-
1
-
-
67349165556
-
Understanding nuclear receptors using computational methods
-
Ai, N., Krasowski, M. D., Welsh, W. J., Ekins, S. (2009). Understanding nuclear receptors using computational methods. Drug Discov Today 14: 486-494.
-
(2009)
Drug Discov Today
, vol.14
, pp. 486-494
-
-
Ai, N.1
Krasowski, M.D.2
Welsh, W.J.3
Ekins, S.4
-
2
-
-
13144260727
-
Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction
-
DOI 10.1073/pnas.95.21.12208
-
Bertilsson, G., Heidrich, J., Svensson, K., Asman, M., Jendeberg, L., Sydow-Backman, M., et al. (1998). Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction. Proc Natl Acad Sci USA 95: 12208-12213. (Pubitemid 28483744)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.21
, pp. 12208-12213
-
-
Bertilsson, G.1
Heidrich, J.2
Svensson, K.3
Asman, M.4
Jendeberg, L.5
Sydow-Backman, M.6
Ohlsson, R.7
Postlind, H.8
Blomquist, P.9
Berkenstam, A.10
-
3
-
-
0018838326
-
Autoinduction of carbamazepine metabolism in children examined by a stable isotope technique
-
Bertilsson, L., Hojer, B., Tybring, G., Osterloh, J., Rane, A. (1980). Autoinduction of carbamazepine metabolism in children examined by a stable isotope technique. Clin Pharmacol Ther 27: 83-88. (Pubitemid 10096585)
-
(1980)
Clinical Pharmacology and Therapeutics
, vol.27
, Issue.1
, pp. 83-88
-
-
Bertilsson, L.1
Hojer, B.2
Tybring, G.3
-
4
-
-
0032532721
-
Orphan nuclear receptors - New ligands and new possibilities
-
Blumberg, B., Evans, R. M. (1998). Orphan nuclear receptors-new ligands and new possibilities. Genes Dev 12: 3149-3155. (Pubitemid 28496259)
-
(1998)
Genes and Development
, vol.12
, Issue.20
, pp. 3149-3155
-
-
Blumberg, B.1
Evans, R.M.2
-
5
-
-
23144467497
-
Structure and function of the human nuclear xenobiotic receptor PXR
-
DOI 10.2174/1389200054633844
-
Carnahan, V. E., Redinbo, M. R. (2005). Structure and function of the human nuclear xenobiotic receptor PXR. Curr Drug Metab 6: 357-367. (Pubitemid 41086768)
-
(2005)
Current Drug Metabolism
, vol.6
, Issue.4
, pp. 357-367
-
-
Carnahan, V.E.1
Redinbo, M.R.2
-
6
-
-
67649404709
-
In vitro and in vivo induction of cytochrome p450: A survey of the current practices and recommendations: A pharmaceutical research and manufacturers of america perspective
-
Chu, V., Einolf, H. J., Evers, R., Kumar, G., Moore, D., Ripp, S., et al. (2009). In vitro and in vivo induction of cytochrome p450: a survey of the current practices and recommendations: a pharmaceutical research and manufacturers of america perspective. Drug Metab Dispos 37: 1339-1354.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1339-1354
-
-
Chu, V.1
Einolf, H.J.2
Evers, R.3
Kumar, G.4
Moore, D.5
Ripp, S.6
-
7
-
-
49149108728
-
Application and interpretation of hPXR screening data: Validation of reporter signal requirements for prediction of clinically relevant CYP3A4 inducers
-
Cui, X., Thomas, A., Gerlach, V., White, R. E., Morrison, R. A., Cheng, K. C. (2008). Application and interpretation of hPXR screening data: validation of reporter signal requirements for prediction of clinically relevant CYP3A4 inducers. Biochem Pharmacol 76: 680-689.
