-
1
-
-
0035065393
-
Competitive CYP2C9 inhibitors: Enzyme inhibition studies, protein homology modeling and three-dimensional quantitative structure-activity relationship analysis
-
Afzelius L, Zamora I, Ridderstrom M, Andersson TB, Karlen A, and Masimirembwa CM (2001) Competitive CYP2C9 inhibitors: Enzyme inhibition studies, protein homology modeling and three-dimensional quantitative structure-activity relationship analysis. Mol Pharmacol 59:909-919.
-
(2001)
Mol Pharmacol
, vol.59
, pp. 909-919
-
-
Afzelius, L.1
Zamora, I.2
Ridderstrom, M.3
Andersson, T.B.4
Karlen, A.5
Masimirembwa, C.M.6
-
2
-
-
0035059352
-
Allosteric behavior in cytochrome P450-dependent in vitro drug-drug interactions: A prospective based on conformational dynamics
-
Atkins WM, Wang RW, and Lu AYH (2001) Allosteric behavior in cytochrome P450-dependent in vitro drug-drug interactions: A prospective based on conformational dynamics. Chem Res Toxicol 14:338-347.
-
(2001)
Chem Res Toxicol
, vol.14
, pp. 338-347
-
-
Atkins, W.M.1
Wang, R.W.2
Lu, A.Y.H.3
-
3
-
-
0031743851
-
Autoactivation and activation of the cytochrome P450s
-
Ekins S, Ring BJ, Binkley SN, Hall SD, and Wrighton SA (1998) Autoactivation and activation of the cytochrome P450s. Int J Clin Pharmacol Ther 36:642-651.
-
(1998)
Int J Clin Pharmacol Ther
, vol.36
, pp. 642-651
-
-
Ekins, S.1
Ring, B.J.2
Binkley, S.N.3
Hall, S.D.4
Wrighton, S.A.5
-
4
-
-
0029416939
-
N-Hydroxylation of dapsone by multiple enzymes of cytochrome P450: Implications for inhibition of haemotoxicity
-
Gill HJ, Tingle MD, and Park BK (1995) N-Hydroxylation of dapsone by multiple enzymes of cytochrome P450: Implications for inhibition of haemotoxicity. Br J Clin Pharmacol 40:531-538.
-
(1995)
Br J Clin Pharmacol
, vol.40
, pp. 531-538
-
-
Gill, H.J.1
Tingle, M.D.2
Park, B.K.3
-
5
-
-
0002888510
-
Human cytochrome P450 enzymes
-
(Ortiz de Montellano P ed), Plenum Press, New York
-
Guengerich FP (1995) Human cytochrome P450 enzymes, in Cytochrome P450: Structure, Mechanism and Biochemistry (Ortiz de Montellano P ed) pp 473-535, Plenum Press, New York.
-
(1995)
Cytochrome P450: Structure, Mechanism and Biochemistry
, pp. 473-535
-
-
Guengerich, F.P.1
-
6
-
-
0026562457
-
Site-directed mutagenesis of cytochrome P450s CYP2A1 and CYP2A2: Influence of the distal helix on the kinetics of testosterone hydroxylation
-
Hanioka N, Gonzalez FJ, Lindberg NA, Liu G, Gelhoin HV, and Korzekwa KR (1992) Site-directed mutagenesis of cytochrome P450s CYP2A1 and CYP2A2: Influence of the distal helix on the kinetics of testosterone hydroxylation. Biochemistry 31:3364-3370.
-
(1992)
Biochemistry
, vol.31
, pp. 3364-3370
-
-
Hanioka, N.1
Gonzalez, F.J.2
Lindberg, N.A.3
Liu, G.4
Gelhoin, H.V.5
Korzekwa, K.R.6
-
7
-
-
0032499691
-
Analysis of human cytochrome P450 3A4 cooperativity: Construction and characterization of a site-directed mutant that displays hyperbolic steroid hydroxylation kinetics
-
Harlow GR and Halpert JR (1998) Analysis of human cytochrome P450 3A4 cooperativity: Construction and characterization of a site-directed mutant that displays hyperbolic steroid hydroxylation kinetics. Proc Natl Acad Sci 95:6636-6641.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 6636-6641
-
-
Harlow, G.R.1
Halpert, J.R.2
-
8
-
-
0033485933
-
Structurul forms of phenprocoumon and warfarin that are metabolized at the active site of CYP2C9
-
He M, Korzekwa KR, Jones JP, Rettie AE, and Trager WF (1999) Structurul forms of phenprocoumon and warfarin that are metabolized at the active site of CYP2C9. Arch Biochem Biophys 372:16-28.
