- The discovery of potent antagonists of NPBWR1 (GPR7).
The discovery of potent antagonists of NPBWR1 (GPR7).
Bioorganic & medicinal chemistry letters (2011-12-27)
F Anthony Romero, Nicholas B Hastings, Remond Moningka, Zhiqiang Guo, Ming Wang, Jerry Di Salvo, Ying Lei, Dorina Trusca, Qiaolin Deng, Vincent Tong, Jenna L Terebetski, Richard G Ball, Feroze Ujjainwalla
PMID22197390
RESUMO
The synthesis and evaluation of small molecule antagonists of the G protein-coupled receptor NPBWR1 (GPR7) are reported for the first time. [4-(5-Chloropyridin-2-yl)piperazin-1-yl][(1S,2S,4R)-4-{[(1R)-1-(4-methoxyphenyl)ethyl]amino}-2-(thiophen-3-yl)cyclohexyl]methanone (1) emerged as a hit from a high-throughput screen. Examination of substituents that focused on replacing the 5-chloropyridine and 4-methoxybenzylamino groups of 1 led to the identification of compounds that exhibited subnanomolar potencies as low as 660pM (9k) in the functional assay and 200pM in the binding assay (9i).