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Advances in Experimental Medicine and Biology|January 1, 1995
Progress in the development of oxytocin antagonists for use in preterm laborD J Pettibone, M Guidotti, C M Harrell, et al.The Journal of Pharmacology and Experimental Therapeutics|January 1, 1993
Identification of an orally active, nonpeptidyl oxytocin antagonistD J Pettibone, B V Clineschmidt, M T Kishel, et al.The Journal of Pharmacology and Experimental Therapeutics|December 1, 1995
Pharmacology of L-754,142, a highly potent, orally active, nonpeptidyl endothelin antagonistD L Williams, K L Murphy, N A Nolan, et al.Bioorganic & Medicinal Chemistry|September 1, 1994
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformationP D Williams, R G Ball, B V Clineschmidt, et al.The Journal of Pharmacology and Experimental Therapeutics|January 1, 1991
In vitro pharmacological profile of a novel structural class of oxytocin antagonistsD J Pettibone, B V Clineschmidt, E V Lis, et al.Journal of Medicinal Chemistry|October 16, 1992
Orally active, nonpeptide oxytocin antagonistsB E Evans, J L Leighton, K E Rittle, et al.European Journal of Pharmacology|April 24, 1991
Bradykinin agonist activity of a novel, potent oxytocin antagonistD J Pettibone, B V Clineschmidt, E V Lis, et al.Endocrinology|July 1, 1989
A structurally unique, potent, and selective oxytocin antagonist derived from Streptomyces silvensisD J Pettibone, B V Clineschmidt, P S Anderson, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Nonpeptide oxytocin antagonists: potent, orally bioavailable analogs of L-371,257 containing a 1-R-(pyridyl)ethyl ether terminusM S Kuo, M G Bock, R M Freidinger, 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.Pageof 6