KEGG   PATHWAY: ocu00982
Entry
ocu00982                    Pathway                                
Name
Drug metabolism - cytochrome P450 - Oryctolagus cuniculus (rabbit)
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
ocu00982  Drug metabolism - cytochrome P450
ocu00982

Organism
Oryctolagus cuniculus (rabbit) [GN:ocu]
Gene
100352776  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100347582  putative dimethylaniline monooxygenase [N-oxide-forming] 6 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100353031  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100009119  FMO2; dimethylaniline monooxygenase [N-oxide-forming] 2 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100009065  FMO3; dimethylaniline monooxygenase [N-oxide-forming] 3 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100009120  FMO1; dimethylaniline monooxygenase [N-oxide-forming] 1 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100009064  FMO5; flavin-containing monooxygenase 5 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100009582  FMO4; dimethylaniline monooxygenase [N-oxide-forming] 4 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
100353174  glutathione S-transferase 3 isoform X1 [KO:K00799] [EC:2.5.1.18]
100353681  glutathione S-transferase alpha I isoform X2 [KO:K00799] [EC:2.5.1.18]
100353428  glutathione S-transferase Yc isoform X1 [KO:K00799] [EC:2.5.1.18]
100341104  glutathione S-transferase Yc isoform X1 [KO:K00799] [EC:2.5.1.18]
100353927  glutathione S-transferase alpha I isoform X1 [KO:K00799] [EC:2.5.1.18]
100354186  glutathione S-transferase A2 isoform X1 [KO:K00799] [EC:2.5.1.18]
100354436  glutathione S-transferase A4 [KO:K00799] [EC:2.5.1.18]
100341622  glutathione S-transferase A4 [KO:K00799] [EC:2.5.1.18]
100340711  glutathione S-transferase theta-3 isoform X1 [KO:K00799] [EC:2.5.1.18]
100338449  glutathione S-transferase theta-2B [KO:K00799] [EC:2.5.1.18]
100338194  LOW QUALITY PROTEIN: glutathione S-transferase theta-1 [KO:K00799] [EC:2.5.1.18]
100009073  GSTM2; glutathione S-transferase Mu 1 [KO:K00799] [EC:2.5.1.18]
100340829  microsomal glutathione S-transferase 1 [KO:K00799] [EC:2.5.1.18]
100356052  glutathione S-transferase Mu 3 [KO:K00799] [EC:2.5.1.18]
100357148  glutathione S-transferase Mu 7 isoform X2 [KO:K00799] [EC:2.5.1.18]
100328911  glutathione S-transferase Yc [KO:K00799] [EC:2.5.1.18]
100008879  MGST3; microsomal glutathione S-transferase 3 [KO:K00799] [EC:2.5.1.18]
103350707  LOW QUALITY PROTEIN: microsomal glutathione S-transferase 2 [KO:K00799] [EC:2.5.1.18]
100328910  glutathione S-transferase alpha I [KO:K00799] [EC:2.5.1.18]
100339996  LOW QUALITY PROTEIN: glutathione S-transferase Mu 1 [KO:K00799] [EC:2.5.1.18]
100357917  glutathione S-transferase Mu 1 isoform X1 [KO:K00799] [EC:2.5.1.18]
100358177  glutathione S-transferase Mu 1 isoform X1 [KO:K00799] [EC:2.5.1.18]
100349021  glutathione S-transferase omega-1 isoform X2 [KO:K00799] [EC:2.5.1.18]
100339842  glutathione S-transferase omega-2 [KO:K00799] [EC:2.5.1.18]
100340967  glutathione S-transferase theta-4 isoform X1 [KO:K00799] [EC:2.5.1.18]
127490035  glutathione S-transferase Yc-like isoform X1 [KO:K00799] [EC:2.5.1.18]
100342268  glutathione S-transferase P [KO:K23790] [EC:2.5.1.18]
100350399  glutathione S-transferase kappa 1 isoform X2 [KO:K13299] [EC:2.5.1.18]
100349830  glutathione S-transferase kappa 1 [KO:K13299] [EC:2.5.1.18]