-
(2008)
Biochem Pharmacol
, vol.76
, pp. 680-689
-
-
Cui, X.1
Thomas, A.2
Gerlach, V.3
White, R.E.4
Morrison, R.A.5
Cheng, K.C.6
-
8
-
-
34548308480
-
Human pregnane X receptor antagonists and agonists define molecular requirements for different binding sites
-
DOI 10.1124/mol.107.038398
-
Ekins, S., Chang, C., Mani, S., Krasowski, M. D., Reschly, E. J., Iyer, M., et al. (2007). Human pregnane X receptor antagonists and agonists define molecular requirements for different binding sites. Mol Pharmacol 72: 592-603. (Pubitemid 47347294)
-
(2007)
Molecular Pharmacology
, vol.72
, Issue.3
, pp. 592-603
-
-
Ekins, S.1
Chang, C.2
Mani, S.3
Krasowski, M.D.4
Reschly, E.J.5
Iyer, M.6
Kholodovych, V.7
Ai, N.8
Welsh, W.J.9
Sinz, M.10
Swaan, P.W.11
Patel, R.12
Bachmann, K.13
-
9
-
-
0034781795
-
Use of a reporter gene assay to predict and rank the potency and efficacy of CYP3A4 inducers
-
El-Sankary, W., Gibson, G. G., Ayrton, A., Plant, N. (2001). Use of a reporter gene assay to predict and rank the potency and efficacy of CYP3A4 inducers. Drug Metab Dispos 29: 1499-1504. (Pubitemid 33000699)
-
(2001)
Drug Metabolism and Disposition
, vol.29
, Issue.11
, pp. 1499-1504
-
-
El-Sankary, W.1
Gibson, G.G.2
Ayrton, A.3
Plant, N.4
-
10
-
-
79955690629
-
-
EMA Guideline on the investigation of drug interactions Accessed on September XX 2012
-
EMA. (2012). Guideline on the investigation of drug interactions. Guideline on the investigation of drug interactions. Available at: http://www.ema.europa.eu/docs/en-GB/document-library/Scientific-guideline/2012/ 07/WC500129606.pdf. Accessed on September XX, 2012.
-
(2012)
Guideline on the Investigation of Drug Interactions
-
-
-
11
-
-
77953233959
-
Development of a UGT1A1 reporter gene assay for induction studies: Correlation between reporter gene data and regulation of UGT1A1 in human hepatocytes
-
Enoru-Eta, J., Yengi, L. G., He, X., Kubik, J., Kao, J., Scatina, J. (2010). Development of a UGT1A1 reporter gene assay for induction studies: correlation between reporter gene data and regulation of UGT1A1 in human hepatocytes. Drug Metab Lett 4: 31-38.
-
(2010)
Drug Metab Lett
, vol.4
, pp. 31-38
-
-
Enoru-Eta, J.1
Yengi, L.G.2
He, X.3
Kubik, J.4
Kao, J.5
Scatina, J.6
-
12
-
-
77958498196
-
Evaluation of models for predicting drug-drug interactions due to induction
-
Fahmi, O. A., Ripp, S. L. (2010). Evaluation of models for predicting drug-drug interactions due to induction. Expert Opin Drug Metab Toxicol 6: 1399-1416.
-
(2010)
Expert Opin Drug Metab Toxicol
, vol.6
, pp. 1399-1416
-
-
Fahmi, O.A.1
Ripp, S.L.2
-
13
-
-
84865415281
-
-
FDA Guidance for industry: drug interaction studies-study design, data analysis,implications for dosing, and labeling recommendations
-
FDA. (2012). Guidance for industry: drug interaction studies-study design, data analysis,implications for dosing, and labeling recommendations. Guidance for industry: drug interaction studies-study design, data analysis,implications for dosing, and labeling recommendations. Available at: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/ Guidances/UCM292362.pdf.
-
(2012)
Guidance for Industry: Drug Interaction Studies-study Design, Data Analysis,implications for Dosing, and Labeling Recommendations
-
-
-
14
-
-
58149087619
-
Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: Reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model
-
Fotsch, C., Bartberger, M. D., Bercot, E. A., Chen, M., Cupples, R., Emery, M., et al. (2008). Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model. J Med Chem 51: 7953-7967.
-
(2008)
J Med Chem
, vol.51
, pp. 7953-7967
-
-
Fotsch, C.1
Bartberger, M.D.2
Bercot, E.A.3
Chen, M.4
Cupples, R.5
Emery, M.6
-
15
-
-
33847056693
-
Attenuating pregnane X receptor (PXR) activation: A molecular modelling approach
-
Gao, Y. D., Olson, S. H., Balkovec, J. M., Zhu, Y., Royo, I., Yabut, J., et al. (2007). Attenuating pregnane X receptor (PXR) activation: a molecular modelling approach. Xenobiotica 37: 124-138.
