-
1
-
-
0033755482
-
Drug-drug interactions in medical patients: Effects of in-hospital treatment and relation to multiple drug use
-
Kohler, G.I.; Bode-Boger, S.M.; Busse, R.; Hoopmann, M.; Welte T; Boger, R.H. Drug-drug interactions in medical patients: effects of in-hospital treatment and relation to multiple drug use. Intern. J. of Clin. Pharma. Therap. 2000, 38(11), 504-13.
-
(2000)
Intern. J. of Clin. Pharma. Therap
, vol.38
, Issue.11
, pp. 504-513
-
-
Kohler, G.I.1
Bode-Boger, S.M.2
Busse, R.3
Hoopmann, M.4
Welte, T.5
Boger, R.H.6
-
2
-
-
34548805504
-
Mechanism-based inactivation of cytochrome P450 enzymes: Chemical mechanisms, structure-activity relationships and relationship to clinical drugdrug interactions and idiosyncratic adverse drug reactions
-
Kalgutkar, A.S.; Obach, R. S.; Maurer, T.S. Mechanism-based inactivation of cytochrome P450 enzymes: chemical mechanisms, structure-activity relationships and relationship to clinical drugdrug interactions and idiosyncratic adverse drug reactions. Curr. Drug Metab. 2007, 8(5), 407-447.
-
(2007)
Curr. Drug Metab
, vol.8
, Issue.5
, pp. 407-447
-
-
Kalgutkar, A.S.1
Obach, R.S.2
Maurer, T.S.3
-
3
-
-
61649128021
-
Validation of cytochrome P450 timedependent inhibition assays: A two-time point IC50 shift approach facilitates kinact assay design
-
Perloff, E. S; Mason, A. K; Dehal, S. S; Blanchard, A. P; Morgan, L.; Ho, T.; Dandeneau, A.; Crocker, R.M.; Chandler, C.M.; Boily, N.; Crespi, C.L.; Stresser, D. M. Validation of cytochrome P450 timedependent inhibition assays: a two-time point IC50 shift approach facilitates kinact assay design. Xenobiotica 2009, 39(2), 99-112.
-
(2009)
Xenobiotica
, vol.39
, Issue.2
, pp. 99-112
-
-
Perloff, E.S.1
Mason, A.K.2
Dehal, S.S.3
Blanchard, A.P.4
Morgan, L.5
Ho, T.6
Dandeneau, A.7
Crocker, R.M.8
Chandler, C.M.9
Boily, N.10
Crespi, C.L.11
Stresser, D.M.12
-
4
-
-
34250368905
-
Time-dependent CYP inhibition
-
Riley, R. J.; Grime, K.; Weaver, R. Time-dependent CYP inhibition. Expert Opin. Drug Metab. & Toxicol. 2007, 3(1), 51-66.
-
(2007)
Expert Opin. Drug Metab. & Toxicol
, vol.3
, Issue.1
, pp. 51-66
-
-
Riley, R.J.1
Grime, K.2
Weaver, R.3
-
5
-
-
0035523337
-
Metabolism profiling, and cytochrome P450 inhibition & induction in drug discovery
-
Yan, Z.; Caldwell, G. W. Metabolism profiling, and cytochrome P450 inhibition & induction in drug discovery. Curr. Top. Med. Chem. 2001, 1(5), 403-425.
-
(2001)
Curr. Top. Med. Chem
, vol.1
, Issue.5
, pp. 403-425
-
-
Yan, Z.1
Caldwell, G.W.2
-
6
-
-
0036226707
-
Characteristics and common properties of inhibitors, inducers, and activators of CYP [cytochrome P 450] enzymes
-
Hollenberg, P.F. Characteristics and common properties of inhibitors, inducers, and activators of CYP [cytochrome P 450] enzymes. Drug Metab. Rev. 2002, 34(1 & 2), 17-35.
-
(2002)
Drug Metab. Rev
, vol.34
, Issue.1-2
, pp. 17-35
-
-
Hollenberg, P.F.1
-
7
-
-
30744432123
-
Screening for reactive intermediates and toxicity assessment in drug discovery
-
Caldwell, G.W., Yan, Z. Screening for reactive intermediates and toxicity assessment in drug discovery Curr. Opin. Drug Disc. Develop. 2006, 9, 47-60.
