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pubmed-article:3411439pubmed:abstractTextThe metabolites of diltiazem in the urine of rats, dogs and man and rat bile were investigated. New metabolites including six acidic metabolites (A1-A6) and four basic metabolites (M9, MB, MC, MD) were isolated by high performance liquid chromatography and their structures were characterized by gas chromatography-mass spectrometry. Acidic metabolites A1, A2, A3, A4 and basic metabolite MD identified by comparing their properties with the synthetic compounds; (+)-(2S, 3S)-2-(4-methoxyphenyl)-3-acetoxy-4-oxo-2,3,4,5-tetrahydro-1,5- benzothiazepin-5-acetic acid (A1), 3-deacetyl-A1 (A2), O-demethyl-A1 (A3), O-demethyl-3-deacetyl-A1 (A4) and N-didemethyl-diltiazem (MD). All acidic metabolites have a CH2COOH group which may be formed by oxidative deamination of the CH2CH2N(CH3)2 group of diltiazem.lld:pubmed
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pubmed-article:3411439pubmed:pagination211-23lld:pubmed
pubmed-article:3411439pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:3411439pubmed:articleTitleMetabolism of diltiazem. I. Structures of new acidic and basic metabolites in rat, dog and man.lld:pubmed
pubmed-article:3411439pubmed:affiliationBiological Research Laboratory, Tanabe Seiyaku Co., Saitama, Japan.lld:pubmed
pubmed-article:3411439pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3411439pubmed:publicationTypeComparative Studylld:pubmed