-
1
-
-
4243202809
-
3-Aminobenzanthrone, a human metabolite of the environmental pollutant 3-nitrobenzanthrone, forms DNA adducts after metabolic activation by human and rat liver microsomes: Evidence for activation by cytochrome P450 1A1 and P450 1A2
-
DOI 10.1021/tx049912v
-
Arlt VM, Hewer A, Sorg BL, Schmeiser HH, Phillips DH, and Stiborova M (2004) 3-Aminobenzanthrone, a human metabolite of the environmental pollutant 3-nitrobenzanthrone, forms DNA adducts after metabolic activation by human and rat liver microsomes: evidence for activation by cytochrome P450 1A1 and P450 1A2. Chem Res Toxicol 17:1092-1101. (Pubitemid 39108677)
-
(2004)
Chemical Research in Toxicology
, vol.17
, Issue.8
, pp. 1092-1101
-
-
Arlt, V.M.1
Hewer, A.2
Sorg, B.L.3
Schmeiser, H.H.4
Phillips, D.H.5
Stiborova, M.6
-
2
-
-
0037939783
-
Human enzymes involved in the metabolic activation of the environmental contaminant 3-nitrobenzanthrone: Evidence for reductive activation by human NADPH:Cytochrome P450 reductase
-
Arlt VM, Stiborova M, Hewer A, Schmeiser HH, and Phillips DH (2003) Human enzymes involved in the metabolic activation of the environmental contaminant 3-nitrobenzanthrone: evidence for reductive activation by human NADPH:cytochrome P450 reductase. Cancer Res 63:2752-2761. (Pubitemid 36667145)
-
(2003)
Cancer Research
, vol.63
, Issue.11
, pp. 2752-2761
-
-
Arlt, V.M.1
Stiborova, M.2
Hewer, A.3
Schmeiser, H.H.4
Phillips, D.H.5
-
3
-
-
0142188770
-
Correlation of CYP2D6 genotype with perhexiline phenotypic metabolizer status
-
DOI 10.1097/00008571-200310000-00006
-
Barclay ML, Sawyers SM, Begg EJ, Zhang M, Roberts RL, Kennedy MA, and Elliott JM (2003) Correlation of CYP2D6 genotype with perhexiline phenotypic metabolizer status. Pharmacogenetics 13:627-632. (Pubitemid 37311149)
-
(2003)
Pharmacogenetics
, vol.13
, Issue.10
, pp. 627-632
-
-
Barclay, M.L.1
Sawyers, S.M.2
Begg, E.J.3
Zhang, M.4
Roberts, R.L.5
Kennedy, M.A.6
Elliott, J.M.7
-
4
-
-
0031405796
-
Quick onset of severe abdominal pain after codeine in an ultrarapid metabolizer of debrisoquine
-
Dalén P, Frengell C, Dahl ML, and Sjöqvist F (1997) Quick onset of severe abdominal pain after codeine in an ultrarapid metabolizer of debrisoquine. Ther Drug Monit 19:543-544.