100353701  hematopoietic prostaglandin D synthase [KO:K04097] [EC:5.3.99.2 2.5.1.18]
100009283  ADH1A; alcohol dehydrogenase 1 [KO:K13951] [EC:1.1.1.1]
100327260  ADH2-1; alcohol dehydrogenase class-2 isozyme 1 [KO:K13980] [EC:1.1.1.1]
100345521  ADH2-2; alcohol dehydrogenase class-2 isozyme 2 [KO:K13980] [EC:1.1.1.1]
100009307  ADH5; alcohol dehydrogenase class-3 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
100343992  alcohol dehydrogenase 6 [KO:K13952] [EC:1.1.1.1]
103346087  aldehyde dehydrogenase family 3 member B1 isoform X1 [KO:K00129] [EC:1.2.1.5]
127486711  aldehyde dehydrogenase family 3 member B2-like [KO:K00129] [EC:1.2.1.5]
100357007  amine oxidase [flavin-containing] B [KO:K00274] [EC:1.4.3.4]
100345623  amine oxidase [flavin-containing] A [KO:K00274] [EC:1.4.3.4]
100354428  AOX4; aldehyde oxidase 4 [KO:K00157] [EC:1.2.3.1]
100345417  AOX2; aldehyde oxidase 2 [KO:K00157] [EC:1.2.3.1]
100345675  AOX3; aldehyde oxidase 3 [KO:K00157] [EC:1.2.3.1]
100008601  AOX1; aldehyde oxidase 1 [KO:K00157] [EC:1.2.3.1]
127485684  aldehyde oxidase 3-like [KO:K00157] [EC:1.2.3.1]
127491577  aldehyde oxidase 1-like [KO:K00157] [EC:1.2.3.1]
100328586  UGT2B13; UDP-glucuronosyltransferase 2B13 precursor [KO:K00699] [EC:2.4.1.17]
100037707  UGT1A7; UDP glucuronosyltransferase 1 family, polypeptide A7 precursor [KO:K00699] [EC:2.4.1.17]
100037718  UGT1-6; UDP-glucuronosyltransferase 1-6 precursor [KO:K00699] [EC:2.4.1.17]
100009448  UGT2C1; UDP-glucuronosyltransferase 2C1 precursor [KO:K00699] [EC:2.4.1.17]
100328587  UGT2B16; UDP-glucuronosyltransferase 2B16 precursor [KO:K00699] [EC:2.4.1.17]
103352486  UDP-glucuronosyltransferase 1A4-like [KO:K00699] [EC:2.4.1.17]
100357464  UDP-glucuronosyltransferase 2B14 isoform X4 [KO:K00699] [EC:2.4.1.17]
100357038  UDP-glucuronosyltransferase 2B17 isoform X1 [KO:K00699] [EC:2.4.1.17]
100358969  UDP-glucuronosyltransferase 2A3 isoform X1 [KO:K00699] [EC:2.4.1.17]
100342219  UDP-glucuronosyltransferase 2B14 isoform X1 [KO:K00699] [EC:2.4.1.17]
100340772  UDP-glucuronosyltransferase 2B16 isoform X1 [KO:K00699] [EC:2.4.1.17]
100338508  UDP-glucuronosyltransferase 2B17 [KO:K00699] [EC:2.4.1.17]
100338077  UDP-glucuronosyltransferase 2B31 [KO:K00699] [EC:2.4.1.17]
100351592  UDP-glucuronosyltransferase 2A3 isoform X1 [KO:K00699] [EC:2.4.1.17]
100359229  UDP-glucuronosyltransferase 2A3 [KO:K00699] [EC:2.4.1.17]
100341030  LOW QUALITY PROTEIN: UDP-glucuronosyltransferase 2B16-like [KO:K00699] [EC:2.4.1.17]
108178122  UDP-glucuronosyltransferase 2B13 [KO:K00699] [EC:2.4.1.17]
100038310  UGT1-4; UDP-glucuronosyltransferase 1A4 precursor [KO:K00699] [EC:2.4.1.17]
100009057  UGT2B14; UDP-glucuronosyltransferase 2B14 precursor [KO:K00699] [EC:2.4.1.17]
108175478  UDP-glucuronosyltransferase 1A8-like [KO:K00699] [EC:2.4.1.17]
127482563  UDP-glucuronosyltransferase 2B14-like [KO:K00699] [EC:2.4.1.17]
127482767  UDP-glucuronosyltransferase 2B17-like isoform X1 [KO:K00699] [EC:2.4.1.17]
127490007  UDP-glucuronosyltransferase 2B14-like [KO:K00699] [EC:2.4.1.17]
100357720  UDP-glucuronosyltransferase 2B14 [KO:K00699] [EC:2.4.1.17]
108175393  UDP-glucuronosyltransferase 2B14 [KO:K00699] [EC:2.4.1.17]
100328937  cytochrome P450 1A2 [KO:K07409] [EC:1.14.14.1]
100342322  cytochrome P450 2E1 [KO:K07415] [EC:1.14.14.-]
100342572  cytochrome P450 2E1 [KO:K07415] [EC:1.14.14.-]
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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