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pubmed-article:11844695pubmed:abstractTextA series of alkylidene hydrazide derivatives containing an alkoxyaryl moiety was optimized. The resulting hydrazide-ethers were competitive antagonists at the human glucagon receptor. Pharmacokinetic experiments showed fast clearance of most of the compounds tested. A representative compound [4-hydroxy-3-cyanobenzoic acid (4-isopropylbenzyloxy-3,5-dimethoxymethylene)hydrazide] with an IC50 value of 20 nM was shown to reduce blood glucose levels in fasted rats.lld:pubmed
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pubmed-article:11844695pubmed:articleTitleHuman glucagon receptor antagonists based on alkylidene hydrazides.lld:pubmed
pubmed-article:11844695pubmed:affiliationPfizer Global Research and Development, 10770 Science Center Dr., San Diego, CA 92121, USA. anthony.ling@agouron.comlld:pubmed
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