KEGG   PATHWAY: his00982
Entry
his00982                    Pathway                                
Name
Drug metabolism - cytochrome P450 - Hermetia illucens (black soldier fly)
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
his00982  Drug metabolism - cytochrome P450
his00982

Organism
Hermetia illucens (black soldier fly) [GN:his]
Gene
119646741  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119657417  microsomal glutathione S-transferase 1-like isoform X1 [KO:K00799] [EC:2.5.1.18]
119657634  glutathione S-transferase theta-1-like [KO:K00799] [EC:2.5.1.18]
119657738  glutathione S-transferase theta-3 [KO:K00799] [EC:2.5.1.18]
119657985  glutathione S-transferase theta-3-like [KO:K00799] [EC:2.5.1.18]
119658236  prostaglandin E synthase-like [KO:K00799] [EC:2.5.1.18]
119658347  glutathione S-transferase E14 [KO:K00799] [EC:2.5.1.18]
119648229  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119648744  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119648745  glutathione S-transferase 1-like isoform X1 [KO:K00799] [EC:2.5.1.18]
119648746  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119648747  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119648748  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119648749  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119649263  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119659919  glutathione S-transferase 1 isoform X1 [KO:K00799] [EC:2.5.1.18]
119659930  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119659938  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119649467  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119649468  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119649709  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119649710  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119650050  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119650240  inactive glutathione S-transferase D3-like [KO:K00799] [EC:2.5.1.18]
119650963  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119651265  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119651266  glutathione S-transferase D1-like [KO:K00799] [EC:2.5.1.18]
119652625  glutathione S-transferase 1-1 [KO:K00799] [EC:2.5.1.18]
119652651  glutathione S-transferase D7 isoform X1 [KO:K00799] [EC:2.5.1.18]
119654705  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119654706  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119654707  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119654836  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119655113  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119655766  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
119657205  glutathione S-transferase theta-1-like [KO:K00799] [EC:2.5.1.18]
119656068  glutathione S-transferase [KO:K04097] [EC:5.3.99.2 2.5.1.18]
119657691  alcohol dehydrogenase class-3-like isoform X1 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
119657794  alcohol dehydrogenase class-3-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
119658051  alcohol dehydrogenase class-3-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
119656700  alcohol dehydrogenase class-3 [KO:K00121] [EC:1.1.1.284 1.1.1.1]
119646976  aldehyde dehydrogenase, dimeric NADP-preferring isoform X1 [KO:K00129] [EC:1.2.1.5]
119648758  UDP-glycosyltransferase UGT5 [KO:K00699] [EC:2.4.1.17]
119660056  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119660067  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119650123  UDP-glycosyltransferase UGT5-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119650142  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119650150  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119650155  UDP-glucosyltransferase 2-like [KO:K00699] [EC:2.4.1.17]
119661097  UDP-glycosyltransferase UGT4-like [KO:K00699] [EC:2.4.1.17]
119661099  UDP-glycosyltransferase UGT5-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119661157  UDP-glucosyltransferase 2-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119661231  UDP-glucosyltransferase 2-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119661741  UDP-glycosyltransferase UGT4-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119653869  UDP-glucosyltransferase 2-like isoform X1 [KO:K00699] [EC:2.4.1.17]
119653928  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119654243  UDP-glycosyltransferase UGT5 [KO:K00699] [EC:2.4.1.17]
119654563  UDP-glucosyltransferase 2-like [KO:K00699] [EC:2.4.1.17]
119655088  UDP-glucosyltransferase 2-like [KO:K00699] [EC:2.4.1.17]
119655089  UDP-glycosyltransferase UGT5-like [KO:K00699] [EC:2.4.1.17]
119655065  UDP-glucosyltransferase 2-like [KO:K00699] [EC:2.4.1.17]
119655873  UDP-glucosyltransferase 2-like [KO:K00699] [EC:2.4.1.17]
119646378  UDP-glycosyltransferase UGT5-like isoform X1 [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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