-
(2007)
Xenobiotica
, vol.37
, pp. 124-138
-
-
Gao, Y.D.1
Olson, S.H.2
Balkovec, J.M.3
Zhu, Y.4
Royo, I.5
Yabut, J.6
-
16
-
-
33144459032
-
Cytochrome P450 and xenobiotic receptor humanized mice
-
DOI 10.1146/annurev.pharmtox.45.120403.100007
-
Gonzalez, F. J., Yu, A. M. (2006). Cytochrome P450 and xenobiotic receptor humanized mice. Annu Rev Pharmacol Toxicol 46: 41-64. (Pubitemid 43271183)
-
(2006)
Annual Review of Pharmacology and Toxicology
, vol.46
, pp. 41-64
-
-
Gonzalez, F.J.1
Yu, A.-M.2
-
17
-
-
44149104931
-
Comparison of immortalized Fa2N-4 cells and human hepatocytes as in vitro models for cytochrome P450 induction
-
DOI 10.1124/dmd.108.020677
-
Hariparsad, N., Carr, B. A., Evers, R., Chu, X. (2008). Comparison of immortalized Fa2N-4 cells and human hepatocytes as in vitro models for cytochrome P450 induction. Drug Metab Dispos 36: 1046-1055. (Pubitemid 351717461)
-
(2008)
Drug Metabolism and Disposition
, vol.36
, Issue.6
, pp. 1046-1055
-
-
Hariparsad, N.1
Carr, B.A.2
Evers, R.3
Chu, X.4
-
18
-
-
22244435560
-
Potent inhibitors of subgenomic hepatitis C virus RNA replication through optimization of indole-N-acetamide allosteric inhibitors of the viral NS5B polymerase
-
DOI 10.1021/jm050056+
-
Harper, S., Avolio, S., Pacini, B., Di Filippo, M., Altamura, S., Tomei, L., et al. (2005). Potent inhibitors of subgenomic hepatitis C virus RNA replication through optimization of indole-N-acetamide allosteric inhibitors of the viral NS5B polymerase. J Med Chem 48: 4547-4557. (Pubitemid 40993416)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.14
, pp. 4547-4557
-
-
Harper, S.1
Avolio, S.2
Pacini, B.3
Di Filippo, M.4
Altamura, S.5
Tomei, L.6
Paonessa, G.7
Di Marco, S.8
Carfi, A.9
Giuliano, C.10
Padron, J.11
Bonelli, F.12
Migliaccio, G.13
De Francesco, R.14
Laufer, R.15
Rowley, M.16
Narjes, F.17
-
19
-
-
80052011288
-
Quantitative prediction of human pregnane X receptor and cytochrome P450 3A4 mediated drug-drug interaction in a novel multiple humanized mouse line
-
Hasegawa, M., Kapelyukh, Y., Tahara, H., Seibler, J., Rode, A., Krueger, S., et al. (2011). Quantitative prediction of human pregnane X receptor and cytochrome P450 3A4 mediated drug-drug interaction in a novel multiple humanized mouse line. Mol Pharmacol 80: 518-528.
-
(2011)
Mol Pharmacol
, vol.80
, pp. 518-528
-
-
Hasegawa, M.1
Kapelyukh, Y.2
Tahara, H.3
Seibler, J.4
Rode, A.5
Krueger, S.6
-
20
-
-
34247505094
-
Induction of drug metabolizing enzymes: A survey of in vitro methodologies and interpretations used in the pharmaceutical industry-Do they comply with FDA recommendations?
-
DOI 10.1016/j.cbi.2006.12.009, PII S0009279706003619
-
Hewitt, N. J., De Kanter, R., Lecluyse, E. (2007). Induction of drug metabolizing enzymes: a survey of in vitro methodologies and interpretations used in the pharmaceutical industry-do they comply with FDA recommendations? Chem Biol Interact 168: 51-65. (Pubitemid 46659920)
-
(2007)
Chemico-Biological Interactions
, vol.168
, Issue.1
, pp. 51-65
-
-
Hewitt, N.J.1
De Kanter, R.2
LeCluyse, E.3
-
21
-
-
37549060373
-
Regulation of UDP-glucuronosyltransferase (UGT) 1A1 by progesterone and its impact on labetalol elimination
-
Jeong, H., Choi, S., Song, J. W., Chen, H., Fischer, J. H. (2008). Regulation of UDP-glucuronosyltransferase (UGT) 1A1 by progesterone and its impact on labetalol elimination. Xenobiotica 38: 62-75.