-
(1997)
Ther Drug Monit
, vol.19
, pp. 543-544
-
-
Dalén, P.1
Frengell, C.2
Dahl, M.L.3
Sjöqvist, F.4
-
5
-
-
0033529017
-
Novel approach to predicting P450-mediated drug metabolism: Development of a combined protein and pharmacophore model for CYP2D6
-
DOI 10.1021/jm981118h
-
de Groot MJ, Ackland MJ, Horne VA, Alex AA, and Jones BC (1999) Novel approach to predicting P450-mediated drug metabolism: development of a combined protein and pharmacophore model for CYP2D6. J Med Chem 42:1515-1524. (Pubitemid 29226723)
-
(1999)
Journal of Medicinal Chemistry
, vol.42
, Issue.9
, pp. 1515-1524
-
-
De Groot, M.J.1
Ackland, M.J.2
Horne, V.A.3
Alex, A.A.4
Jones, B.C.5
-
6
-
-
0029995711
-
A three-dimensional protein model for human cytochrome P450 2D6 based on the crystal structures of P450 101, P450 102, and P450 108
-
DOI 10.1021/tx960003i
-
de Groot MJ, Vermeulen NP, Kramer JD, van Acker FA, and Donné-Op den Kelder GM (1996) A three-dimensional protein model for human cytochrome P450 2D6 based on the crystal structures of P450 101, P450 102, and P450 108. Chem Res Toxicol 9:1079-1091. (Pubitemid 26347960)
-
(1996)
Chemical Research in Toxicology
, vol.9
, Issue.7
, pp. 1079-1091
-
-
De Groot, M.J.1
Vermeulen, N.P.E.2
Kramer, J.D.3
Van Acker, F.A.A.4
Donne-Op, D.K.G.M.5
-
7
-
-
0033967525
-
Theoretical investigation of substrate specificity for cytochromes P450 IA2, P450 IID6 and P450 IIIA4
-
DOI 10.1023/A:1008187802746
-
De Rienzo F, Fanelli F, Menziani MC, and De Benedetti PG (2000) Theoretical investigation of substrate specificity for cytochromes P450 IA2, P450 IID6 and P450 IIIA4. J Comput Aided Mol Des 14:93-116. (Pubitemid 30103825)
-
(2000)
Journal of Computer-Aided Molecular Design
, vol.14
, Issue.1
, pp. 93-116
-
-
De Rienzo, F.1
Fanelli, F.2
Menziani, M.C.3
De Benedetti, P.G.4
-
8
-
-
1542329740
-
Tizanidine is mainly metabolized by cytochrome P450 1A2 in vitro
-
DOI 10.1046/j.1365-2125.2003.02028.x
-
Granfors MT, Backman JT, Laitila J, and Neuvonen PJ (2004) Tizanidine is mainly metabolized by cytochrome P450 1A2 in vitro. Br J Clin Pharmacol 57:349-353. (Pubitemid 38296999)
-
(2004)
British Journal of Clinical Pharmacology
, vol.57
, Issue.3
, pp. 349-353
-
-
Granfors, M.T.1
Backman, J.T.2
Laitila, J.3
Neuvonen, P.J.4
-
9
-
-
0030221210
-
The role of cytochrome P450 2D6 in the metabolism of moclobemide
-
Härtter S, Dingemanse J, Baier D, Ziegler G, and Hiemke C (1996) The role of cytochrome P450 2D6 in the metabolism of moclobemide. Eur Neuropsychopharmacol 6:225-230. (Pubitemid 26281561)
-
(1996)
European Neuropsychopharmacology
, vol.6
, Issue.3
, pp. 225-230
-
-
Hartter, S.1
Dingemanse, J.2
Baier, D.3
Ziegler, G.4
Hiemke, C.5
-
10
-
-
0026046988
-
A three-dimensional molecular template for substrates of human cytochrome P450 involved in debrisoquine 4-hydroxylation
-
Islam SA, Wolf CR, Lennard MS, and Sternberg MJ (1991) A three-dimensional molecular template for substrates of human cytochrome P450 involved in debrisoquine 4-hydroxylation. Carcinogenesis 12:2211-2219.
-
(1991)
Carcinogenesis
, vol.12
, pp. 2211-2219
-
-
Islam, S.A.1
Wolf, C.R.2
Lennard, M.S.3
Sternberg, M.J.4
-
11
-
-
0030069518
-
Metabolism of 5-methylchrysene and 6-methylchrysene by human hepatic and pulmonary cytochrome P450 enzymes
-
Koehl W, Amin S, Staretz ME, Ueng YF, Yamazaki H, Tateishi T, Guengerich FP, and Hecht SS (1996) Metabolism of 5-methylchrysene and 6-methylchrysene by human hepatic and pulmonary cytochrome P450 enzymes. Cancer Res 56:316-324. (Pubitemid 26026360)
-
(1996)
Cancer Research
, vol.56
, Issue.2
, pp. 316-324
-
-
Koehl, W.1
Amin, S.2
Staretz, M.E.3
Ueng, Y.-F.4
Yamazaki, H.5
Tateishi, T.6
Guengerich, F.P.7
Hecht, S.S.8
-
12
-
-
80052572983
-
Development of two-dimensional template system for the prediction of CYP2B6-mediated reaction sites
-
Koyama N and Yamazoe Y (2011) Development of two-dimensional template system for the prediction of CYP2B6-mediated reaction sites. Drug Metab Pharmacokinet 26:309-330.
