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biotransformationen finder hovedsageligt sted ved oxidativ nedbrydning af morfolindelen og hydrolyse af amidbindingerne.
oxidative degradation of the morpholinone moiety and hydrolysis of the amide bonds are the major sites of biotransformation.
oxidativ nedbrydning af fedtstoffer foregår via dannelsen af frie radikaler, som elimineres af antioxidanter.
oxidative attacks on lipids proceed through the mediation of free radicals which are eliminated by antioxidants.
in vitro studier viste ingen signifikant involvering af oxidativ metabolisering med cytochrom p450 enzymer.
in vitro studies did not show any significant involvement of oxidative metabolism by cytochrome p450 enzymes.
glimepirid metaboliseres fuldstændig ved hjælp af oxidativ biotransformation både efter intravenøs indgivelse og efter peroral indtagelse.
glimepiride is completely metabolised by oxidative biotransformation after either an intravenous or oral dose.
eksperimenter in vitro indikerer, at rilpivirinhydrochlorid primært undergår oxidativ metabolisme medieret af cyp3a-systemet.
in vitro experiments indicate that rilpivirine hydrochloride primarily undergoes oxidative metabolism mediated by the cyp3a system.
elvitegravir gennemgår primært oxidativ metabolisme via cyp3a og glukuronideres i mindre grad via ugt1a1/3-enzymer.
elvitegravir undergoes primarily oxidative metabolism via cyp3a, and is secondarily glucuronidated via ugt1a1/3 enzymes.
asenapin udskilles primært ved direkte glucuronidering af ugt1a4 og oxidativ metabolisme ved cytochrom p450-isoenzymer (overvejende cyp1a2).
asenapine is cleared primarily through direct glucuronidation by ugt1a4 and oxidative metabolism by cytochrome p450 isoenzymes (predominantly cyp1a2).