-
1
-
-
0034541821
-
The human CYP3A subfamily: Practical considerations
-
Wrighton S.A., et al. The human CYP3A subfamily: practical considerations. Drug Metab. Rev. 32:2000;339-361.
-
(2000)
Drug Metab. Rev.
, vol.32
, pp. 339-361
-
-
Wrighton, S.A.1
-
2
-
-
0035071598
-
Sequence diversity in CYP3A promotors and characterization of the genetic basis of polymorphic CYP3A5 expression
-
Kuehl P., et al. Sequence diversity in CYP3A promotors and characterization of the genetic basis of polymorphic CYP3A5 expression. Nat. Genet. 27:2001;383-391.
-
(2001)
Nat. Genet.
, vol.27
, pp. 383-391
-
-
Kuehl, P.1
-
3
-
-
0035135258
-
CDNA cloning and initial characterization of CYP3A43, a novel human cytochrome P450
-
Domanski T.L., et al. cDNA cloning and initial characterization of CYP3A43, a novel human cytochrome P450. Mol. Pharmacol. 59:2001;386-392.
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 386-392
-
-
Domanski, T.L.1
-
4
-
-
0036028389
-
Design and application of fluorimetric assays for human cytochrome P450 inhibition
-
Crespi C.L., et al. Design and application of fluorimetric assays for human cytochrome P450 inhibition. Methods Enzymol. 357:2002;276-284.
-
(2002)
Methods Enzymol.
, vol.357
, pp. 276-284
-
-
Crespi, C.L.1
-
5
-
-
0033664783
-
Substrate-dependent modeulation of CYP3A4 catalytic activity: Analysis of 27 test compounds with four fluorimetric substrates
-
Stresser D.M., et al. Substrate-dependent modeulation of CYP3A4 catalytic activity: analysis of 27 test compounds with four fluorimetric substrates. Drug Metab. Dispos. 28:2000;1440-1448.
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 1440-1448
-
-
Stresser, D.M.1
-
7
-
-
0034458681
-
Present and future in vitro approaches for drug metabolism
-
Ekins S., et al. Present and future in vitro approaches for drug metabolism. J. Pharmacol. Toxicol. Methods. 44:2000;313-324.
-
(2000)
J. Pharmacol. Toxicol. Methods
, vol.44
, pp. 313-324
-
-
Ekins, S.1
-
8
-
-
0001244698
-
In vitro metabolism: Subcellular fractions
-
T.F. et al. Woolf. Marcel Dekker
-
Ekins S., et al. In vitro metabolism: subcellular fractions. Woolf T.F., et al. Handbook of Drug Metabolism. 1999;363-399 Marcel Dekker.
-
(1999)
Handbook of Drug Metabolism
, pp. 363-399
-
-
Ekins, S.1
-
9
-
-
0036201594
-
Atypical kinetic profiles in drug metabolism reactions
-
Hutzler J.M., Tracy T.S. Atypical kinetic profiles in drug metabolism reactions. Drug Metab. Dispos. 30:2002;355-362.
-
(2002)
Drug Metab. Dispos.
, vol.30
, pp. 355-362
-
-
Hutzler, J.M.1
Tracy, T.S.2
-
10
-
-
0000574406
-
Evaluation of atypical cytochrome P450 kinetics with two-substrate-models: Evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites
-
Korzekwa K.R., et al. Evaluation of atypical cytochrome P450 kinetics with two-substrate-models: evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites. Biochemistry. 37:1998;4137-4147.
-
(1998)
Biochemistry
, vol.37
, pp. 4137-4147
-
-
Korzekwa, K.R.1
-
11
-
-
0031743851
-
Autoactivation and activation of cytochrome P450s
-
Ekins S., et al. Autoactivation and activation of cytochrome P450s. Int. J. Clin. Pharmacol. Ther. 36:1998;642-651.
-
(1998)
Int. J. Clin. Pharmacol. Ther.
, vol.36
, pp. 642-651
-
-
Ekins, S.1
-
12
-
-
0031960329
-
Human cytochrome P4503A (CYP3A) mediated midazolam metabolism: The effect of assay conditions and regioselective stimulation by a-napthoflavone, terfenadine and testosterone
-
Maenpaa J., et al. Human cytochrome P4503A (CYP3A) mediated midazolam metabolism: the effect of assay conditions and regioselective stimulation by a-napthoflavone, terfenadine and testosterone. Pharmacogenetics. 8:1998;137-155.
