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in vitro tyrimų duomenys rodo, kad regorafenibą metabolizuoja citochromas cyp3a4 ir uridindifosfato gliukuronoziltranferazė ugt1a9.
in vitro data indicate that regorafenib is metabolized by cytochrome cyp3a4 and uridine diphosphate glucuronosyl transferase ugt1a9.
Son Güncelleme: 2017-04-26
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regorafenibas yra uridindifosfato gliukuronoziltransferazės (ugt) 1a1 inhibitorius (žr. 4.5 skyrių).
regorafenib is a uridine diphosphate glucuronosyl transferase (ugt) 1a1 inhibitor (see section 4.5).
Son Güncelleme: 2017-04-26
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in vitro duomenys rodo, kad aksitinibo metabolizmą daugiausia veikia cyp3a4/5 ir mažesne apimtimi cyp1a2, cyp2c19 bei uridindifosfato gliukuronoziltransferazė (ugt) 1a1.
in vitro data indicate that axitinib is metabolised primarily by cyp3a4/5 and, to a lesser extent, cyp1a2, cyp2c19, and uridine diphosphate-glucuronosyltransferase (ugt) 1a1.
Son Güncelleme: 2017-04-26
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jeigu per bandymus in vitro arba in vivo, naudojant skirtingų rūšių gyvūnus arba taikant skirtingas sąlygas pastebima toksikologiniu požiūriu svarbių bandomosios cheminės medžiagos metabolinių savybių pokyčių, gali reikėti apibūdinti susijusius fermentus (pvz., i fazės fermentus, pvz., nuo citochromo p450 priklausomos monooksigenazės sistemos izofermentus, ii fazės fermentus, pvz., sulfotransferazės arba uridindifosfato gliukuronoziltransferazės izofermentus, arba kitus susijusius fermentus).
if toxicologically significant alterations in the metabolic profile of the test chemical are observed through either in vitro or in vivo experiments with different species or conditions, characterisation of the enzyme(s) involved may be needed (e.g. phase i enzymes such as isoenzymes of the cytochrome p450-dependent mono-oxygenase system, phase ii enzymes such as isoenzymes of sulfotransferase or uridine diphosphate glucuronosyl transferase, or any other relevant enzymes).
Son Güncelleme: 2014-11-21
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