-
(2006)
Curr. Opin. Drug Disc. Develop
, vol.9
, pp. 47-60
-
-
Caldwell, G.W.1
Yan, Z.2
-
8
-
-
0036825366
-
Rapidly distinguishing reversible and irreversible CYP450 inhibitors by using fluorometric kinetic analyses
-
Yan, Z.; Rafferty, B.; Caldwell, G.W.; Masucci, J. A. Rapidly distinguishing reversible and irreversible CYP450 inhibitors by using fluorometric kinetic analyses. Europ. J. Drug Metab. Pharmacok. 2002, 27(4), 281-287.
-
(2002)
Europ. J. Drug Metab. Pharmacok
, vol.27
, Issue.4
, pp. 281-287
-
-
Yan, Z.1
Rafferty, B.2
Caldwell, G.W.3
Masucci, J.A.4
-
9
-
-
7444242763
-
Utility of microtiter plate assays for human cytochrome P450 inhibition studies in drug discovery: Application of simple method for detecting quasi-irreversible and irreversible inhibitors
-
Naritomi, Y.; Teramura, Y.; Terashita, Shigeyuki; Kagayama, Akira. Utility of microtiter plate assays for human cytochrome P450 inhibition studies in drug discovery: application of simple method for detecting quasi-irreversible and irreversible inhibitors. Drug Metab. Pharmacok. 2004, 19(1), 55-61.
-
(2004)
Drug Metab. Pharmacok
, vol.19
, Issue.1
, pp. 55-61
-
-
Naritomi, Y.1
Teramura, Y.2
Terashita, S.3
Kagayama, A.4
-
10
-
-
33645980647
-
A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation
-
Ghanbari, F.; Rowland-Yeo, K.; Bloomer, J. C.; Clarke, S. E.; Lennard, M. S.; Tucker, G. T.; Rostami-Hodjegan, A. A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation. Curr. Drug Metab. 2006, 7(3), 315-334.
-
(2006)
Curr. Drug Metab
, vol.7
, Issue.3
, pp. 315-334
-
-
Ghanbari, F.1
Rowland-Yeo, K.2
Bloomer, J.C.3
Clarke, S.E.4
Lennard, M.S.5
Tucker, G.T.6
Rostami-Hodjegan, A.7
-
11
-
-
22944469767
-
Automated screening with confirmation of mechanismbased inactivation of CYP3A4, CYP2C9, CYP2C19, CYP2D6, and CYP1A2 in pooled human liver microsomes
-
Lim, H-K; Duczak, N. Jr.; Brougham, L.; Elliot, M.; Patel, K.; Chan, K. Automated screening with confirmation of mechanismbased inactivation of CYP3A4, CYP2C9, CYP2C19, CYP2D6, and CYP1A2 in pooled human liver microsomes. Drug Metab. Dispos. 2005, 33(8), 1211-1219.
-
(2005)
Drug Metab. Dispos
, vol.33
, Issue.8
, pp. 1211-1219
-
-
Lim, H-K.1
Duczak Jr., N.2
Brougham, L.3
Elliot, M.4
Patel, K.5
Chan, K.6
-
12
-
-
69249220270
-
Cocktail-substrate assay system for mechanism-based inhibition of CYP2C9, CYP2D6, and CYP3A using human liver microsomes at an early stage of drug development
-
Mori, K.; Hashimoto, H.; Takatsu, H.; Tsuda-Tsukimoto, M.; Kume, T. Cocktail-substrate assay system for mechanism-based inhibition of CYP2C9, CYP2D6, and CYP3A using human liver microsomes at an early stage of drug development. Xenobiotica 2009, 39(6), 415-422.
-
(2009)
Xenobiotica
, vol.39
, Issue.6
, pp. 415-422
-
-
Mori, K.1
Hashimoto, H.2
Takatsu, H.3
Tsuda-Tsukimoto, M.4
Kume, T.5
-
13
-
-
40949119511
-
An examination of IC50 and IC50-shift experiments in assessing time-dependent inhibition of CYP3A4, CYP2D6 and CYP2C9 in human liver microsomes
-
Berry, L.M.; Zhao, Z. An examination of IC50 and IC50-shift experiments in assessing time-dependent inhibition of CYP3A4, CYP2D6 and CYP2C9 in human liver microsomes. Drug Metab. Lett. 2008, 2(1), 51-59.
