KEGG   PATHWAY: aoce00982
Entry
aoce00982                   Pathway                                
Name
Drug metabolism - cytochrome P450 - Amphiprion ocellaris (clown anemonefish)
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
aoce00982  Drug metabolism - cytochrome P450
aoce00982

Organism
Amphiprion ocellaris (clown anemonefish) [GN:aoce]
Gene
111577511  dimethylaniline monooxygenase [N-oxide-forming] 2-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
111577512  dimethylaniline monooxygenase [N-oxide-forming] 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
111577520  dimethylaniline monooxygenase [N-oxide-forming] 5-like isoform X1 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
111577525  dimethylaniline monooxygenase [N-oxide-forming] 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
111573627  microsomal glutathione S-transferase 2-like [KO:K00799] [EC:2.5.1.18]
111574660  microsomal glutathione S-transferase 3-like [KO:K00799] [EC:2.5.1.18]
111575699  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
111575710  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
111573058  glutathione S-transferase theta-1-like [KO:K00799] [EC:2.5.1.18]
111576129  glutathione S-transferase A-like isoform X1 [KO:K00799] [EC:2.5.1.18]
111576130  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111576131  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111576132  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111576133  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111576134  glutathione S-transferase A-like isoform X1 [KO:K00799] [EC:2.5.1.18]
111576135  glutathione S-transferase A-like isoform X1 [KO:K00799] [EC:2.5.1.18]
111572204  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111572205  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111572206  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111572207  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111581407  glutathione S-transferase 3-like [KO:K00799] [EC:2.5.1.18]
111586005  glutathione S-transferase Mu 3-like [KO:K00799] [EC:2.5.1.18]
111584020  glutathione S-transferase theta-3-like [KO:K00799] [EC:2.5.1.18]
111580714  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
111580715  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
111580716  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
111587350  mgst3; microsomal glutathione S-transferase 3 [KO:K00799] [EC:2.5.1.18]
111579282  mgst1; microsomal glutathione S-transferase 1 [KO:K00799] [EC:2.5.1.18]
111576124  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
111582043  glutathione S-transferase kappa 1-like [KO:K13299] [EC:2.5.1.18]
111576829  glutathione S-transferase kappa 1-like [KO:K13299] [EC:2.5.1.18]
111576831  glutathione S-transferase kappa 1-like [KO:K13299] [EC:2.5.1.18]
111562574  alcohol dehydrogenase class-3 chain L [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111562590  alcohol dehydrogenase 1-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111562591  alcohol dehydrogenase 1-like isoform X1 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111562592  alcohol dehydrogenase 1-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111562593  alcohol dehydrogenase 1-like isoform X1 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111588371  alcohol dehydrogenase class-3 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111588373  alcohol dehydrogenase class-3-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111568344  alcohol dehydrogenase 1-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
111568327  aldehyde dehydrogenase family 3 member B1-like isoform X1 [KO:K00129] [EC:1.2.1.5]
111578008  aldh3b1; aldehyde dehydrogenase family 3 member B1 [KO:K00129] [EC:1.2.1.5]
111581062  aldehyde dehydrogenase family 1 member A3-like [KO:K00129] [EC:1.2.1.5]
111563317  aldehyde dehydrogenase family 1 member A3-like [KO:K00129] [EC:1.2.1.5]
111563864  maob; amine oxidase [flavin-containing] B [KO:K00274] [EC:1.4.3.4]
