-
1
-
-
33748042671
-
Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3- methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: Drug-drug interactions and interindividual differences in transporter and metabolic enzyme functions
-
DOI 10.1016/j.pharmthera.2006.03.003, PII S0163725806000404
-
Shitara Y, Sugiyama Y. Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: drug-drug interactions and interindividual differences in transporter and metabolic enzyme functions. Pharmacol Ther. 2006 ; 112: 71-105 (Pubitemid 44301483)
-
(2006)
Pharmacology and Therapeutics
, vol.112
, Issue.1
, pp. 71-105
-
-
Shitara, Y.1
Sugiyama, Y.2
-
2
-
-
47949090855
-
-
You G Morris ME, ed. Hoboken, NJ: John Wiley;
-
Tirona RG, Kim RB Drug Transporters. You G Morris ME, ed. Hoboken, NJ: John Wiley ; 75-104.
-
Drug Transporters
, pp. 75-104
-
-
Tirona, R.G.1
Kim, R.B.2
-
3
-
-
0030812885
-
In vitro metabolism of simvastatin in humans [SBT]identification of metabolizlng enzymes and effect of the drug on hepatic P450S
-
Prueksaritanont T, Gorham LM, Ma B, et al. In vitro metabolism of simvastatin in humans [SBT]identification of metabolizing enzymes and effect of the drug on hepatic P450s. Drug Metab Dispos. 1997 ; 25: 1191-1199 (Pubitemid 27446590)
-
(1997)
Drug Metabolism and Disposition
, vol.25
, Issue.10
, pp. 1191-1199
-
-
Prueksaritanont, T.1
Gorham, L.M.2
Ma, B.3
Liu, L.4
Yu, X.5
Zhao, J.J.6
Slaughter, D.E.7
Arison, B.H.8
Vyas, K.P.9
-
4
-
-
0033783036
-
Lactonization is the critical first step in the disposition of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor atorvastatin
-
Jacobsen W, Kuhn B, Soldner A, et al. Lactonization is the critical first step in the disposition of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor atorvastatin. Drug Metab Dispos. 2000 ; 28: 1369-1378
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 1369-1378
-
-
Jacobsen, W.1
Kuhn, B.2
Soldner, A.3
-
5
-
-
0035825928
-
Preclinical and clinical pharmacology of rosuvastatin, a new 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor
-
PII S0002914901014540
-
McTaggart F, Buckett L, Davidson R, et al. Preclinical and clinical pharmacology of Rosuvastatin, a new 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor. Am J Cardiol. 2001 ; 87 (5A). 28B - 32B (Pubitemid 32274242)
-
(2001)
American Journal of Cardiology
, vol.87
, Issue.5 SUPPL. 1
-
-
McTaggart, F.1
Buckett, L.2
Davidson, R.3
Holdgate, G.4
McCormick, A.5
Schneck, D.6
Smith, G.7
Warwick, M.8
-
6
-
-
0000626919
-
ZD4522-an HMG-CoA reductase inhibitor free of metabolically mediated drug interactions: Metabolic studies in human in vitro systems [abstract]
-
McCormick AD, McKillop D, Butters CJ, et al. ZD4522-an HMG-CoA reductase inhibitor free of metabolically mediated drug interactions: metabolic studies in human in vitro systems [abstract]. J Clin Pharmacol. 2000 1055 ; 40 :
-
(2000)
J Clin Pharmacol
, vol.1055
, pp. 40
-
-
McCormick, A.D.1
McKillop, D.2
Butters, C.J.3
-
7
-
-
47949104688
-
Targeted disruption of murine organic anion-transporting polypeptide 1b2 (Oatp1b2/Slco1b2) significantly alters disposition of prototypical drug substrates pravastatin and rifampin
-