-
(1999)
Arch Biochem Biophys
, vol.372
, pp. 16-28
-
-
He, M.1
Korzekwa, K.R.2
Jones, J.P.3
Rettie, A.E.4
Trager, W.F.5
-
9
-
-
0034956877
-
Dapsone activation of CYP2C9-mediated metabolism: Evidence for activation of multiple substrates and a two-site model
-
Hutzler JM, Hauer MJ, and Tracy TS (2001) Dapsone activation of CYP2C9-mediated metabolism: Evidence for activation of multiple substrates and a two-site model. Drug Metab Dispos 29:1-6.
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 1-6
-
-
Hutzler, J.M.1
Hauer, M.J.2
Tracy, T.S.3
-
10
-
-
0030041933
-
Putative active site template model for cytochrome P4502C9 (tolbutamide hydroxylase)
-
Jones BC, Hawksworth G, Horne VA, Newlands A, Morsman J, Tute MS, and Smith DA (1996b) Putative active site template model for cytochrome P4502C9 (tolbutamide hydroxylase). Drug Metab Dispos 24:260-266.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 260-266
-
-
Jones, B.C.1
Hawksworth, G.2
Horne, V.A.3
Newlands, A.4
Morsman, J.5
Tute, M.S.6
Smith, D.A.7
-
11
-
-
0030053733
-
Three-dimensional quantitative structure-activity relationship for inhibitors of cytochrome P4502C9
-
Jones JP, He M, Trager WF, and Rettie AE (1996a) Three-dimensional quantitative structure-activity relationship for inhibitors of cytochrome P4502C9. Drug Metab Dispos 24:1-6.
-
(1996)
Drug Metab Dispos
, vol.24
, pp. 1-6
-
-
Jones, J.P.1
He, M.2
Trager, W.F.3
Rettie, A.E.4
-
12
-
-
0027411643
-
Predicting the cytochrome P450 mediated metabolism of xenobiotics
-
Korzekwa KR and Jones JP (1993) Predicting the cytochrome P450 mediated metabolism of xenobiotics. Pharmacogenetics 3:1-18.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 1-18
-
-
Korzekwa, K.R.1
Jones, J.P.2
-
13
-
-
0000574406
-
Evaluation of atypical cytochrome P450 kinetics with two-substrate models: Evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites
-
Korzekwa KR, Krishnamachary N, Shou M, Ogai A, Parise RA, Rettie AE, Gonzalez FJ, and Tracy TS (1998) Evaluation of atypical cytochrome P450 kinetics with two-substrate models: Evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites, Biochemistry 37:4137-4147.
-
(1998)
Biochemistry
, vol.37
, pp. 4137-4147
-
-
Korzekwa, K.R.1
Krishnamachary, N.2
Shou, M.3
Ogai, A.4
Parise, R.A.5
Rettie, A.E.6
Gonzalez, F.J.7
Tracy, T.S.8
-
14
-
-
0029128881
-
The substrate binding site of human liver cytochrome P450 2C9: An approach using designed tienilic acid derivatives and molecular modeling
-
Mancy A, Broto P, Dijols S, Dansette PM, and Mansuy D (1995) The substrate binding site of human liver cytochrome P450 2C9: An approach using designed tienilic acid derivatives and molecular modeling. Biochemistry 34:10365-10375.
-
(1995)
Biochemistry
, vol.34
, pp. 10365-10375
-
-
Mancy, A.1
Broto, P.2
Dijols, S.3
Dansette, P.M.4
Mansuy, D.5
-
15
-
-
0031841377
-
Cytochrome P4502C9: An enzyme of major importance in human drug metabolism
-
Miners JO and Birkett DJ (1998) Cytochrome P4502C9: An enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 45:525-538.
-
(1998)
Br J Clin Pharmacol
, vol.45
, pp. 525-538
-
-
Miners, J.O.1
Birkett, D.J.2
-
16
-
-
0032544220
-
Electron shuttle between membrane-bound cytochrome P450 3A4 and b5 rules uncoupling mechanisms
-
Perret A and Pompon D (1998) Electron shuttle between membrane-bound cytochrome P450 3A4 and b5 rules uncoupling mechanisms. Biochemistry 37:11412-11424.
-
(1998)
Biochemistry
, vol.37
, pp. 11412-11424
-
-
Perret, A.1
Pompon, D.2
-
17
-
-
0026519541
-
Hydroxylation of warfarin by human cDNA-expressed cytochrome P450: A role for P4502C9 in the etiology of (S)-warfarin-drug interactions
-
Rettie AE, Korzekwa KR, Kunze KL, Lawrence RF, Eddy AC, Aoyama T, Gelboin HV, Gonzalez FJ, and Trager WF (1992) Hydroxylation of warfarin by human cDNA-expressed cytochrome P450: A role for P4502C9 in the etiology of (S)-warfarin-drug interactions. Chem Res Toxicol 5:54-59.
