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20 angezeigte Treffer · Seite 2, keine Gesamtzahl für „Uridine“
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Febuxostat Krka · 4.5 · Febuxostat metabolism depends on Uridine Glucuronosyl Transferase (UGT) enzymes. Medicinal products that inhib
Eintrag öffnenFebuxostat Viatris (previously Febuxostat Mylan) · 4.5 · Febuxostat metabolism depends on Uridine Glucuronosyl Transferase (UGT) enzymes. Medicinal products that inhib
Eintrag öffnenFebuxostat Viatris (previously Febuxostat Mylan) · 4.5 · Febuxostat metabolism depends on Uridine Glucuronosyl Transferase (UGT) enzymes. Medicinal products that inhib
Eintrag öffnenFloxuridin
Eintrag öffnenFluordesoxyuridylat
Eintrag öffnenGazyvaro · 4.5 · Obinutuzumab is not a substrate, inhibitor, or inducer of cytochrome P450 (CYP450), uridine diphosphate glucur
Eintrag öffnenGlyxambi · 4.5 · Empagliflozin is mainly excreted unchanged. A minor fraction is metabolised via uridine 5'-diphosphoglucuronos
Eintrag öffnenHämolytische Anämie durch Pyrimidin-5'-Nukleotidase-Mangel
Eintrag öffnenIdoxuridin
Eintrag öffnenInaqovi · 4.5 · Cedazuridine is an inhibitor of CDA and thereby increases the exposure of decitabine following oral administra
Eintrag öffnenInaqovi · 4.5 · Decitabine and cedazuridine are not substrates or inhibitors for cytochrome P450 (CYP450); thus interactions w
Eintrag öffnenJuluca · 4.5 · Dolutegravir is eliminated mainly through metabolism by uridine diphosphate glucuronosyl transferase (UGT)1A1.
Eintrag öffnenLonsurf · 4.5 · In vitro studies indicated that trifluridine is a substrate for the nucleoside transporters CNT1, ENT1 and ENT
Eintrag öffnenLonsurf · 4.5 · In vitro studies indicated that trifluridine, tipiracil hydrochloride and 5-[trifluoromethyl] uracil (FTY) did
Eintrag öffnenLorviqua · 4.5 · In vitro data indicate that lorlatinib is primarily metabolised by CYP3A4 and uridine diphosphate-glucuronosyl
Eintrag öffnenMaviret · 4.5 · Glecaprevir and pibrentasvir are weak inhibitors of cytochrome P450 (CYP) 3A and uridine glucuronosyltransfera
Eintrag öffnenMaviret · 4.5 · Glecaprevir and pibrentasvir are weak inhibitors of cytochrome P450 (CYP) 3A and uridine glucuronosyltransfera
Eintrag öffnenOdefsey · 4.5 · Tenofovir alafenamide is not an inhibitor of human uridine diphosphate glucuronosyltransferase (UGT) 1A1 in vi
Eintrag öffnenPseudouridin
Eintrag öffnenSegluromet · 4.5 · Multiple-dose administration of rifampicin (a uridine 5’-diphospho-glucuronosyltransferase [UGT] and cytochrom
Eintrag öffnen