Search Results - "Airey, J E"
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Development of high-affinity 5-HT3 receptor antagonists. 1. Initial structure-activity relationship of novel benzamides
Published in Journal of medicinal chemistry (01-03-1992)“…This report describes the development of novel benzamides which are orally active, highly potent, specific antagonists of 5-HT3 receptors. Described in this…”
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Development of high-affinity 5-HT3 receptor antagonists. 2. Two novel tricyclic benzamides
Published in Journal of medicinal chemistry (01-03-1992)“…Two new classes of potent 5-HT3 agents have been developed and examined as inhibitors of cytotoxic drug induced emesis in the ferret and dog. The absolute…”
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RG 12915: a potent 5-hydroxytryptamine-3 antagonist that is an orally effective inhibitor of cytotoxic drug-induced emesis in the ferret and dog
Published in The Journal of pharmacology and experimental therapeutics (01-08-1990)“…RG 12915 [4-[N-(1-azabicyclo[2.2.2.]octan-3-(S)-yl)]2-chloro-cis 5a-(S)-9a-(S)-5a,6,7,8,9,9a-hexahydrobenzofurancarboxamide hydrochloride] is a potent and…”
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Structure and absolute configuration of a high affinity 5-HT3 receptor antagonist, (5aS,9aS)-N-[(3S)-1-azabicyclo[2.2.2]octan-3-yl]-2-chloro- 5a,6,7,8,9,9a-hexahydro-4-dibenzofurancarboxamide hydrochloride
Published in Acta crystallographica. Section C, Crystal structure communications (15-08-1993)“…The absolute configuration was established as (S,S,S) by the R-factor test and by careful measurement of 197 enantiomorph-sensitive Friedel pairs of…”
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Adriamycin analogues. Novel anomeric ribofuranoside analogues of daunorubicin
Published in Journal of medicinal chemistry (01-01-1982)“…The synthesis, cell growth-inhibitory activity, in vivo antileukemic activity, and extent of DNA binding of the alpha- and beta-anomeric…”
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Development of high-affinity 5-HT3 receptor antagonists. II: Two novel tricyclic benzamides
Published in Journal of medicinal chemistry (1992)Get full text
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