General Information of This Metabolic Reaction (MR) (ID: MR013369)
Formula
SVG example
Reactant Methylphenidate Product 6-Oxo-MPH
Reactant Info Product Info
Other MR(s) Related to The Reactant of This MR
Other MR(s) That Metabolize The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR013394 Methylphenidate Alpha-phenyl-2-piperidine acetic acid (ritalinic acid) Hydrolysis - Esterase hydrolyzation Methylphenidate [1], [2]
MR013392 Methylphenidate Carbamide MPH Unclear Methylphenidate [3]
MR013387 Methylphenidate Ethylphenidate Unclear Methylphenidate [3]
MR013383 Methylphenidate p-Hydroxy-MPH Unclear Methylphenidate [3]
MR013382 Methylphenidate Ritalic acid Unclear Methylphenidate [3]
Other MR(s) Related to The Product of This MR
Other MR(s) That Metabolize The Produtc of This MR
MR ID Reactant Product MR Type Related Drug REF
MR013376 6-Oxo-MPH 6-Oxo-5(or 4)-Hydroxy-MPH Unclear Methylphenidate [3]
MR013380 6-Oxo-MPH 6-Oxo-ritalic acid Unclear Methylphenidate [3]
MR013373 6-Oxo-MPH p-Hydroxy-6-oxo-MPH Unclear Methylphenidate [3]
MR013370 6-Oxo-MPH Ritalic acid Unclear Methylphenidate [3]
References
1 Metabolism of methylphenidate in dog and rat
2 Methylphenidate is stereoselectively hydrolyzed by human carboxylesterase CES1A1. J Pharmacol Exp Ther. 2004 Aug;310(2):469-76.
3 Metabolomics of Methylphenidate and Ethylphenidate: Implications in Pharmacological and Toxicological Effects

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