-
(2011)
Drug Metab Pharmacokinet
, vol.26
, pp. 309-330
-
-
Koyama, N.1
Yamazoe, Y.2
-
13
-
-
0026553661
-
A predictive model for substrates of cytochrome P450-debrisoquine (2D6)
-
Koymans L, Vermeulen NP, van Acker SA, te Koppele JM, Heykants JJ, Lavrijsen K, Meuldermans W, and Donné-Op den Kelder GM (1992) A predictive model for substrates of cytochrome P450-debrisoquine (2D6). Chem Res Toxicol 5:211-219.
-
(1992)
Chem Res Toxicol
, vol.5
, pp. 211-219
-
-
Koymans, L.1
Vermeulen, N.P.2
Van Acker, S.A.3
Te Koppele, J.M.4
Heykants, J.J.5
Lavrijsen, K.6
Meuldermans, W.7
Donné-Op Den Kelder, G.M.8
-
14
-
-
0033607201
-
Diclofenac and its derivatives as tools for studying human cytochromes P450 active sites: Particular efficiency and regioselectivity of P450 2Cs
-
Mancy A, Antignac M, Minoletti C, Dijols S, Mouries V, Duong NT, Battioni P, Dansette PM, and Mansuy D (1999) Diclofenac and its derivatives as tools for studying human cytochromes P450 active sites: particular efficiency and regioselectivity of P450 2Cs. Biochemistry 38: 14264-14270.
-
(1999)
Biochemistry
, vol.38
, pp. 14264-14270
-
-
Mancy, A.1
Antignac, M.2
Minoletti, C.3
Dijols, S.4
Mouries, V.5
Duong, N.T.6
Battioni, P.7
Dansette, P.M.8
Mansuy, D.9
-
15
-
-
79955670192
-
In vitro characterization of the cytochrome P450 isoforms involved in the metabolism of 6-methoxy-2-napthylacetic acid, an active metabolite of the prodrug nabumetone
-
Matsumoto K, Nemoto E, Hasegawa T, Akimoto M, and Sugibayashi K (2011) In vitro characterization of the cytochrome P450 isoforms involved in the metabolism of 6-methoxy-2-napthylacetic acid, an active metabolite of the prodrug nabumetone. Biol Pharm Bull 34:734-739.
-
(2011)
Biol Pharm Bull
, vol.34
, pp. 734-739
-
-
Matsumoto, K.1
Nemoto, E.2
Hasegawa, T.3
Akimoto, M.4
Sugibayashi, K.5
-
16
-
-
0022899555
-
The molecular mechanisms of two common polymorphisms of drug oxidation - Evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation
-
Meyer UA, Gut J, Kronbach T, Skoda C, Meier UT, Catin T, and Dayer P (1986) The molecular mechanisms of two common polymorphisms of drug oxidation: evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation. Xenobiotica 16:449-464. (Pubitemid 16076723)
-
(1986)
Xenobiotica
, vol.16
, Issue.5
, pp. 449-464
-
-
Meyer, U.A.1
Gut, J.2
Kronbach, T.3
-
17
-
-
80052380142
-
Structure-based site of metabolism prediction for cytochrome P450 2D6
-
Moors SL, Vos AM, Cummings MD, Van Vlijmen H, and Ceulemans A (2011) Structure-based site of metabolism prediction for cytochrome P450 2D6. J Med Chem 54:6098-6105.