-
(2008)
Xenobiotica
, vol.38
, pp. 62-75
-
-
Jeong, H.1
Choi, S.2
Song, J.W.3
Chen, H.4
Fischer, J.H.5
-
22
-
-
17744375160
-
The pregnane X receptor: A promiscuous xenobiotic receptor that has diverged during evolution
-
DOI 10.1210/me.14.1.27
-
Jones, S. A., Moore, L. B., Shenk, J. L., Wisely, G. B., Hamilton, G. A., Mckee, D. D., et al. (2000). The pregnane X receptor: a promiscuous xenobiotic receptor that has diverged during evolution. Mol Endocrinol 14: 27-39. (Pubitemid 32260325)
-
(2000)
Molecular Endocrinology
, vol.14
, Issue.1
, pp. 27-39
-
-
Jones, S.A.1
Moore, L.B.2
Shenk, J.L.3
Wisely, G.B.4
Hamilton, G.A.5
McKee, D.D.6
Tomkinson, N.C.O.7
LeCluyse, E.L.8
Lambert, M.H.9
Willson, T.M.10
Kliewer, S.A.11
Moore, J.T.12
-
23
-
-
47949086965
-
Machine learning methods and docking for predicting human pregnane X receptor activation
-
Khandelwal, A., Krasowski, M. D., Reschly, E. J., Sinz, M. W., Swaan, P. W., Ekins, S. (2008). Machine learning methods and docking for predicting human pregnane X receptor activation. Chem Res Toxicol 21: 1457-1467.
-
(2008)
Chem Res Toxicol
, vol.21
, pp. 1457-1467
-
-
Khandelwal, A.1
Krasowski, M.D.2
Reschly, E.J.3
Sinz, M.W.4
Swaan, P.W.5
Ekins, S.6
-
24
-
-
73149087257
-
Evaluation of cynomolgus monkey pregnane X receptor, primary hepatocyte, and in vivo pharmacokinetic changes in predicting human CYP3A4 induction
-
Kim, S., Dinchuk, J. E., Anthony, M. N., Orcutt, T., Zoeckler, M. E., Sauer, M. B., et al. (2010). Evaluation of cynomolgus monkey pregnane X receptor, primary hepatocyte, and in vivo pharmacokinetic changes in predicting human CYP3A4 induction. Drug Metab Dispos 38: 16-24.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 16-24
-
-
Kim, S.1
Dinchuk, J.E.2
Anthony, M.N.3
Orcutt, T.4
Zoeckler, M.E.5
Sauer, M.B.6
-
25
-
-
53749106271
-
Quantitative relationship between rifampicin exposure and induction of Cyp3a11 in SXR humanized mice: Extrapolation to human CYP3A4 induction potential
-
Kim, S., Pray, D., Zheng, M., Morgan, D. G., Pizzano, J. G., Zoeckler, M. E., et al. (2008). Quantitative relationship between rifampicin exposure and induction of Cyp3a11 in SXR humanized mice: extrapolation to human CYP3A4 induction potential. Drug Metab Lett 2: 169-175.
