36, Postal Code 123, Muscat, Oman.
Pharma-Center Bonn, Pharmaceutical Institute, Pharmaceutical Chemistry I, An der Immenburg 4, D-53121 Bonn, Germany.
Drug Discov Today. 2019 Jan;24(1):325-333. doi: 10.1016/j.drudis.2018.09.021. Epub 2018 Oct 3.
The P2Y receptor is one of eight known P2Y receptor subtypes, and belongs to the G-protein-coupled receptor (GPCR) family. The P2Y receptor is highly expressed on blood platelets and in the brain. Potent, selective, peripherally acting antagonists for the P2Y receptor are used clinically as antithrombotic drugs. Several different scaffolds have been identified as P2Y receptor antagonists, including irreversibly acting thienotetrahydropyridines (prodrugs), and reversible competitive antagonists, including adenine nucleotide analogs, piperazinyl-glutamate-quinolines, -pyridines, and -pyrimidines, and anthraquinone derivatives. Here, we provide an overview of the different scaffolds that have been developed as P2Y receptor antagonists, some of which have become important therapeutics.
P2Y 受体是已知的 8 种 P2Y 受体亚型之一,属于 G 蛋白偶联受体 (GPCR) 家族。P2Y 受体在血小板和大脑中高度表达。强效、选择性、外周作用的 P2Y 受体拮抗剂临床上用作抗血栓药物。已经确定了几种不同的支架作为 P2Y 受体拮抗剂,包括不可逆作用的噻吩并四氢吡啶(前药)和可逆竞争性拮抗剂,包括腺嘌呤核苷酸类似物、哌嗪基谷氨酸喹啉、-吡啶和-嘧啶以及蒽醌衍生物。在这里,我们概述了已开发为 P2Y 受体拮抗剂的不同支架,其中一些已成为重要的治疗药物。