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ritonavir kan inducere glucuronidering af methadon.
ritonavir may induce glucuronidation of methadone.

den største udskillelsesvej i katte er glucuronidering.
the major elimination pathway in cats is glucuronidation.

raltegravir elimineres primært ved glucuronidering i leveren.
raltegravir is eliminated primarily by glucuronidation in the liver.

leverinsufficiens ralteravir elimineres primært ved glucuronidering i leveren.
12 hepatic impairment raltegravir is eliminated primarily by glucuronidation in the liver.

irbesartan metaboliseres hovedsageligt af cyp2c9 og i mindre udstrækning ved glucuronidering.
irbesartan is mainly metabolised by cyp2c9 and to a lesser extent by glucuronidation.

irbesartan er metaboliseres hovedsageligt af cyp2c9 og i mindre udstrækning ved glucuronidering.
irbesartan is mainly metabolised by cyp2c9 and to a lesser extent by glucuronidation.

ritonavir inducerer glucuronidering og som følge heraf forventes fald i atovaquons plasmakoncentration.
interaction with indinavir/ ritonavir not studied ritonavir induces glucuronidation and as a result is expected to decrease the plasma concentrations of atovaquone.

n-methylering, n-glucuronidering og oxidering i imidazolringen er også observeret.
n-methylation, n-glucuronidation and oxidation in the imidazole ring have also been observed.

de sekundære biotransformationveje, der involverer de primære biotransformationsprodukter, omfatter glucuronidering og dehydrogenering.
secondary biotransformation pathways involving the primary biotransformation products included glucuronidation and dehydrogenation.

i overensstemmelse med resultaterne af in vitro forsøg hæmmes atorvastatins metabolisering via glucuronidering af gemfibrozil.
according to results of in vitro studies the metabolic pathway of atorvastatin via glucuronidation is inhibited by gemfibrozil.

4 etravirin metaboliseres af cyp3a4, cyp2c9 og cyp2c19 efterfulgt af glucuronidering via uridindifosfatglucuronosyltransferase (udpgt).
medicinal products that affect etravirine exposure etravirine is metabolised by cyp3a4, cyp2c9 and cyp2c19 followed by glucuronidation by uridine diphosphate glucuronosyl transferase (udpgt).

data indikerer således, at raltegravirs væsentligste clearance-mekanisme hos mennesker er ugt1a1-medieret glucuronidering.
thus the data indicate that the major mechanism of clearance of raltegravir in humans is ugt1a1-mediated glucuronidation.

mirabegron metaboliseres via flere pathways, som involverer dealkylering, oxidation, (direkte) glucuronidering og amidhydrolyse.
mirabegron is metabolized via multiple pathways involving dealkylation, oxidation, (direct) glucuronidation, and amide hydrolysis.

baseret på in vitro - og in vivo- undersøgelser elimineres raltegravir hovedsageligt ved metabolisme via ugt1a1- medieret glucuronidering.
based on in vitro and in vivo studies, raltegravir is eliminated mainly by metabolism via a ugt1a1-mediated glucuronidation pathway.

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).

glucuronideringen resulterede i dannelsen af telmisartans 1-o-acylglucuronidmetabolit.
the glucuronidation resulted in the formation of the 1-o-acylglucuronide metabolite of telmisartan.