-
(2008)
Drug Metab. Lett
, vol.2
, Issue.1
, pp. 51-59
-
-
Berry, L.M.1
Zhao, Z.2
-
14
-
-
77955117355
-
Use of stable isotope labeled probes to facilitate liquid chromatography/mass spectrometry based high-throughput screening of time-dependent CYP inhibitors
-
Dasgupta, M.; Tang, W.; Caldwell, G.W.; Yan, Z. Use of stable isotope labeled probes to facilitate liquid chromatography/mass spectrometry based high-throughput screening of time-dependent CYP inhibitors. Rapid Comm. Mass Spectr. 2010, 24(15), 2177-2185.
-
(2010)
Rapid Comm. Mass Spectr
, vol.24
, Issue.15
, pp. 2177-2185
-
-
Dasgupta, M.1
Tang, W.2
Caldwell, G.W.3
Yan, Z.4
-
15
-
-
0028930481
-
Mechanism-based enzyme inactivators
-
Enzyme Kinetics and Mechanism, Part D
-
Silverman, R. B. Mechanism-based enzyme inactivators. Methods in Enzymology 1995, 249 (Enzyme Kinetics and Mechanism, Part D), 240-283.
-
(1995)
Methods in Enzymology
, vol.249
, pp. 240-283
-
-
Silverman, R.B.1
-
16
-
-
67649389519
-
The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: A perspective of the Pharmaceutical Research and Manufacturers of America
-
Grimm, S.W.; Einolf, H.J.; Hall, S.D.; He, K.; Lim, H-K; Ling, K.-H. J.; Lu, C.; Nomeir, A. A.; Seibert, E.; Skordos, K.W.; Tonn, G. R.; Van Horn, R.; Wang, R.W.; Wong, Y. N.; Yang, T. J.; Obach, R. S. The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: a perspective of the Pharmaceutical Research and Manufacturers of America. Drug Metab. Dispos. 2009, 37(7), 1355-1370
-
(2009)
Drug Metab. Dispos
, vol.37
, Issue.7
, pp. 1355-1370
-
-
Grimm, S.W.1
Einolf, H.J.2
Hall, S.D.3
He, K.4
Lim, H-K.5
Ling, K.-H.J.6
Lu, C.7
Nomeir, A.A.8
Seibert, E.9
Skordos, K.W.10
Tonn, G.R.11
van Horn, R.12
Wang, R.W.13
Wong, Y.N.14
Yang, T.J.15
Obach, R.S.16
-
17
-
-
0033831197
-
An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation
-
Mayhew, B.S.; Jones, D.R.; Hall, S.D. An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation. Drug Metab. Dispos. 2000, 28(9), 1031-1037.
-
(2000)
Drug Metab. Dispos
, vol.28
, Issue.9
, pp. 1031-1037
-
-
Mayhew, B.S.1
Jones, D.R.2
Hall, S.D.3
-
18
-
-
80054734196
-
Utilizing drug-drug interaction prediction tools during drug development: Enhanced decision making based on clinical risk
-
Shardlow, C.E.; Generaux, G.T.; MacLauchlin, C.C.; Pons, N.; Skordos, K.W.; Bloomer, J.C. Utilizing drug-drug interaction prediction tools during drug development: enhanced decision making based on clinical risk. Drug Metab. Dispos. 2011, 39(11), 2076-2084.
-
(2011)
Drug Metab. Dispos
, vol.39
, Issue.11
, pp. 2076-2084
-
-
Shardlow, C.E.1
Generaux, G.T.2
McLauchlin, C.C.3
Pons, N.4
Skordos, K.W.5
Bloomer, J.C.6
-
19
-
-
80053499643
-
Prediction of drug-drug interactions arising from mechanism-based inactivation: Key input parameters and impact on risk assessment
-
Wong, S. G. Prediction of drug-drug interactions arising from mechanism-based inactivation: key input parameters and impact on risk assessment. Curr. Drug Metab. 2011, 12(9), 871-890.
-
(2011)
Curr. Drug Metab
, vol.12
, Issue.9
, pp. 871-890
-
-
Wong, S.G.1
-
20
-
-
27644596457
-
Predicting in vivo drug interactions from in vitro drug discovery data
-
Wienkers, L.C.; Heath, T. G. Predicting in vivo drug interactions from in vitro drug discovery data. Nature Reviews Drug Disc. 2005, 4(10), 825-833.
-
(2005)
Nature Reviews Drug Disc
, vol.4
, Issue.10
, pp. 825-833
-
-
Wienkers, L.C.1
Heath, T.G.2
-
21
-
-
29244447987
-
The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions
-
Obach, R. S.; Walsky, R. L.; Venkatakrishnan, K.; Gaman, E. A.; Houston, J. B.; Tremaine, L. M. The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions. J. Pharm. Experim. Therap. 2006, 316(1), 336-348.