-
(2008)
Drug Metab Lett
, vol.2
, pp. 169-175
-
-
Kim, S.1
Pray, D.2
Zheng, M.3
Morgan, D.G.4
Pizzano, J.G.5
Zoeckler, M.E.6
-
26
-
-
0036799870
-
The nuclear pregnane X receptor: A key regulator of xenobiotic metabolism
-
DOI 10.1210/er.2001-0038
-
Kliewer, S. A., Goodwin, B., Willson, T. M. (2002). The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism. Endocr Rev 23: 687-702. (Pubitemid 35191629)
-
(2002)
Endocrine Reviews
, vol.23
, Issue.5
, pp. 687-702
-
-
Kliewer, S.A.1
Goodwin, B.2
Willson, T.M.3
-
27
-
-
0032498303
-
An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway
-
DOI 10.1016/S0092-8674(00)80900-9
-
Kliewer, S. A., Moore, J. T., Wade, L., Staudinger, J. L., Watson, M. A., Jones, S. A., et al. (1998). An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway. Cell 92: 73-82. (Pubitemid 28053299)
-
(1998)
Cell
, vol.92
, Issue.1
, pp. 73-82
-
-
Kliewer, S.A.1
Moore, J.T.2
Wade, L.3
Staudinger, J.L.4
Watson, M.A.5
Jones, S.A.6
McKee, D.D.7
Oliver, B.B.8
Willson, T.M.9
Zetterstrom, R.H.10
Perlmann, T.11
Lehmann, J.M.12
-
28
-
-
34548350509
-
Discovery of a highly active ligand of human pregnane X receptor: A case study from pharmacophore modeling and virtual screening to "in vivo" biological activity
-
DOI 10.1124/mol.106.033415
-
Lemaire, G., Benod, C., Nahoum, V., Pillon, A., Boussioux, A. M., Guichou, J. F., et al. (2007). Discovery of a highly active ligand of human pregnane x receptor: a case study from pharmacophore modeling and virtual screening to "in vivo" biological activity. Mol Pharmacol 72: 572-581. (Pubitemid 47347292)
-
(2007)
Molecular Pharmacology
, vol.72
, Issue.3
, pp. 572-581
-
-
Lemaire, G.1
Benod, C.2
Nahoum, V.3
Pillon, A.4
Boussioux, A.-M.5
Guichou, J.-F.6
Subra, G.7
Pascussi, J.-M.8
Bourguet, W.9
Chavanieu, A.10
Balaguer, P.11
-
29
-
-
84863122056
-
An insulin-like growth factor 1 receptor inhibitor induces CYP3A4 expression through a pregnane X receptor-independent, noncanonical constitutive androstane receptor-related mechanism
-
Li, L., Sinz, M. W., Zimmermann, K., Wang, H. (2012). An insulin-like growth factor 1 receptor inhibitor induces CYP3A4 expression through a pregnane X receptor-independent, noncanonical constitutive androstane receptor-related mechanism. J Pharmacol Exp Ther 340: 688-697.
-
(2012)
J Pharmacol Exp Ther
, vol.340
, pp. 688-697
-
-
Li, L.1
Sinz, M.W.2
Zimmermann, K.3
Wang, H.4
-
30
-
-
84866249554
-
Development of in silico filters to predict activation of the pregnane X receptor (PXR) by structurally diverse drug-like molecules
-
Matter, H., Anger, L. T., Giegerich, C., Gussregen, S., Hessler, G., Baringhaus, K. H. (2012). Development of in silico filters to predict activation of the pregnane X receptor (PXR) by structurally diverse drug-like molecules. Bioorg Med Chem 20: 5352-5365.
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 5352-5365
-
-
Matter, H.1
Anger, L.T.2
Giegerich, C.3
Gussregen, S.4
Hessler, G.5
Baringhaus, K.H.6
-
31
-
-
66649089506
-
Evaluation of multiple in vitro systems for assessment of CYP3A4 induction in drug discovery: Human hepatocytes, pregnane X receptor reporter gene, and Fa2N-4 and HepaRG cells
-
Mcginnity, D. F., Zhang, G., Kenny, J. R., Hamilton, G. A., Otmani, S., Stams, K. R., et al. (2009). Evaluation of multiple in vitro systems for assessment of CYP3A4 induction in drug discovery: human hepatocytes, pregnane X receptor reporter gene, and Fa2N-4 and HepaRG cells. Drug Metab Dispos 37: 1259-1268.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1259-1268
-
-
McGinnity, D.F.1
Zhang, G.2
Kenny, J.R.3
Hamilton, G.A.4
Otmani, S.5
Stams, K.R.6
-
32
-
-
34548532926
-
Comparison of inducibility of CYP1A and CYP3A mRNAs by prototypical inducers in primary cultures of human, cynomolgus monkey, and rat hepatocytes
-
Nishimura, M., Koeda, A., Suganuma, Y., Suzuki, E., Shimizu, T., Nakayama, M., et al. (2007). Comparison of inducibility of CYP1A and CYP3A mRNAs by prototypical inducers in primary cultures of human, cynomolgus monkey, and rat hepatocytes. Drug Metab Pharmacokinet 22: 178-186.
