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Molecular Pharmacology|June 1, 1989
Characterization of the binding of [3H]L-365,260: a new potent and selective brain cholecystokinin (CCK-B) and gastrin receptor antagonist radioligandR S Chang, T B Chen, M G Bock, et al.Journal of Medicinal Chemistry|September 1, 1978
Synthesis and analgesic activity of 1,3-dihydro-3-(substituted phenyl)imidazo[4,5-b]pyridin-2-ones and 3-(substituted phenyl)-1,2,3-triazolo[4,5-b]pyridinesR L Clark, A A Pessolano, T Y Shen, et al.The Journal of Pharmacology and Experimental Therapeutics|May 1, 1985
Selectivity of (+)-4-propyl-9-hydroxynaphthoxazine [(+)-PHNO] for dopamine receptors in vitro and in vivoG E Martin, M Williams, D J Pettibone, et al.Journal of Medicinal Chemistry|August 1, 1989
Cholecystokinin antagonists. Synthesis and biological evaluation of 3-substituted benzolactamsW H Parsons, A A Patchett, M K Holloway, et al.American Journal of Hypertension|September 1, 1992
AT1 receptors mediate the release of prostaglandins in porcine smooth muscle cells and rat astrocytesK H Leung, R S Chang, V J Lotti, et al.Journal of Medicinal Chemistry|September 1, 1984
Adrenoceptor and tetrabenazine antagonism activities of some pyridinyltetrahydropyridinesW S Saari, W Halczenko, J R Huff, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1986
L-654,284 a new potent and selective alpha 2-adrenoceptor antagonistD J Pettibone, B V Clineschmidt, V J Lotti, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|August 1, 1987
Pharmacological profile of a new potent and specific alpha 2-adrenoceptor antagonist, L-657,743D J Pettibone, B V Clineschmidt, V J Lotti, et al.The Journal of Pharmacology and Experimental Therapeutics|July 1, 1992
In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonistR S Chang, P K Siegl, B V Clineschmidt, et al.Journal of Medicinal Chemistry|January 1, 1988
Cholecystokinin antagonists. Synthesis and biological evaluation of 4-substituted 4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepinesM G Bock, R M DiPardo, B E Evans, et al.Pageof 8