-
(1998)
Pharmacogenetics
, vol.8
, pp. 137-155
-
-
Maenpaa, J.1
-
14
-
-
0034093628
-
Human cytochrome P-450 3A4: In vitro drug-drug interaction patterns are substrate-dependent
-
Wang R.W., et al. Human cytochrome P-450 3A4: in vitro drug-drug interaction patterns are substrate-dependent. Drug Metab. Dispos. 28:2000;360-366.
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 360-366
-
-
Wang, R.W.1
-
15
-
-
0032735988
-
CYP3A4 drug interactions: Correlation of ten in vitro probe substrates
-
Kenworthy K.E., et al. CYP3A4 drug interactions: correlation of ten in vitro probe substrates. Br. J. Clin. Pharmacol. 48:1999;716-727.
-
(1999)
Br. J. Clin. Pharmacol.
, vol.48
, pp. 716-727
-
-
Kenworthy, K.E.1
-
16
-
-
0035964178
-
Phenylalanine and tryptophan scanning mutagenesis of CYP3A4 substrate recognition site residues and effect on substrate oxidation and cooperativity
-
Domanski T.L., et al. Phenylalanine and tryptophan scanning mutagenesis of CYP3A4 substrate recognition site residues and effect on substrate oxidation and cooperativity. Biochemistry. 40:2001;10150-10160.
-
(2001)
Biochemistry
, vol.40
, pp. 10150-10160
-
-
Domanski, T.L.1
-
17
-
-
0034705191
-
Elucidation of distinct ligand binding sites for the cytochrome P450 3A4
-
Hosea N.A., et al. Elucidation of distinct ligand binding sites for the cytochrome P450 3A4. Biochemistry. 39:2000;5929-5939.
-
(2000)
Biochemistry
, vol.39
, pp. 5929-5939
-
-
Hosea, N.A.1
-
18
-
-
0028307539
-
Activation of CYP3A4: Evidence for the simultaneous binding of two substrates in a cytochrome P450 active site
-
Shou M., et al. Activation of CYP3A4: evidence for the simultaneous binding of two substrates in a cytochrome P450 active site. Biochemistry. 33:1994;6450-6455.
-
(1994)
Biochemistry
, vol.33
, pp. 6450-6455
-
-
Shou, M.1
-
19
-
-
0035910579
-
A kinetic model for the metabolic interaction of the two substrates at the active site of cytochrome P450 3A4
-
Shou M., et al. A kinetic model for the metabolic interaction of the two substrates at the active site of cytochrome P450 3A4. J. Biol. Chem. 276:2001;2256-2262.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 2256-2262
-
-
Shou, M.1
-
20
-
-
27244462157
-
Covalent alteration of the CYP3A4 active site: Evidence for multiple substrate binding domains
-
Schrag M.L., Wienkers L.C. Covalent alteration of the CYP3A4 active site: evidence for multiple substrate binding domains. Arch. Biochem. Biophys. 391:2001;49-55.
-
(2001)
Arch. Biochem. Biophys.
, vol.391
, pp. 49-55
-
-
Schrag, M.L.1
Wienkers, L.C.2
-
21
-
-
0031824305
-
Analysis of four residues within substrate recognition site 4 of human cytochrome P450 3A4: Role in steroid hydroxylase activity and α-napthoflavone stimulation
-
Domanski T.L., et al. Analysis of four residues within substrate recognition site 4 of human cytochrome P450 3A4: role in steroid hydroxylase activity and α-napthoflavone stimulation. Arch. Biochem. Biophys. 350:1998;223-232.
-
(1998)
Arch. Biochem. Biophys.
, vol.350
, pp. 223-232
-
-
Domanski, T.L.1
-
22
-
-
0032822383
-
Three dimensional quantitative structure activity relationship (3D-QSAR) analysis of CYP3A4 substrates
-
Ekins S., et al. Three dimensional quantitative structure activity relationship (3D-QSAR) analysis of CYP3A4 substrates. J. Pharmacol. Exp. Ther. 291:1999;424-433.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.291
, pp. 424-433
-
-
Ekins, S.1
-
23
-
-
0031581857
-
Drug-drug interactions: Effect of quinidine on nifedipine binding to human cytochrome P450 3A4
-
Koley A.P., et al. Drug-drug interactions: effect of quinidine on nifedipine binding to human cytochrome P450 3A4. Biochem. Pharmacol. 53:1997;455-460.