-
(1992)
Chem Res Toxicol
, vol.5
, pp. 54-59
-
-
Gonzalez, F.J.1
Trager, W.F.2
-
18
-
-
0034696808
-
Arginines 97 and 108 in CYP2C9 are important determinants of the catalytic function
-
Ridderstrom M, Masimirembwa CM, Trump-Kallmeyer S, Ahlefelt M, Otter C, and Andersson TB (2000) Arginines 97 and 108 in CYP2C9 are important determinants of the catalytic function. Biochem Biophys Res Commun 270:983-987.
-
(2000)
Biochem Biophys Res Commun
, vol.270
, pp. 983-987
-
-
Ridderstrom, M.1
Masimirembwa, C.M.2
Trump-Kallmeyer, S.3
Ahlefelt, M.4
Otter, C.5
Andersson, T.B.6
-
19
-
-
0023949862
-
Modulation of rabbit and human hepatic cytochrome P-450-catalyzed steroid hydroxylations by α-naphthoflavone
-
Schwab GE, Raucy JL, and Johnson EF (1988) Modulation of rabbit and human hepatic cytochrome P-450-catalyzed steroid hydroxylations by α-naphthoflavone. Mol Pharmacol 33:493-499.
-
(1988)
Mol Pharmacol
, vol.33
, pp. 493-499
-
-
Schwab, G.E.1
Raucy, J.L.2
Johnson, E.F.3
-
21
-
-
0028307539
-
Activation of CYP3A4: Evidence for the simultaneous binding of two substrates in a cytochrome P450 active site
-
Shou M, Grogan J, Mancewicz JA, Krausz KW, Gonzalez FJ, Gelboin HV, and Korzekwa KR (1994) Activation of CYP3A4: Evidence for the simultaneous binding of two substrates in a cytochrome P450 active site. Biochemistry 33:6450-6455.
-
(1994)
Biochemistry
, vol.33
, pp. 6450-6455
-
-
Shou, M.1
Grogan, J.2
Mancewicz, J.A.3
Krausz, K.W.4
Gonzalez, F.J.5
Gelboin, H.V.6
Korzekwa, K.R.7
-
22
-
-
0002106247
-
Metabolically-based drug-drug interactions: Principles and mechanisms
-
(Levy RH, Thummel KE, Trager WF, Hansten PD, and Eichelbaum M eds), Lippincott Williams & Wilkins, Philadelphia
-
Thummel KE, Kunze KL, and Shen DD (2000) Metabolically-based drug-drug interactions: Principles and mechanisms, in Metabolic Drug Interactions (Levy RH, Thummel KE, Trager WF, Hansten PD, and Eichelbaum M eds) pp 3-19, Lippincott Williams & Wilkins, Philadelphia.
-
(2000)
Metabolic Drug Interactions
, pp. 3-19
-
-
Thummel, K.E.1
Kunze, K.L.2
Shen, D.D.3
-
23
-
-
0025801514
-
Tolbutamide and phenytoin hydroxylations by cDNA-expressed human liver cytochrome P4502C9
-
Veronese ME, Mackenzie PI, Doecke CJ, McManus ME, Miners JO, and Birkett DJ (1991) Tolbutamide and phenytoin hydroxylations by cDNA-expressed human liver cytochrome P4502C9. Biochem Biophys Res Commun 175:1112-1118.
-
(1991)
Biochem Biophys Res Commun
, vol.175
, pp. 1112-1118
-
-
Veronese, M.E.1
Mackenzie, P.I.2
Doecke, C.J.3
McManus, M.E.4
Miners, J.O.5
Birkett, D.J.6
-
24
-
-
0034093628
-
Human cytochrome P450 3A4: In vitro drug-drug interaction patterns are substrate-dependent
-
Wang RW, Newton DJ, Liu N, Atkins WM, and Lu AYH (2000) Human cytochrome P450 3A4: In vitro drug-drug interaction patterns are substrate-dependent. Drug Metab Dispos 28:360-366.
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 360-366
-
-
Wang, R.W.1
Newton, D.J.2
Liu, N.3
Atkins, W.M.4
Lu, A.Y.H.5
-
25
-
-
0033855822
-
CYP2C8/9 mediate dapsone N-hydroxylation at clinical concentrations of dapsone
-
Winter HR, Wang Y, and Unadkat JD (2000) CYP2C8/9 mediate dapsone N-hydroxylation at clinical concentrations of dapsone. Drug Metab Dispos 28:865-868.
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 865-868
-
-
Winter, H.R.1
Wang, Y.2
Unadkat, J.D.3
-
26
-
-
0026750647
-
The human hepatic cytochrome P450 involved in drug metabolism
-
Wrighton SA, and Stevens JC (1992) The human hepatic cytochrome P450 involved in drug metabolism. Crit Rev Toxicol 22:1-21.
-
(1992)
Crit Rev Toxicol
, vol.22
, pp. 1-21
-
-
Wrighton, S.A.1
Stevens, J.C.2
|