Publication:
In vitro microsomal metabolism of nuclear chloro substituted secondary amines and imines

dc.contributor.authorsKůçükgüzel I., Ülgen M., Gorrod J.W.
dc.date.accessioned2022-03-15T01:53:22Z
dc.date.accessioned2026-01-10T18:39:20Z
dc.date.available2022-03-15T01:53:22Z
dc.date.issued1997
dc.description.abstractThe metabolism of N-(4-chlorobenzyl)-4-chloroaniline (CBCA), N-(4-chlorobenzyl)-4-chlorobenzylamine (CBCBA), and N-(4-chlorobenzylidene)-4-chlorobenzylamine (CBDCBA) were studied in vitro using rat liver microsomal preparations. The secondary amines produced the corresponding N-oxidation products (hydroxylamines and nitrones) and dealkylation products (4-chlorobenzaldehyde and primary amines). Both secondary amines failed to produce the corresponding amides, whilst the parent imine was detected as a metabonate. CBDCBA, the intermediate imine of CBCBA metabolism, was also incubated under similar conditions. However, no oxaziridine was detected.
dc.identifier.doi10.1007/BF03190970
dc.identifier.issn3787966
dc.identifier.urihttps://hdl.handle.net/11424/246318
dc.language.isoeng
dc.publisherSpringer-Verlag France
dc.relation.ispartofEuropean Journal of Drug Metabolism and Pharmacokinetics
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHydroxylamines
dc.subjectMetabolism
dc.subjectNitrones
dc.subjectOxaziridines
dc.subjectSecondary amines
dc.titleIn vitro microsomal metabolism of nuclear chloro substituted secondary amines and imines
dc.typeconferenceObject
dspace.entity.typePublication
oaire.citation.endPage358
oaire.citation.issue4
oaire.citation.startPage351
oaire.citation.titleEuropean Journal of Drug Metabolism and Pharmacokinetics
oaire.citation.volume22

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