-
(1997)
Biochem. Pharmacol.
, vol.53
, pp. 455-460
-
-
Koley, A.P.1
-
24
-
-
0035059352
-
Allosteric behavior in cytochrome P450-dependent in vitro drug-drug interactions: A prospective based on conformational dyamics
-
Atkins W.M., et al. Allosteric behavior in cytochrome P450-dependent in vitro drug-drug interactions: A prospective based on conformational dyamics. Chem. Res. Toxicol. 14:2001;338-347.
-
(2001)
Chem. Res. Toxicol.
, vol.14
, pp. 338-347
-
-
Atkins, W.M.1
-
25
-
-
0036589360
-
Towards a new age of virtual ADME/TOX and multidimensional drug discovery
-
Ekins S., et al. Towards a new age of virtual ADME/TOX and multidimensional drug discovery. J. Comput. Aided Mol. Des. 16:2002;381-401.
-
(2002)
J. Comput. Aided Mol. Des.
, vol.16
, pp. 381-401
-
-
Ekins, S.1
-
26
-
-
0036135405
-
In silico ADME/TOX: The state of the art at the 220th ACS meeting
-
Ekins S., Rose J.P. In silico ADME/TOX: the state of the art at the 220th ACS meeting. J. Mol. Graph. 20:2002;305-309.
-
(2002)
J. Mol. Graph.
, vol.20
, pp. 305-309
-
-
Ekins, S.1
Rose, J.P.2
-
27
-
-
0034460173
-
Progress in predicting human ADME parameters in silico
-
Ekins S., et al. Progress in predicting human ADME parameters in silico. J. Pharmacol. Toxicol. Methods. 44:2000;251-272.
-
(2000)
J. Pharmacol. Toxicol. Methods
, vol.44
, pp. 251-272
-
-
Ekins, S.1
-
28
-
-
0002510887
-
Avoiding investment in doomed drugs is poor solubility an industry wide problem?
-
April, 17-19
-
Lipinski C.A. Avoiding investment in doomed drugs is poor solubility an industry wide problem? Curr. Drug Discov. 2001;. April, 17-19.
-
(2001)
Curr. Drug Discov.
-
-
Lipinski, C.A.1
-
29
-
-
0035153841
-
Chem-tox informatics: Data mining using a medicinal chemistry block approach
-
Johnson D.E., et al. Chem-tox informatics: data mining using a medicinal chemistry block approach. Curr. Opin. Drug. Discov. Dev. 4:2001;1.
-
(2001)
Curr. Opin. Drug. Discov. Dev.
, vol.4
, pp. 1
-
-
Johnson, D.E.1
-
30
-
-
0034962557
-
Pharmacophore and three dimensional quantitative structure activity relationship methods for modeling cytochrome P450 active sites
-
Ekins S., et al. Pharmacophore and three dimensional quantitative structure activity relationship methods for modeling cytochrome P450 active sites. Drug Metab. Dispos. 29:2001;936-944.
-
(2001)
Drug Metab. Dispos.
, vol.29
, pp. 936-944
-
-
Ekins, S.1
-
31
-
-
0033011395
-
Three dimensional-quantitative structure activity relationship (3D-QSAR) analyses of inhibitors for CYP3A4
-
Ekins S., et al. Three dimensional-quantitative structure activity relationship (3D-QSAR) analyses of inhibitors for CYP3A4. J. Pharmacol. Exp. Ther. 290:1999;429-438.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 429-438
-
-
Ekins, S.1
-
32
-
-
0034950245
-
Development of a generalized, quantitative physicochemical model of CYP3A4 inhibition for use in early drug discovery
-
Riley R.J., et al. development of a generalized, quantitative physicochemical model of CYP3A4 inhibition for use in early drug discovery. Pharm. Res. 18:2001;652-655.
-
(2001)
Pharm. Res.
