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Journal of Medicinal Chemistry|March 1, 1991
Renin inhibitors containing conformationally restricted P1-P1' dipeptide mimeticsP D Williams, D S Perlow, L S Payne, et al.Bioorganic & Medicinal Chemistry Letters|August 11, 2000
Selective alpha1a adrenergic receptor antagonists based on 4-aryl-3,4-dihydropyridine-2-onesP G Nantermet, J C Barrow, H G Selnick, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Discovery and initial structure-activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonistsJ C Barrow, P G Nantermet, H G Selnick, et al.Journal of Medicinal Chemistry|June 17, 1998
Development of orally active oxytocin antagonists: studies on 1-(1-[4-[1-(2-methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl]piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and related pyridinesI M Bell, J M Erb, R M Freidinger, et al.Journal of Medicinal Chemistry|November 26, 1997
Discovery of a novel, selective, and orally bioavailable class of thrombin inhibitors incorporating aminopyridyl moieties at the P1 positionD M Feng, S J Gardell, S D Lewis, et al.Journal of Medicinal Chemistry|July 14, 2000
In vitro and in vivo evaluation of dihydropyrimidinone C-5 amides as potent and selective alpha(1A) receptor antagonists for the treatment of benign prostatic hyperplasiaJ C Barrow, P G Nantermet, H G Selnick, et al.Proceedings of the National Academy of Sciences of the United States of America|September 2, 1998
Synthesis and biological activities of potent peptidomimetics selective for somatostatin receptor subtype 2L Yang, S C Berk, S P Rohrer, et al.Pageof 5