-
(2011)
J Med Chem
, vol.54
, pp. 6098-6105
-
-
Moors, S.L.1
Vos, A.M.2
Cummings, M.D.3
Van Vlijmen, H.4
Ceulemans, A.5
-
18
-
-
33750608093
-
CYP2A13 expressed in human bladder metabolically activates 4-aminobiphenyl
-
DOI 10.1002/ijc.22136
-
Nakajima M, Itoh M, Sakai H, Fukami T, Katoh M, Yamazaki H, Kadlubar FF, Imaoka S, Funae Y, and Yokoi T (2006) CYP2A13 expressed in human bladder metabolically activates 4-aminobiphenyl. Int J Cancer 119:2520-2526. (Pubitemid 44691304)
-
(2006)
International Journal of Cancer
, vol.119
, Issue.11
, pp. 2520-2526
-
-
Nakajima, M.1
Itoh, M.2
Sakai, H.3
Fukami, T.4
Katoh, M.5
Yamazaki, H.6
Kadlubar, F.F.7
Imaoka, S.8
Funae, Y.9
Yokoi, T.10
-
19
-
-
0031047813
-
Toluene metabolism by cDNA-expressed human hepatic cytochrome P450
-
DOI 10.1016/S0006-2952(96)00652-1, PII S0006295296006521
-
Nakajima T, Wang RS, Elovaara E, Gonzalez FJ, Gelboin HV, Raunio H, Pelkonen O, Vainio H, and Aoyama T (1997) Toluene metabolism by cDNA-expressed human hepatic cytochrome P450. Biochem Pharmacol 53:271-277. (Pubitemid 27112943)
-
(1997)
Biochemical Pharmacology
, vol.53
, Issue.3
, pp. 271-277
-
-
Nakajima, T.1
Wang, R.-S.2
Elovaara, E.3
Gonzalez, F.J.4
Gelboin, H.V.5
Raunio, H.6
Pelkonen, O.7
Vainio, H.8
Aoyama, T.9
-
20
-
-
0032812611
-
An inhibitory monoclonal antibody to human cytochrome P450 2A6 defines its role in the metabolism of coumarin, 7-ethoxycoumarin and 4-nitroanisole in human liver
-
Sai Y, Yang TJ, Krausz KW, Gonzalez FJ, and Gelboin HV (1999) An inhibitory monoclonal antibody to human cytochrome P450 2A6 defines its role in the metabolism of coumarin, 7-ethoxycoumarin and 4-nitroanisole in human liver. Pharmacogenetics 9:229-237. (Pubitemid 29359005)
-
(1999)
Pharmacogenetics
, vol.9
, Issue.2
, pp. 229-237
-
-
Sai, Y.1
Jian, Y.T.2
Krausz, K.W.3
Gonzalez, F.J.4
Gelboin, H.V.5
-
21
-
-
1242276393
-
Inhibitory Effects of the Monoamine Oxidase Inhibitor Tranylcypromine on the Cytochrome P450 Enzymes CYP2C19, CYP2C9, and CYP2D6
-
DOI 10.1023/B:CEMN.0000012725.31108.4a
-
Salsali M, Holt A, and Baker GB (2004) Inhibitory effects of the monoamine oxidase inhibitor tranylcypromine on the cytochrome P450 enzymes CYP2C19, CYP2C9, and CYP2D6. Cell Mol Neurobiol 24:63-76. (Pubitemid 38233730)
-
(2004)
Cellular and Molecular Neurobiology
, vol.24
, Issue.1
, pp. 63-76
-
-
Salsali, M.1
Holt, A.2
Baker, G.B.3
-
22
-
-
0032870308
-
Multiple cytochrome P-450s involved in the metabolism of terbinafine suggest a limited potential for drug-drug interactions
-
Vickers AE, Sinclair JR, Zollinger M, Heitz F, Glänzel U, Johanson L, and Fischer V (1999) Multiple cytochrome P-450s involved in the metabolism of terbinafine suggest a limited potential for drug-drug interactions. Drug Metab Dispos 27:1029-1038. (Pubitemid 29409639)
