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pubmed-article:7264907rdf:typepubmed:Citationlld:pubmed
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pubmed-article:7264907pubmed:abstractTextA series of 4-imidazolylmethyl arylsulfides, sulfoxides, and sulfones and two carbon isosteres of 4-imidazolylmethylphenyl sulfide (I) were synthesized and tested for inhibition of histidine decarboxylase from rat stomach. None of these analogs of I met the criterion of a potent and specific inhibitor of histidine decarboxylase.lld:pubmed
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pubmed-article:7264907pubmed:issn0022-3549lld:pubmed
pubmed-article:7264907pubmed:authorpubmed-author:MillerC ACAlld:pubmed
pubmed-article:7264907pubmed:authorpubmed-author:KelleyJ LJLlld:pubmed
pubmed-article:7264907pubmed:authorpubmed-author:McLeanE WEWlld:pubmed
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pubmed-article:7264907pubmed:volume70lld:pubmed
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pubmed-article:7264907pubmed:pagination341-3lld:pubmed
pubmed-article:7264907pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7264907pubmed:articleTitleInhibition of histidine decarboxylase by imidazole derivatives.lld:pubmed
pubmed-article:7264907pubmed:publicationTypeJournal Articlelld:pubmed