Zaher H, zu Schwabedissen HE, Tirona RG, et al. Targeted disruption of murine organic anion-transporting polypeptide 1b2 (Oatp1b2/Slco1b2) significantly alters disposition of prototypical drug substrates pravastatin and rifampin. Mol Pharmacol. 2008 ; 74: 320-329
-
(2008)
Mol Pharmacol
, vol.74
, pp. 320-329
-
-
Zaher, H.1
Zu Schwabedissen, H.E.2
Tirona, R.G.3
-
8
-
-
50049110841
-
Utility of a novel Oatp1b2 knockout mouse model for evaluating the role of Oatp1b2 in the hepatic uptake of model compounds
-
Chen C, Stock JL, Liu X, et al. Utility of a novel Oatp1b2 knockout mouse model for evaluating the role of Oatp1b2 in the hepatic uptake of model compounds. Drug Metab Dispos. 2008 ; 36: 1840-1845
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 1840-1845
-
-
Chen, C.1
Stock, J.L.2
Liu, X.3
-
9
-
-
72849141790
-
Transporter pharmacogenetics and statin toxicity
-
Niemi M. Transporter pharmacogenetics and statin toxicity. Clin Pharmacol Ther. 2010 ; 87: 130-133
-
(2010)
Clin Pharmacol Ther
, vol.87
, pp. 130-133
-
-
Niemi, M.1
-
10
-
-
15744367808
-
Polymorphisms in human organic anion-transporting polypeptide 1A2 (OATP1A2): Implications for altered drug disposition and central nervous system drug entry
-
DOI 10.1074/jbc.M411092200
-
Lee W, Glaeser H, Smith LH, et al. Polymorphisms in human organic anion-transporting polypeptide 1A2 (OATP1A2): implications for altered drug disposition and central nervous system drug entry. J Biol Chem. 2005 ; 280: 9610-9617 (Pubitemid 40409657)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.10
, pp. 9610-9617
-
-
Lee, W.1
Glaeser, H.2
Smith, L.H.3
Roberts, R.L.4
Moeckel, G.W.5
Gervasini, G.6
Leake, B.F.7
Kim, R.B.8
-
11
-
-
77955300958
-
Organic anion transporting polypeptide 1a/1b-knockout mice provide insights into hepatic handling of bilirubin, bile acids, and drugs
-
van de, Steeg E, Wagenaar E, van der Kruijssen CM, et al. Organic anion transporting polypeptide 1a/1b-knockout mice provide insights into hepatic handling of bilirubin, bile acids, and drugs. J Clin Invest. 2010 ; 120: 2942-2952
-
(2010)
J Clin Invest
, vol.120
, pp. 2942-2952
-
-
De Van1
Steeg, E.2
Wagenaar, E.3
Van Der Kruijssen, C.M.4
-
12
-
-
79251491062
-
High impact of Oatp1a/1b transporters on in vivo disposition of the hydrophobic anticancer drug paclitaxel
-
Van de, Steeg E, van Esch A, Wagenaar E, et al. High impact of Oatp1a/1b transporters on in vivo disposition of the hydrophobic anticancer drug paclitaxel. Clin Cancer Res. 2010 ; 17: 294-301
-
(2010)
Clin Cancer Res
, vol.17
, pp. 294-301
-
-
Van De1
Steeg, E.2
Van Esch, A.3
Wagenaar, E.4
-
13
-
-
36148953896
-
Different effects of SLCO1B1 polymorphism on the pharmacokinetics of atorvastatin and rosuvastatin
-
DOI 10.1038/sj.clpt.6100220, PII 6100220
-
Pasanen MK, Fredrikson H, Neuvonen PJ, Niemi M. Different effects of SLCO1B1 polymorphism on the pharmacokinetics of atorvastatin and rosuvastatin. Clin Pharmacol Ther. 2007 ; 82: 726-733 (Pubitemid 350114817)
-
(2007)
Clinical Pharmacology and Therapeutics
, vol.82
, Issue.6
, pp. 726-733
-
-
Pasanen, M.K.1
Fredrikson, H.2
Neuvonen, P.J.3
Niemi, M.4
-
14
-
-
0038336614
-
The human hepatic metabolism of simvastatin hydroxy acid is mediated primarily by CYP3A, and not CYP2D6
-
DOI 10.1046/j.1365-2125.2003.01833.x
