General Information of This Metabolic Reaction (MR) (ID: MR011380)
Formula
SVG example
7-hydroxylation
Reactant Chlorpromazine Product Hydroxychlorpromazine
Reactant Info Product Info
Metabolic Enzyme Cytochrome P450 2D6 (CYP2D6) DME Info
Metabolic Type Oxidation - 7-hydroxylation
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
MR011381 Chlorpromazine Chlorpromazine-N-oxide Unclear - Unclear Chlorpromazine [1]
MR011382 Chlorpromazine Dedimethylchlorpromazine Unclear - Unclear Chlorpromazine [1]
MR011383 Chlorpromazine Demonomethylchlorpromazine Unclear - Unclear Chlorpromazine [1]
MR011384 Chlorpromazine Opromazine Oxidation - S-oxidation Chlorpromazine [2]
Other MR(s) Related to The Product of This MR
Other MR(s) That Produce The Product of This MR
MR ID Reactant Product MR Type Related Drug REF
MR000643 Chlorpromazine hydrochloride Hydroxychlorpromazine Oxidation - 7-Hydroxylation Chlorpromazine hydrochloride [3], [4]
MR002007 Perphenazine Hydroxychlorpromazine Oxidation - Hydroxylation Perphenazine [5]
References
1 DrugBank(Pharmacology-Metabolism):Chlorpromazine
2 Cytochrome P450 inactivation by pharmaceuticals and phytochemicals: therapeutic relevance Drug Metab Rev. 2008;40(1):101-47. doi: 10.1080/03602530701836704.
3 Classics in Chemical Neuroscience: Chlorpromazine ACS Chem Neurosci. 2019 Jan 16;10(1):79-88. doi: 10.1021/acschemneuro.8b00258.
4 Determination of chlorpromazine and its metabolites in animal-derived foods using QuEChERS-based extraction, EMR-Lipid cleanup, and UHPLC-Q-Orbitrap MS analysis. Food Chem. 2023 Mar 1;403:134298. doi: 10.1016/j.foodchem.2022.134298.
5 American Society of Health System Pharmacists; AHFS Drug Information 2010. Bethesda, MD. (2010), p. 2511

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