-
(2007)
Drug Metab Pharmacokinet
, vol.22
, pp. 178-186
-
-
Nishimura, M.1
Koeda, A.2
Suganuma, Y.3
Suzuki, E.4
Shimizu, T.5
Nakayama, M.6
-
33
-
-
1542286164
-
Effect of rifampin on the pharmacokinetics of rosiglitazone in healthy subjects
-
Park, J. Y., Kim, K. A., Kang, M. H., Kim, S. L., Shin, J. G. (2004). Effect of rifampin on the pharmacokinetics of rosiglitazone in healthy subjects. Clin Pharmacol Ther 75: 157-162.
-
(2004)
Clin Pharmacol Ther
, vol.75
, pp. 157-162
-
-
Park, J.Y.1
Kim, K.A.2
Kang, M.H.3
Kim, S.L.4
Shin, J.G.5
-
34
-
-
33747868126
-
In vitro and in vivo CYP3A64 induction and inhibition studies in rhesus monkeys: A preclinical approach for CYP3A-mediated drug interaction studies
-
DOI 10.1124/dmd.106.009878
-
Prueksaritanont, T., Kuo, Y., Tang, C., Li, C., Qiu, Y., Lu, B., et al. (2006). In vitro and in vivo CYP3A64 induction and inhibition studies in rhesus monkeys: a preclinical approach for CYP3A-mediated drug interaction studies. Drug Metab Dispos 34: 1546-1555. (Pubitemid 44285397)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.9
, pp. 1546-1555
-
-
Prueksaritanont, T.1
Kuo, Y.2
Tang, C.3
Li, C.4
Qiu, Y.5
Lu, B.6
Strong-Basalyga, K.7
Richards, K.8
Carr, B.9
Lin, J.H.10
-
35
-
-
79851505734
-
Current in vitro high throughput screening approaches to assess nuclear receptor activation
-
Raucy, J. L., Lasker, J. M. (2010). Current in vitro high throughput screening approaches to assess nuclear receptor activation. Curr Drug Metab 11: 806-814.
-
(2010)
Curr Drug Metab
, vol.11
, pp. 806-814
-
-
Raucy, J.L.1
Lasker, J.M.2
-
36
-
-
61349172663
-
Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11beta-HSD1 inhibitors
-
Rew, Y., McMinn, D. L., Wang, Z., He, X., Hungate, R. W., Jaen, J. C., et al. (2009). Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11beta-HSD1 inhibitors. Bioorg Med Chem Lett 19: 1797-1801.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 1797-1801
-
-
Rew, Y.1
McMinn, D.L.2
Wang, Z.3
He, X.4
Hungate, R.W.5
Jaen, J.C.6
-
37
-
-
77955654799
-
Discovery and expanded SAR of 4,4-disubstituted quinazolin-2-ones as potent T-type calcium channel antagonists
-
Schlegel, K. A., Yang, Z. Q., Reger, T. S., Shu, Y., Cube, R., Rittle, K. E., et al. (2010). Discovery and expanded SAR of 4,4-disubstituted quinazolin-2-ones as potent T-type calcium channel antagonists. Bioorg Med Chem Lett 20: 5147-5152.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 5147-5152
-
-
Schlegel, K.A.1
Yang, Z.Q.2
Reger, T.S.3
Shu, Y.4
Cube, R.5
Rittle, K.E.6
-
38
-
-
0038434501
-
Artemisinin autoinduction is caused by involvement of cytochrome P450 2B6 but not 2C9
-
DOI 10.1016/S0009-9236(03)00092-4
-
Simonsson, U. S., Jansson, B., Hai, T. N., Huong, D. X., Tybring, G., Ashton, M. (2003). Artemisinin autoinduction is caused by involvement of cytochrome P450 2B6 but not 2C9. Clin Pharmacol Ther 74: 32-43. (Pubitemid 36776174)
-
(2003)
Clinical Pharmacology and Therapeutics
, vol.74
, Issue.1
, pp. 32-43
-
-
Simonsson, U.S.H.1
Jansson, B.2
Hai, T.N.3
Huong, D.X.4
Tybring, G.5
Ashton, M.6
-
39
-
-
33645972546
-
Stem cells, immortalized cells, and primary cells in ADMET assays
-
Sinz, M., Kim, S. (2006). Stem cells, immortalized cells, and primary cells in ADMET assays. Drug Discov Today Technol 3: 79-85.