, vol.18
, pp. 652-655
-
-
Riley, R.J.1
-
33
-
-
0037204549
-
Pharmacophore modeling of cytochromes P450
-
de Groot M.J., Ekins S. Pharmacophore modeling of cytochromes P450. Adv. Drug Deliv. Rev. 54:2002;367-383.
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 367-383
-
-
De Groot, M.J.1
Ekins, S.2
-
34
-
-
0348209228
-
Role of CYP3A5 and CYP3A7 in drug-drug interactions
-
Stresser D.M., et al. Role of CYP3A5 and CYP3A7 in drug-drug interactions. Drug Metab. Rev. 33:(Suppl. 1):2001;134.
-
(2001)
Drug Metab. Rev.
, vol.33
, Issue.SUPPL. 1
, pp. 134
-
-
Stresser, D.M.1
-
35
-
-
0036320872
-
Comparative metabolic capabilities of CYP3A4, CYP3A5, and CYP3A7
-
Williams J.A., et al. Comparative metabolic capabilities of CYP3A4, CYP3A5, and CYP3A7. Drug Metab. Dispos. 30:2002;883-891.
-
(2002)
Drug Metab. Dispos.
, vol.30
, pp. 883-891
-
-
Williams, J.A.1
-
37
-
-
0000227103
-
Identification of three key residues in substrate recognition site 5 of human cytochrome P450 3A4 by cassette and site-directed mutagenesis
-
He Y.A., et al. Identification of three key residues in substrate recognition site 5 of human cytochrome P450 3A4 by cassette and site-directed mutagenesis. Biochemistry. 36:1997;8831-8839.
-
(1997)
Biochemistry
, vol.36
, pp. 8831-8839
-
-
He, Y.A.1
-
38
-
-
0031041652
-
Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P4503A4
-
Harlow G.R., Halpert J.R. Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P4503A4. J. Biol. Chem. 272:1997;5396-5402.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 5396-5402
-
-
Harlow, G.R.1
Halpert, J.R.2
-
39
-
-
0034108229
-
Dual role of human cytochrome P450 3A4 residue Phe-304 in substrate specificity and cooperativity
-
Domanski T.L., et al. Dual role of human cytochrome P450 3A4 residue Phe-304 in substrate specificity and cooperativity. J. Pharmacol. Exp. Ther. 293:2000;585-591.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.293
, pp. 585-591
-
-
Domanski, T.L.1
-
41
-
-
0034786492
-
Evidence of impaired cisapride metabolism in neonates
-
Treluyer J.-M., et al. Evidence of impaired cisapride metabolism in neonates. Br. J. Clin. Pharmacol. 52:2001;419-425.
-
(2001)
Br. J. Clin. Pharmacol.
, vol.52
, pp. 419-425
-
-
Treluyer, J.-M.1
-
42
-
-
0023200455
-
P-450 HFLa, a form of cytochrome P-450 purified from human fetal livers, is the 16 alpha-hydroxylase of dehydroepiandrosterone 3-sulfate
-
Kitada M., et al. P-450 HFLa, a form of cytochrome P-450 purified from human fetal livers, is the 16 alpha-hydroxylase of dehydroepiandrosterone 3-sulfate. J. Biol. Chem. 262:1987;13534-13537.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 13534-13537
-
-
Kitada, M.1
-
43
-
-
0028234586
-
Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily
-
Gorski J.C., et al. Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamily. Biochem. Pharmacol. 47:1994;1643-1653.
-
(1994)
Biochem. Pharmacol.
, vol.47
, pp. 1643-1653
-
-
Gorski, J.C.1
-
44
-
-
0033835442
-
Catalysis of the 4-hydroxylation of retinoic acids by CYP3A7 in human fetal hepatic tissues
-
Chen H., et al. Catalysis of the 4-hydroxylation of retinoic acids by CYP3A7 in human fetal hepatic tissues. Drug Metab. Dispos. 28:2000;1051-1057.
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 1051-1057
-
-
Chen, H.1
-
45
-
-
0002820079
-
Crystal structure of a human cytochrome P450 enzyme
-
Jhoti H., et al. Crystal structure of a human cytochrome P450 enzyme. Drug Metab. Rev. 34:(Suppl. 1):2002;10.
-
(2002)
Drug Metab. Rev.
, vol.34
, Issue.SUPPL. 1
, pp. 10
-
-
Jhoti, H.1
|