-
(2006)
J. Pharm. Experim. Therap
, vol.316
, Issue.1
, pp. 336-348
-
-
Obach, R.S.1
Walsky, R.L.2
Venkatakrishnan, K.3
Gaman, E.A.4
Houston, J.B.5
Tremaine, L.M.6
-
22
-
-
33846449874
-
Mechanismbased inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions
-
Obach, R. S.; Walsky, R. L.; Venkatakrishnan, K. Mechanismbased inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions. Drug Metab. Dispos. 2007, 35(2), 246-255.
-
(2007)
Drug Metab. Dispos
, vol.35
, Issue.2
, pp. 246-255
-
-
Obach, R.S.1
Walsky, R.L.2
Venkatakrishnan, K.3
-
23
-
-
49649116162
-
Potential role of intestinal first-pass metabolism in the prediction of drug-drug interactions
-
Galetin, A.; Gertz, M.; Houston, J. B. Potential role of intestinal first-pass metabolism in the prediction of drug-drug interactions. Expert Opinion on Drug Metab. & Toxicol. 2008, 4(7), 909-922.
-
(2008)
Expert Opinion on Drug Metab. & Toxicol
, vol.4
, Issue.7
, pp. 909-922
-
-
Galetin, A.1
Gertz, M.2
Houston, J.B.3
-
24
-
-
79957493995
-
Prediction of time-dependent CYP3A4 drug-drug interactions by physiologically based pharmacokinetic modelling: Impact of inactivation parameters and enzyme turnover
-
Yeo, K. R.; Walsky, R.L.; Jamei, M.; Rostami-Hodjegan, A.; Tucker, G. T. Prediction of time-dependent CYP3A4 drug-drug interactions by physiologically based pharmacokinetic modelling: Impact of inactivation parameters and enzyme turnover. Europ. J. Pharma. Sci. 2011, 43(3), 160-173.
-
(2011)
Europ. J. Pharma. Sci
, vol.43
, Issue.3
, pp. 160-173
-
-
Yeo, K.R.1
Walsky, R.L.2
Jamei, M.3
Rostami-Hodjegan, A.4
Tucker, G.T.5
-
25
-
-
67649131017
-
The Simcyp population-based ADME simulator
-
Jamei, M.; Marciniak, S.; Feng, K.; Barnett, A.; Tucker, G.; Rostami-Hodjegan, A. The Simcyp population-based ADME simulator. Expert Opinion Drug Metab. & Toxicol. 2009, 5(2), 211-223.
-
(2009)
Expert Opinion Drug Metab. & Toxicol
, vol.5
, Issue.2
, pp. 211-223
-
-
Jamei, M.1
Marciniak, S.2
Feng, K.3
Barnett, A.4
Tucker, G.5
Rostami-Hodjegan, A.6
-
26
-
-
77953787344
-
Confidence assessment of the simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors
-
Wang, Y-H. Confidence assessment of the simcyp time-based approach and a static mathematical model in predicting clinical drug-drug interactions for mechanism-based CYP3A inhibitors. Drug Metab. Dispos. 2010, 38(7),1094-1104.
-
(2010)
Drug Metab. Dispos
, vol.38
, Issue.7
, pp. 1094-1104
-
-
Wang, Y.-H.1
-
27
-
-
35648968125
-
Comparison of different approaches to predict metabolic drug-drug interactions
-
Einolf, H. J. Comparison of different approaches to predict metabolic drug-drug interactions. Xenobiotica 2007, 37(10/11), 1257-1294.
-
(2007)
Xenobiotica
, vol.37
, Issue.10-11
, pp. 1257-1294
-
-
Einolf, H.J.1
-
28
-
-
24644441043
-
Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol
-
Yang, J.; Jamei, M.; Yeo, K. R.; Tucker, G.T.; Rostami-Hodjegan, A. Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol. Europ. J. Pharma. Sci. 2005, 26(3-4), 334-340.
-
(2005)
Europ. J. Pharma. Sci
, vol.26
, Issue.3-4
, pp. 334-340
-
-
Yang, J.1
Jamei, M.2
Yeo, K.R.3
Tucker, G.T.4
Rostami-Hodjegan, A.5
-
29
-
-
33750357086
-
The impact of experimental design on assessing mechanism-based inactivation of CYP2D6 by MDMA (Ecstasy)
-
Van, L.M.; Heydari, A.; Yang, J.; Hargreaves, J.; Yeo, K. R.K.; Lennard, M.S.; Tucker, G.T.; Rostami-Hodjegan, A. The impact of experimental design on assessing mechanism-based inactivation of CYP2D6 by MDMA (Ecstasy). J. Psychopharma. 2006, 20(6), 834-841.