111579096  probable flavin-containing monoamine oxidase A isoform X1 [KO:K00274] [EC:1.4.3.4]
111570749  aox1; aldehyde oxidase isoform X1 [KO:K00157] [EC:1.2.3.1]
111571828  UDP-glucuronosyltransferase-like [KO:K00699] [EC:2.4.1.17]
111565959  UDP-glucuronosyltransferase 1-2-like [KO:K00699] [EC:2.4.1.17]
111565989  UDP-glucuronosyltransferase 2C1-like [KO:K00699] [EC:2.4.1.17]
111580387  UDP-glucuronosyltransferase 2A1-like [KO:K00699] [EC:2.4.1.17]
111580425  UDP-glucuronosyltransferase 2A1-like isoform X1 [KO:K00699] [EC:2.4.1.17]
111580426  UDP-glucuronosyltransferase 2A1-like isoform X1 [KO:K00699] [EC:2.4.1.17]
111571303  UDP-glucuronosyltransferase 1-1-like [KO:K00699] [EC:2.4.1.17]
Compound
C01471  Acrolein
C01516  Morphine
C05011  Hydroxytamoxifen
C06174  Codeine
C06754  Chloroacetaldehyde
C06868  Carbamazepine
C07047  Ifosfamide
C07073  Lidocaine
C07108  Tamoxifen
C07163  Methadone
C07185  Valproic acid
C07492  Oxcarbazepine
C07493  10-Hydroxycarbazepine
C07495  Dihydroxycarbazepine
C07496  Carbamazepine-10,11-epoxide
C07501  Felbamate
C07572  Citalopram
C07643  4-Hydroxycyclophosphamide
C07644  4-Ketocyclophosphamide
C07645  Aldophosphamide
C07646  Carboxyphosphamide
C07647  Phosphoramide mustard
C07888  Cyclophosphamide
C08012  Levomethadyl acetate
C11004  2,6-Dimethylaniline
C11583  4-Glutathionyl cyclophosphamide
C11785  Normorphine
C16544  alpha-Hydroxytamoxifen
C16545  Tamoxifen N-oxide
C16546  N-Desmethyltamoxifen
C16547  Endoxifen
C16548  N,N-Didesmethyltamoxifen
C16549  alpha-Hydroxy-N-desmethyltamoxifen
C16550  Dechloroethylcyclophosphamide
C16551  Alcophosphamide
C16552  Nornitrogen mustard
C16553  4-Hydroxyifosfamide
C16554  4-Ketoifosfamide
C16555  2-Dechloroethylifosfamide
C16556  Aldoifosfamide
C16557  Carboxyifosfamide
C16558  Alcoifosfamide
C16559  Isophosphoramide mustard
C16560  3-Hydroxylidocaine
C16561  Monoethylglycinexylidide
C16569  Glycinexylidide
C16570  4-Hydroxy-2,6-dimethylaniline
C16571  2-Amino-3-methylbenzoate
C16572  3-Hydroxymonoethylglycinexylidide
C16576  Norcodeine
C16577  Codeine-6-glucuronide
C16578  Morphine-6-glucuronide
C16582  2-Hydroxyfelbamate
C16584  p-Hydroxyfelbamate
C16586  2-Phenyl-1,3-propanediol monocarbamate
C16587  3-Carbamoyl-2-phenylpropionaldehyde
C16591  3-Carbamoyl-2-phenylpropionic acid
C16592  Atropaldehyde
C16595  4-Hydroxy-5-phenyltetrahydro-1,3-oxazin-2-one
C16596  5-Phenyl-1,3-oxazinane-2,4-dione
C16601  2-Hydroxycarbamazepine
C16602  3-Hydroxycarbamazepine
C16603  2,3-Dihydroxycarbamazepine
C16604  2-Hydroxyiminostilbene
C16605  2H-Dibenz[b,f]azepin-2-one
C16606  Carbamazepine-o-quinone
C16607  Citalopram N-oxide
C16608  Demethylcitalopram
C16609  Didemethylcitalopram
C16610  Citalopram propionic acid
C16612  Citalopram aldehyde
C16643  Morphine-3-glucuronide
C16648  2-n-Propyl-4-pentenoic acid
C16649  4-Hydroxyvalproic acid
C16650  5-Hydroxyvalproic acid
C16651  3-Hydroxyvalproic acid
C16652  3-Oxovalproic acid
C16653  2-n-Propyl-2-pentenoic acid
C16654  2-n-Propyl-3-pentenoic acid
C16655  2-n-Propyl-4-oxopentanoic acid
C16656  2-Propyl-2,4-pentadienoic acid
C16657  2-Propylsuccinic acid
C16658  2-Propylglutaric acid
C16659  2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine
C16660  2-Ethyl-5-methyl-3,3-diphenyl-1-pyrroline
C16661  L-alpha-Acetyl-N-normethadol
C16662  L-alpha-Acetyl-N,N-dinormethadol
D00195  Codeine (USP)
D00252  Carbamazepine (JP18/USP/INN)
D00343  Ifosfamide (JAN/USP/INN)
D00358  Lidocaine (JP18/USP/INN)
D00399  Valproic acid (USP)
D00533  Oxcarbazepine (JAN/USP/INN)
D00536  Felbamate (USPINN)
D04716  Levomethadyl acetate (USAN)
D07704  Citalopram (USP/INN)
D07760  Cyclophosphamide (INN)
D08195  Methadone (BAN)
D08233  Morphine (BAN)
D08559  Tamoxifen (INN)
Reference
  Authors
Kato R, Kamatari T (eds).
  Title
[Drug Metabolism] (In Japanese)
  Journal
Tokyo Kagaku Dojin (2000)
Reference
  Authors
Gjerde J, Kisanga ER, Hauglid M, Holm PI, Mellgren G, Lien EA.
  Title
Identification and quantification of tamoxifen and four metabolites in serum by liquid chromatography-tandem mass spectrometry.
