作者:Stephen E. de Laszlo、Candice Hacker、Bing Li、Dooseop Kim、Malcolm MacCoss、Nathan Mantlo、James V. Pivnichny、Larry Colwell、Gregory E. Koch、Margaret A. Cascieri、William K. Hagmann
DOI:10.1016/s0960-894x(99)00081-5
日期:1999.3
The SAR of 2-pyridyl-3,5-diaryl pyrroles, ligands of the human glucagon receptor and inhibitors of p38 kinase, were investigated. This effort resulted in the identification of 2-(4-pyridyl)-5-(4-chlorophenyl)-3-(5-bromo-2-propyloxyphenyl)pyrrole 49 (L-168,049), a potent (Kb = 25 nM), selective antagonist of glucagon. (C) 1999 Elsevier Science Ltd. All rights reserved.
Afzal, Obaid; Alamri, Mubarak A.; Altamimi, Abdulmalik S. A., Indian Journal of Heterocyclic Chemistry, 2021, vol. 31, # 4, p. 621 - 634
作者:Afzal, Obaid、Alamri, Mubarak A.、Altamimi, Abdulmalik S. A.、Athar, Fareeda、Bhat, Abdul Roouf、Tuhfa