-
(2006)
J. Psychopharma
, vol.20
, Issue.6
, pp. 834-841
-
-
Van, L.M.1
Heydari, A.2
Yang, J.3
Hargreaves, J.4
Yeo, K.R.K.5
Lennard, M.S.6
Tucker, G.T.7
Rostami-Hodjegan, A.8
-
30
-
-
79960594081
-
An evaluation of the dilution method for identifying metabolismdependent inhibitors of cytochrome P450 enzymes
-
Parkinson, A.; Kazmi, F.; Buckley, D. B.; Yerino, P.; Paris, B. L.; Holsapple, J.; Toren, P.; Otradovec, S.M.; Ogilvie, B. W. An evaluation of the dilution method for identifying metabolismdependent inhibitors of cytochrome P450 enzymes. Drug Metab. Dispos. 2011, 39(8), 1370-1387.
-
(2011)
Drug Metab. Dispos
, vol.39
, Issue.8
, pp. 1370-1387
-
-
Parkinson, A.1
Kazmi, F.2
Buckley, D.B.3
Yerino, P.4
Paris, B.L.5
Holsapple, J.6
Toren, P.7
Otradovec, S.M.8
Ogilvie, B.W.9
-
31
-
-
0036891924
-
Microsomal protein concentration modifies the apparent inhibitory potency of CYP3A inhibitors
-
Tran, T.H.; Von Moltke, L. L.; Venkatakrishnan, K.; Granda, B.W.; Gibbs, M.A.; Obach, R. S.; Harmatz, J.S.; Greenblatt, D.J. Microsomal protein concentration modifies the apparent inhibitory potency of CYP3A inhibitors. Drug Metab. Dispos. 2002, 30(12), 1441-1445.
-
(2002)
Drug Metab. Dispos
, vol.30
, Issue.12
, pp. 1441-1445
-
-
Tran, T.H.1
von Moltke, L.L.2
Venkatakrishnan, K.3
Granda, B.W.4
Gibbs, M.A.5
Obach, R.S.6
Harmatz, J.S.7
Greenblatt, D.J.8
-
32
-
-
33750547308
-
CYP2C9 inhibition: Impact of probe selection and pharmacogenetics on in vitro inhibition profiles
-
Kumar, V.; Wahlstrom, J.L.; Rock, D.A.; Warren, C.J.; Gorman, L.A.; Tracy, T.S. CYP2C9 inhibition: impact of probe selection and pharmacogenetics on in vitro inhibition profiles. Drug Metab. Dispos. 2006, 34(12), 1966-1975.
-
(2006)
Drug Metab. Dispos
, vol.34
, Issue.12
, pp. 1966-1975
-
-
Kumar, V.1
Wahlstrom, J.L.2
Rock, D.A.3
Warren, C.J.4
Gorman, L.A.5
Tracy, T.S.6
-
33
-
-
33645980647
-
A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation
-
Ghanbari, F.; Rowland-Yeo, K.; Bloomer, J. C.; Clarke, S. E.; Lennard, M. S.; Tucker, G. T.; Rostami-Hodjegan, A. A critical evaluation of the experimental design of studies of mechanism based enzyme inhibition, with implications for in vitro-in vivo extrapolation. Curr. Drug Metab. 2006, 7(3), 315-334.
-
(2006)
Curr. Drug Metab
, vol.7
, Issue.3
, pp. 315-334
-
-
Ghanbari, F.1
Rowland-Yeo, K.2
Bloomer, J.C.3
Clarke, S.E.4
Lennard, M.S.5
Tucker, G.T.6
Rostami-Hodjegan, A.7
-
34
-
-
34548738229
-
Drug-drug interactions via mechanism-based cytochrome P450 inactivation: Points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation
-
Venkatakrishnan, K.; Obach, R. S. Drug-drug interactions via mechanism-based cytochrome P450 inactivation: points to consider for risk assessment from in vitro data and clinical pharmacologic evaluation. Curr. Drug Metab. 2007, 8(5), 449-462.