-
(1999)
Drug Metabolism and Disposition
, vol.27
, Issue.9
, pp. 1029-1038
-
-
Vickers, A.E.M.1
Sinclair, J.R.2
Zollinger, M.3
Heitz, F.4
Glanzel, U.5
Johanson, L.6
Fischer, V.7
-
23
-
-
6944221357
-
1/AUC) ratios
-
DOI 10.1124/dmd.104.000794
-
Williams JA, Hyland R, Jones BC, Smith DA, Hurst S, Goosen TC, Peterkin V, Koup JR, and Ball SE (2004) Drug-drug interactions for UDP- glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios. Drug Metab Dispos 32:1201-1208. (Pubitemid 39410902)
-
(2004)
Drug Metabolism and Disposition
, vol.32
, Issue.11
, pp. 1201-1208
-
-
Williams, J.A.1
Hyland, R.2
Jones, B.C.3
Smith, D.A.4
Hurst, S.5
Goosen, T.C.6
Peterkin, V.7
Koup, J.R.8
Ball, S.E.9
-
24
-
-
0021884394
-
Substrate specificity of human liver cytochrome P-450 debrisoquine 4-hydroxylase probed using immunochemical inhibition and chemical modeling
-
Wolff T, Distlerath LM, Worthington MT, Groopman JD, Hammons GJ, Kadlubar FF, Prough RA, Martin MV, and Guengerich FP (1985) Substrate specificity of human liver cytochrome P-450 debrisoquine 4-hydroxylase probed using immunochemical inhibition and chemical modeling. Cancer Res 45:2116-2122. (Pubitemid 15024394)
-
(1985)
Cancer Research
, vol.45
, Issue.5
, pp. 2116-2122
-
-
Wolff, T.1
Distlerath, L.M.2
Worthington, M.T.3
-
25
-
-
80052603590
-
Predicting oxidation sites with order of occurrence among multiple sites for CYP4A-mediated reactions
-
Yamaura Y, Yoshinari K, and Yamazoe Y (2011) Predicting oxidation sites with order of occurrence among multiple sites for CYP4A-mediated reactions. Drug Metab Pharmacokinet 26:351-363.
-
(2011)
Drug Metab Pharmacokinet
, vol.26
, pp. 351-363
-
-
Yamaura, Y.1
Yoshinari, K.2
Yamazoe, Y.3
-
26
-
-
0030064194
-
7-Ethoxycoumarin O-deethylation catalyzed by cytochromes P450 1A2 and 2E1 in human liver microsomes
-
DOI 10.1016/0006-2952(95)02178-7
-
Yamazaki H, Inoue K, Mimura M, Oda Y, Guengerich FP, and Shimada T (1996) 7-Ethoxy-coumarin O-deethylation catalyzed by cytochromes P450 1A2 and 2E1 in human liver microsomes. Biochem Pharmacol 51:313-319. (Pubitemid 26054438)
-
(1996)
Biochemical Pharmacology
, vol.51
, Issue.3
, pp. 313-319
-
-
Yamazaki, H.1
Inoue, K.2
Mimura, M.3
Oda, Y.4
Guengerich, F.P.5
Shimada, T.6
-
27
-
-
80054955875
-
Construction of a CYP2E1-template system for prediction of the metabolism on both site and preference order
-
Yamazoe Y, Ito K, and Yoshinari K (2011) Construction of a CYP2E1-template system for prediction of the metabolism on both site and preference order. Drug Metab Rev 43:409-439.
-
(2011)
Drug Metab Rev
, vol.43
, pp. 409-439
-
-
Yamazoe, Y.1
Ito, K.2
Yoshinari, K.3
|