  Journal
J Chromatogr A 1082:6-14 (2005)
DOI:10.1016/j.chroma.2005.01.004
Reference
  Authors
Buck MB, Coller JK, Murdter TE, Eichelbaum M, Knabbe C.
  Title
TGFbeta2 and TbetaRII are valid molecular biomarkers for the antiproliferative effects of tamoxifen and tamoxifen metabolites in breast cancer cells.
  Journal
Breast Cancer Res Treat 107:15-24 (2008)
DOI:10.1007/s10549-007-9526-7
Reference
  Authors
Rodriguez-Antona C, Ingelman-Sundberg M.
  Title
Cytochrome P450 pharmacogenetics and cancer.
  Journal
Oncogene 25:1679-91 (2006)
DOI:10.1038/sj.onc.1209377
Reference
  Authors
Zhang J, Tian Q, Yung Chan S, Chuen Li S, Zhou S, Duan W, Zhu YZ.
  Title
Metabolism and transport of oxazaphosphorines and the clinical implications.
  Journal
Drug Metab Rev 37:611-703 (2005)
DOI:10.1080/03602530500364023
Reference
  Authors
Kosel M, Amey M, Aubert AC, Baumann P.
  Title
In vitro metabolism of citalopram by monoamine oxidase B in human blood.
  Journal
Eur Neuropsychopharmacol 11:75-8 (2001)
DOI:10.1016/S0924-977X(00)00128-0
Reference
  Authors
Olesen OV, Linnet K.
  Title
Studies on the stereoselective metabolism of citalopram by human liver microsomes and cDNA-expressed cytochrome P450 enzymes.
  Journal
Pharmacology 59:298-309 (1999)
DOI:10.1159/000028333
Reference
PMID:9698084
  Authors
Rochat B, Kosel M, Boss G, Testa B, Gillet M, Baumann P.
  Title
Stereoselective biotransformation of the selective serotonin reuptake inhibitor citalopram and its demethylated metabolites by monoamine oxidases in human liver.
  Journal
Biochem Pharmacol 56:15-23 (1998)
DOI:10.1016/S0006-2952(98)00008-2
Reference
  Authors
David AW, Thomas LL, William OF.
  Title
Foye's Principles of Medicinal Chemistry (5th ed)
  Journal
Lippincott Williams & Wilkins (2002)
Reference
  Authors
Oda Y, Kharasch ED.
  Title
Metabolism of methadone and levo-alpha-acetylmethadol (LAAM) by human intestinal cytochrome P450 3A4 (CYP3A4): potential contribution of intestinal metabolism to presystemic clearance and bioactivation.
  Journal
J Pharmacol Exp Ther 298:1021-32 (2001)
Reference
  Authors
Wang JS, Backman JT, Taavitsainen P, Neuvonen PJ, Kivisto KT.
  Title
Involvement of CYP1A2 and CYP3A4 in lidocaine N-deethylation and 3-hydroxylation in humans.
  Journal
Drug Metab Dispos 28:959-65 (2000)
Reference
  Authors
Dieckhaus CM, Thompson CD, Roller SG, Macdonald TL.
  Title
Mechanisms of idiosyncratic drug reactions: the case of felbamate.
  Journal
Chem Biol Interact 142:99-117 (2002)
DOI:10.1016/S0009-2797(02)00057-1
Reference
  Authors
Pearce RE, Lu W, Wang Y, Uetrecht JP, Correia MA, Leeder JS
  Title
Pathways of carbamazepine bioactivation in vitro. III. The role of human cytochrome P450 enzymes in the formation of 2,3-dihydroxycarbamazepine.
  Journal
Drug Metab Dispos 36:1637-49 (2008)
DOI:10.1124/dmd.107.019562
Reference
  Authors
Pearce RE, Vakkalagadda GR, Leeder JS.
  Title
Pathways of carbamazepine bioactivation in vitro I. Characterization of human cytochromes P450 responsible for the formation of 2- and 3-hydroxylated metabolites.
  Journal
Drug Metab Dispos 30:1170-9 (2002)
DOI:10.1124/dmd.30.11.1170
Reference
  Authors
Kumar S, Wong H, Yeung SA, Riggs KW, Abbott FS, Rurak DW.
  Title
Disposition of valproic acid in maternal, fetal, and newborn sheep. II: metabolism and renal elimination.
  Journal
Drug Metab Dispos 28:857-64 (2000)
Reference
  Authors
Bernad T, Joachim M.
  Title
Hydrolysis in Drug and Prodrug Metabolism: Chemistry, Biochemistry, and Enzymology
  Journal
Wiley-VCH (2003)
KO pathway
ko00982   
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