-
(2006)
Drug Discov Today Technol
, vol.3
, pp. 79-85
-
-
Sinz, M.1
Kim, S.2
-
40
-
-
33646517938
-
Evaluation of 170 xenobiotics as transactivators of human pregnane X receptor (hPXR) and correlation to known CYP3A4 drug interactions
-
Sinz, M., Kim, S., Zhu, Z., Chen, T., Anthony, M., Dickinson, K., Rodrigues, A. D. (2006). Evaluation of 170 xenobiotics as transactivators of human pregnane X receptor (hPXR) and correlation to known CYP3A4 drug interactions. Curr Drug Metab 7: 375-388.
-
(2006)
Curr Drug Metab
, vol.7
, pp. 375-388
-
-
Sinz, M.1
Kim, S.2
Zhu, Z.3
Chen, T.4
Anthony, M.5
Dickinson, K.6
Rodrigues, A.D.7
-
41
-
-
53849093733
-
Current industrial practices in assessing CYP450 enzyme induction: Preclinical and clinical
-
Sinz, M., Wallace, G., Sahi, J. (2008). Current industrial practices in assessing CYP450 enzyme induction: preclinical and clinical. AAPS J 10: 391-400.
-
(2008)
AAPS J
, vol.10
, pp. 391-400
-
-
Sinz, M.1
Wallace, G.2
Sahi, J.3
-
42
-
-
78650175257
-
Regulation of drug-metabolizing enzymes by xenobiotic receptors: PXR and CAR
-
Tolson, A. H., Wang, H. (2010). Regulation of drug-metabolizing enzymes by xenobiotic receptors: PXR and CAR. Adv Drug Deliv Rev 62: 1238-1249.
-
(2010)
Adv Drug Deliv Rev
, vol.62
, pp. 1238-1249
-
-
Tolson, A.H.1
Wang, H.2
-
43
-
-
0037501542
-
2.1 crystal structure of human PXR in complex with the St. John's wort compound hyperforin
-
DOI 10.1021/bi0268753
-
Watkins, R. E., Maglich, J. M., Moore, L. B., Wisely, G. B., Noble, S. M., Davis-Searles, P. R., et al. (2003). 2.1 A crystal structure of human PXR in complex with the St. John's wort compound hyperforin. Biochemistry 42: 1430-1438. (Pubitemid 36205949)
-
(2003)
Biochemistry
, vol.42
, Issue.6
, pp. 1430-1438
-
-
Watkins, R.E.1
Maglich, J.M.2
Moore, L.B.3
Wisely, G.B.4
Noble, S.M.5
Davis-Searles, P.R.6
Lambert, M.H.7
Kliewer, S.A.8
Redinbo, M.R.9
-
44
-
-
0035933511
-
The human nuclear xenobiotic receptor PXR: Structural determinants of directed promiscuity
-
DOI 10.1126/science.1060762
-
Watkins, R. E., Wisely, G. B., Moore, L. B., Collins, J. L., Lambert, M. H., Williams, S. P., et al. (2001). The human nuclear xenobiotic receptor PXR: structural determinants of directed promiscuity. Science 292: 2329-2333. (Pubitemid 32568055)
-
(2001)
Science
, vol.292
, Issue.5525
, pp. 2329-2333
-
-
Watkins, R.E.1
Wisely, G.B.2
Moore, L.B.3
Collins, J.L.4
Lambert, M.H.5
Williams, S.P.6
Willson, T.M.7
Kliewer, S.A.8
Redinbo, M.R.9
-
45
-
-
34447133457
-
New opportunities for pregnane X receptor (PXR) targeting in drug development. Lessons from enantio- and species-specific PXR ligands identified from a discovery library of amino acid analogues
-
DOI 10.2174/138955707780859404
-
Wipf, P., Gong, H., Janjic, J. M., Li, S., Day, B. W., Xie, W. (2007). New opportunities for pregnane X receptor (PXR) targeting in drug development. Lessons from Enantio-and species-specific PXR ligands identified from a discovery library of amino acid analogues. Mini Rev Med Chem 7: 617-625. (Pubitemid 47099182)
