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British Journal of Pharmacology|May 1, 1995
Functional evidence equating the pharmacologically-defined alpha 1A- and cloned alpha 1C-adrenoceptor: studies in the isolated perfused kidney of ratD R Blue, D W Bonhaus, A P Ford, et al.British Journal of Pharmacology|August 1, 1997
Catecholamine modulatory effects of nepicastat (RS-25560-197), a novel, potent and selective inhibitor of dopamine-beta-hydroxylaseW C Stanley, B Li, D W Bonhaus, et al.Journal of Medicinal Chemistry|September 3, 1993
2-(Quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonistsR D Clark, A B Miller, J Berger, et al.Neuropharmacology|April 1, 1997
RS-102221: a novel high affinity and selective, 5-HT2C receptor antagonistD W Bonhaus, K K Weinhardt, M Taylor, et al.British Journal of Pharmacology|August 24, 1999
RS-127445: a selective, high affinity, orally bioavailable 5-HT2B receptor antagonistD W Bonhaus, L A Flippin, R J Greenhouse, et al.Molecular Pharmacology|February 1, 1996
RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-alpha, alpha-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective alpha 1A-adrenoceptor antagonist, displays low affinity for functional alpha 1-adrenoceptors in human prostate: implications for adrenoceptor classificationA P Ford, N F Arredondo, D R Blue, et al.Pageof 13