-
(2007)
Curr. Drug Metab
, vol.8
, Issue.5
, pp. 449-462
-
-
Venkatakrishnan, K.1
Obach, R.S.2
-
35
-
-
35548948469
-
Use of isolated hepatocyte preparations for cytochrome P450 inhibition studies: Comparison with microsomes for Ki determination
-
Brown, H.S.; Chadwick, A.; Houston, J.B. Use of isolated hepatocyte preparations for cytochrome P450 inhibition studies: comparison with microsomes for Ki determination. Drug Metab. Dispos. 2007, 35(11), 2119-2126.
-
(2007)
Drug Metab. Dispos
, vol.35
, Issue.11
, pp. 2119-2126
-
-
Brown, H.S.1
Chadwick, A.2
Houston, J.B.3
-
36
-
-
80054733298
-
Determination of time-dependent inactivation of CYP3A4 in cryopreserved human hepatocytes and assessment of human drug-drug interactions
-
Chen, Y.; Liu, L.; Monshouwer, M.; Fretland, A.J. Determination of time-dependent inactivation of CYP3A4 in cryopreserved human hepatocytes and assessment of human drug-drug interactions. Drug Metab. Dispos. 2011, 39(11), 2085-2092.
-
(2011)
Drug Metab. Dispos
, vol.39
, Issue.11
, pp. 2085-2092
-
-
Chen, Y.1
Liu, L.2
Monshouwer, M.3
Fretland, A.J.4
-
37
-
-
71049127036
-
Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator
-
Xu, L.; Chen, Y.; Pan, Y.; Skiles, G.L.; Shou, M. Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator. Drug Metab. Dispos. 2009, 37(12), 2330-2339.
-
(2009)
Drug Metab. Dispos
, vol.37
, Issue.12
, pp. 2330-2339
-
-
Xu, L.1
Chen, Y.2
Pan, Y.3
Skiles, G.L.4
Shou, M.5
-
38
-
-
0031696409
-
The contribution of intestinal and hepatic CYP 3A to the interaction between midazolam and clarithromycin
-
(St. Louis)
-
Gorski, J.C.; Jones, D.R.; Haehner-Daniels, B.D.; Hamman, M.A.; O'Mara, E.M.; Hall, S.D. The contribution of intestinal and hepatic CYP 3A to the interaction between midazolam and clarithromycin. Clin. Pharma. Therap. (St. Louis), 1998, 64(2), 133-143.
-
(1998)
Clin. Pharma. Therap
, vol.64
, Issue.2
, pp. 133-143
-
-
Gorski, J.C.1
Jones, D.R.2
Haehner-Daniels, B.D.3
Hamman, M.A.4
O'Mara, E.M.5
Hall, S.D.6
-
39
-
-
47749122616
-
Cytochrome P450 turnover: Regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions
-
Yang, J.; Liao, M.; Shou, M.; Jamei, M.; Yeo, K. R.; Tucker, G.T.; Rostami-Hodjegan, A. Cytochrome P450 turnover: regulation of synthesis and degradation, methods for determining rates, and implications for the prediction of drug interactions. Curr. Drug Metab. 2008, 9(5), 384-393.
-
(2008)
Curr. Drug Metab
, vol.9
, Issue.5
, pp. 384-393
-
-
Yang, J.1
Liao, M.2
Shou, M.3
Jamei, M.4
Yeo, K.R.5
Tucker, G.T.6
Rostami-Hodjegan, A.7
-
40
-
-
0042533918
-
The interaction of diltiazem with simvastatin
-
(St. Louis)
-
Mousa, O.; Brater, D. C.; Sundblad, K. J.; Hall, S. D. The interaction of diltiazem with simvastatin. Clin. Pharma. Therap. (St. Louis), 2000, 67(3), 267-274.
-
(2000)
Clin. Pharma. Therap
, vol.67
, Issue.3
, pp. 267-274
-
-
Mousa, O.1
Brater, D.C.2
Sundblad, K.J.3
Hall, S.D.4
-
41
-
-
24944510505
-
Cytochrome P 450 enzymes mechanism based inhibitors: Common sub-structures and reactivity
-
Fontana, E.; Dansette, P. M.; Poli, S. M. Cytochrome P 450 enzymes mechanism based inhibitors: Common sub-structures and reactivity. Curr. Drug Metab. 2005, 6(5), 413-454.
-
(2005)
Curr. Drug Metab
, vol.6
, Issue.5
, pp. 413-454
-
-
Fontana, E.1
Dansette, P.M.2
Poli, S.M.3
|