-
(2007)
Mini-Reviews in Medicinal Chemistry
, vol.7
, Issue.6
, pp. 617-625
-
-
Wipf, P.1
Gong, H.2
Janjic, J.M.3
Li, S.4
Day, B.W.5
Xie, W.6
-
46
-
-
0034831129
-
Implications and consequences of enzyme induction on preclinical and clinical drug development
-
DOI 10.1080/00498250110054623
-
Worboys, P. D., Carlile, D. J. (2001). Implications and consequences of enzyme induction on preclinical and clinical drug development. Xenobiotica 31: 539-556. (Pubitemid 32826391)
-
(2001)
Xenobiotica
, vol.31
, Issue.8-9
, pp. 539-556
-
-
Worboys, P.D.1
Carlile, D.J.2
-
47
-
-
34250832009
-
Crystal structure of the pregnane X receptor-estradiol complex provides insights into endobiotic recognition
-
DOI 10.1210/me.2006-0323
-
Xue, Y., Moore, L. B., Orans, J., Peng, L., Bencharit, S., Kliewer, S. A., et al. (2007). Crystal structure of the pregnane X receptor-estradiol complex provides insights into endobiotic recognition. Mol Endocrinol 21: 1028-1038. (Pubitemid 46984756)
-
(2007)
Molecular Endocrinology
, vol.21
, Issue.5
, pp. 1028-1038
-
-
Xue, Y.1
Moore, L.B.2
Orans, J.3
Peng, L.4
Bencharit, S.5
Kliewer, S.A.6
Redinbo, M.R.7
-
48
-
-
65349091444
-
The steroid and xenobiotic receptor (SXR), beyond xenobiotic metabolism
-
Zhou, C., Verma, S., Blumberg, B. (2009). The steroid and xenobiotic receptor (SXR), beyond xenobiotic metabolism. Nucl Recept Signal 7: e001.
-
(2009)
Nucl Recept Signal
, vol.7
-
-
Zhou, C.1
Verma, S.2
Blumberg, B.3
-
49
-
-
16644388319
-
Correlation of high-throughput pregnane X receptor (PXR) transactivation and binding assays
-
Zhu, Z., Kim, S., Chen, T., Lin, J. H., Bell, A., Bryson, J., et al. (2004). Correlation of high-throughput pregnane X receptor (PXR) transactivation and binding assays. J Biomol Screen 9: 533-540.
-
(2004)
J Biomol Screen
, vol.9
, pp. 533-540
-
-
Zhu, Z.1
Kim, S.2
Chen, T.3
Lin, J.H.4
Bell, A.5
Bryson, J.6
-
50
-
-
33847614798
-
Use of cryopreserved transiently transfected cells in high-throughput pregnane X receptor transactivation assay
-
DOI 10.1177/1087057106297828
-
Zhu, Z., Puglisi, J., Connors, D., Stewart, J., Herbst, J., Marino, A., et al. (2007). Use of cryopreserved transiently transfected cells in highthroughput pregnane X receptor transactivation assay. J Biomol Screen 12: 248-254. (Pubitemid 46364431)
-
(2007)
Journal of Biomolecular Screening
, vol.12
, Issue.2
, pp. 248-254
-
-
Zhu, Z.1
Puglisi, J.2
Connors, D.3
Stewart, J.4
Herbst, J.5
Marino, A.6
Sinz, M.7
O'Connell, J.8
Banks, M.9
Dickinson, K.10
Cacace, A.11
-
51
-
-
76649090591
-
SAR of PXR transactivation in benzimidazole-based IGF-1R kinase inhibitors
-
Zimmermann, K., Wittman, M. D., Saulnier, M. G., Velaparthi, U., Sang, X., Frennesson, D. B., et al. (2010). SAR of PXR transactivation in benzimidazole-based IGF-1R kinase inhibitors. Bioorg Med Chem Lett 20: 1744-1748.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1744-1748
-
-
Zimmermann, K.1
Wittman, M.D.2
Saulnier, M.G.3
Velaparthi, U.4
Sang, X.5
Frennesson, D.B.6
|