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dc.contributor.authorYoo, Hye Hyun-
dc.contributor.authorSon, Junghyun-
dc.contributor.authorLee, Jaeick-
dc.contributor.authorKim, Nam Sun-
dc.contributor.authorShin, Myungyoup-
dc.contributor.authorKang, Min-Jung-
dc.contributor.authorKim, Dong-Hyun-
dc.date.accessioned2024-01-21T03:00:24Z-
dc.date.available2024-01-21T03:00:24Z-
dc.date.created2021-09-02-
dc.date.issued2006-07-
dc.identifier.issn0951-4198-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/135356-
dc.description.abstractThe metabolism and excretion of 2-methylaminoethoxycarbonyl-4,4'-dimethoxy-5,6,5',6'-dimethylenedioxybiphenyl-2"-carboxylic acid (DDB-S) were investigated in both rats and humans using liquid chromatography/electrospray ion trap mass spectrometry (LC/ESI-MS/MS). In rats, DDB-S was rapidly eliminated from the body after a single 50mg/kg intravenous injection, with urine being a major excretion route. DDB-S was metabolically stable; approximately 96% of the administered dose was recovered in the form of the parent compound. Nevertheless, 12 metabolites were detected in the urine and feces collected from DDB-S-treated rats. The structural characterizations of the metabolites were elucidated from the MSn spectral analysis. Because DDB-S has a pseudo-symmetrical methylenedioxy biphenyl structure, regioselective deuterium-substituted DDB-S (d(5)-DDB-S) was used to assign the metabolic modification. The major metabolic pathways of DDB-S were identified as demethylenation of the methylenedioxy moiety, O-demethylation of the methoxy moiety and glucuronidation. In addition, N-demethylation of the methylaminoethyl group was also detected as a minor reaction. Copyright (c) 2006 John Wiley & Sons, Ltd.-
dc.languageEnglish-
dc.publisherWILEY-
dc.subjectHUMAN LIVER-MICROSOMES-
dc.subjectASYMMETRIC HYDROGENATION-
dc.subjectMECHANISM-
dc.subjectDIMETHYL-4,4&apos-
dc.subject-DIMETHOXY-5,6,5&apos-
dc.subject,6&apos-
dc.subject-DIMETHYLENEDIOXYBIPHENYL-2,2&apos-
dc.subject-DICARBOX YLATE-
dc.subjectINJURY-
dc.titleThe metabolism and excretion of 2-methylaminoethoxycarbonyl-4,4 '-dimethoxy-5,6,5,6 '-dimethylenedioxybiphenyl-2 '-carboxylic acid (DDB-S) in rats and human-
dc.typeArticle-
dc.identifier.doi10.1002/rcm.2549-
dc.description.journalClass1-
dc.identifier.bibliographicCitationRAPID COMMUNICATIONS IN MASS SPECTROMETRY, v.20, no.13, pp.1981 - 1988-
dc.citation.titleRAPID COMMUNICATIONS IN MASS SPECTROMETRY-
dc.citation.volume20-
dc.citation.number13-
dc.citation.startPage1981-
dc.citation.endPage1988-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000238903600003-
dc.identifier.scopusid2-s2.0-33745791362-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategorySpectroscopy-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaSpectroscopy-
dc.type.docTypeArticle-
dc.subject.keywordPlusHUMAN LIVER-MICROSOMES-
dc.subject.keywordPlusASYMMETRIC HYDROGENATION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusDIMETHYL-4,4&apos-
dc.subject.keywordPlus-DIMETHOXY-5,6,5&apos-
dc.subject.keywordPlus,6&apos-
dc.subject.keywordPlus-DIMETHYLENEDIOXYBIPHENYL-2,2&apos-
dc.subject.keywordPlus-DICARBOX YLATE-
dc.subject.keywordPlusINJURY-
dc.subject.keywordAuthorDDB-S-
dc.subject.keywordAuthormetabolism-
dc.subject.keywordAuthorregioselectivity-
dc.subject.keywordAuthorP450-
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