化学
多巴胺受体D3
部分
对映体
兴奋剂
G蛋白偶联受体
立体化学
对接(动物)
选择性
分子模型
结合选择性
部分激动剂
受体
配体(生物化学)
组合化学
多巴胺受体
生物化学
医学
护理部
催化作用
作者
Liang Tan,Qingtong Zhou,Wenzhong Yan,Jian Sun,Alan P. Kozikowski,Suwen Zhao,Xi‐Ping Huang,Jianjun Cheng
标识
DOI:10.1021/acs.jmedchem.9b01835
摘要
2-Phenylcyclopropylmethylamine (PCPMA) analogues have been reported as selective serotonin 2C agonists. On the basis of the same scaffold, we designed and synthesized a series of bitopic derivatives as dopamine D3R ligands. A number of these new compounds show a high binding affinity for D3R with excellent selectivity. Compound (1R,2R)-22e and its enantiomer (1S,2S)-22e show a comparable binding affinity for the D3R, but the former is a potent D3R agonist, while the latter acts as an antagonist. Molecular docking studies revealed different binding poses of the PCPMA moiety within the orthosteric binding pocket of the D3R, which might explain the different functional profiles of the enantiomers. Compound (1R,2R)-30q shows a high binding affinity for the D3R (Ki = 2.2 nM) along with good selectivity, as well as good bioavailability and brain penetration properties in mice. These results reveal that the PCPMA scaffold may serve as a privileged scaffold for the design of aminergic GPCR ligands.
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