Details of the Metabolic Reaction (MR)

General Information of This Metabolic Reaction (MR) (ID: MR008880)
Formula
CYP3A4 ...
SVG example
Ketone formation
Reactant Ruxolitinib M16 metabolite Product Ruxolitinib M9 metabolite
Reactant Info Product Info
Metabolic Enzyme Cytochrome P450 3A4 (CYP3A4) DME Info
Cytochrome P450 2C9 (CYP2C9) DME Info
Metabolic Type Other reaction - Ketone formation
Other MR(s) Related to The Reactant of This MR
Other MR(s) That Produce The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR002027 Phenprocoumon 8-hydroxy-R-phenprocoumon Oxidation - 8-Hydroxylation Phenprocoumon [1]
MR008879 Ruxolitinib Ruxolitinib M16 metabolite Oxidation - 3-hydroxylation Ruxolitinib [2], [3]
MR002215 Ruxolitinib phosphate Ruxolitinib M16 metabolite Oxidation - 3-Hydroxylation Ruxolitinib phosphate [2]
References
1 Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development. Curr Med Chem. 2009;16(27):3480-675.
2 Metabolism, excretion, and pharmacokinetics of [14C]INCB018424, a selective Janus tyrosine kinase 1/2 inhibitor, in humans Drug Metab Dispos. 2010 Nov;38(11):2023-31. doi: 10.1124/dmd.110.033787.
3 The effect of CYP3A4 inhibition or induction on the pharmacokinetics and pharmacodynamics of orally administered ruxolitinib (INCB018424 phosphate) in healthy volunteers

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