Novel Potent and Selective Agonists of the GPR55 Receptor Based on the 3-Benzylquinolin-2(1<i>H</i>)-One Scaffold.

导出 OA

翻译打印收藏纠错

作者： Costanza,Ceni ^[1] ; Michael J,Benko ^[2] ; Kawthar A,Mohamed ^[3] ; Giulio,Poli ^[3] ; Miriana,Di Stefano ^[1] ; Tiziano,Tuccinardi ^[1] ; Maria,Digiacomo ^[2] ; Massimo,Valoti ^[1] ; Robert B,Laprairie ^[1] ; Marco,Macchia ^[4] ; Simone,Bertini ^[3]

作者单位： Department of Pharmacy, University of Pisa, Via Bonanno Pisano 6, 56126 Pisa, Italy. ^[1] Doctoral School in Life Sciences, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy. ^[2] College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada. ^[3] Department of Life Sciences, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy. ^[4]

关键词 GPR55 GPR55 agonist GPR55 modulator benzylquinolin-2-one p-ERK activation assay quinolin-2-one

DOI 10.3390/ph15070768

PMID 35890067

发布时间 2022-07-31

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交