Publication:
Chemical and metabolic studies on N-benzyl-tert-butylamine and its potential metabolites

dc.contributor.authorsUlgen M., Yilmaz F., Unsalan S., Gorrod J.W.
dc.date.accessioned2022-03-15T01:53:09Z
dc.date.accessioned2026-01-11T14:27:43Z
dc.date.available2022-03-15T01:53:09Z
dc.date.issued1995
dc.description.abstractThe metabolism of N-benzyl-tert-butylamine was studied in vitro using male hamster hepatic microsomal preparations. This substrate produced the corresponding nitrone, benzaldehyde and an uncharacterised metabolite. No metabolites were detected which corresponded to either authentic amide or oxaziridine. The results indicate that the nitrone observed as a metabolite in this experiment is not an intermediate leading to the formation of an oxaziridine and hence an amide, under careful experimental conditions excluding light. © Freund Publishing House, Ltd. 1995
dc.identifier.doi10.1515/DMDI.1995.12.2.131
dc.identifier.issn7925077
dc.identifier.pubmed8591691
dc.identifier.urihttps://hdl.handle.net/11424/246276
dc.language.isoeng
dc.relation.ispartofDrug Metabolism and Drug Interactions
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjecthamster
dc.subjectmetabolism
dc.subjectmicrosomes
dc.subjectN-benzyl-tert-butylamine
dc.subjectnitrones
dc.subjectoxaziridines
dc.titleChemical and metabolic studies on N-benzyl-tert-butylamine and its potential metabolites
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage144
oaire.citation.issue2
oaire.citation.startPage131
oaire.citation.titleDrug Metabolism and Drug Interactions
oaire.citation.volume12

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