-
Prueksaritanont T, Ma B, Yu N. The human hepatic metabolism of simvastatin hydroxy acid is mediated primarily by CYP3A, and not CYP2D6. Br J Clin Pharmacol. 2003 ; 56: 120-124 (Pubitemid 36886497)
-
(2003)
British Journal of Clinical Pharmacology
, vol.56
, Issue.1
, pp. 120-124
-
-
Prueksaritanont, T.1
Ma, B.2
Yu, N.3
-
15
-
-
0344664550
-
Metabolism, Excretion, and Pharmacokinetics of Rosuvastatin in Healthy Adult Male Volunteers
-
DOI 10.1016/S0149-2918(03)80336-3
-
Martin PD, Warwick MJ, Dane AL, et al. Metabolism, excretion, and pharmacokinetics of rosuvastatin in healthy adult male volunteers. Clin Ther. 2003 ; 25: 2822-2835 (Pubitemid 37510592)
-
(2003)
Clinical Therapeutics
, vol.25
, Issue.11
, pp. 2822-2835
-
-
Martin, P.D.1
Warwick, M.J.2
Dane, A.L.3
Hill, S.J.4
Giles, P.B.5
Phillips, P.J.6
Lenz, E.7
-
16
-
-
33646536542
-
Drug and bile acid transporters in rosuvastatin hepatic uptake: Function, expression, and pharmacogenetics
-
Ho RH, Tirona RG, Leake BF, et al. Drug and bile acid transporters in rosuvastatin hepatic uptake: function, expression, and pharmacogenetics. Gastroenterology. 2006 ; 130: 1793-1806
-
(2006)
Gastroenterology
, vol.130
, pp. 1793-1806
-
-
Ho, R.H.1
Tirona, R.G.2
Leake, B.F.3
-
17
-
-
52949104006
-
Involvement of multiple transporters in the hepatobiliary transport of rosuvastatin
-
Kitamura S, Maeda K, Wang Y, Sugiyama Y. Involvement of multiple transporters in the hepatobiliary transport of rosuvastatin. Drug Metab Dispos. 2008 ; 36: 2014-2023
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 2014-2023
-
-
Kitamura, S.1
Maeda, K.2
Wang, Y.3
Sugiyama, Y.4
-
18
-
-
22544454498
-
Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15 + C1007G, by using transient expression systems of HeLa and HEK293 cells
-
Kameyama Y, Yamashita K, Kobayashi K, Hosokawa M, Chiba K. Functional characterization of SLCO1B1 (OATP-C) variants, SLCO1B1*5, SLCO1B1*15 and SLCO1B1*15+C1007G, by using transient expression systems of HeLa and HEK293 cells. Pharmacogenet Genomics. 2005 ; 15: 513-522 (Pubitemid 41017600)
-
(2005)
Pharmacogenetics and Genomics
, vol.15
, Issue.7
, pp. 513-522
-
-
Kameyama, Y.1
Yamashita, K.2
Kobayashi, K.3
Hosokawa, M.4
Chiba, K.5
-
19
-
-
0033601257
-
A novel human hepatic organic anion transporting polypeptide (OATP2): Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl- CoA reductase inhibitor transporters
-
Hsiang B, Zhu Y, Wang Z, et al. A novel human hepatic organic anion transporting polypeptide (OATP2): identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl- CoA reductase inhibitor transporters. J Biol Chem. 1999 ; 274: 37161-37168
-
(1999)
J Biol Chem
, vol.274
, pp. 37161-37168
-
-
Hsiang, B.1
Zhu, Y.2
Wang, Z.3
-
20
-
-
15344341734
-
Differential interaction of 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors with ABCB1, ABCC2, and OATP1B1
-
DOI 10.1124/dmd.104.002477
-
Chen C, Mireles RJ, Campbell SD, et al. Differential interaction of 3-hydroxy-3-methylglutaryl-coa reductase inhibitors with ABCB1, ABCC2, and OATP1B1. Drug Metab Dispos. 2005 ; 33: 537-546 (Pubitemid 40393197)
-
(2005)
Drug Metabolism and Disposition
, vol.33
, Issue.4
, pp. 537-546
-
-
Chen, C.1
Mireles, R.J.2
Campbell, S.D.3
Lin, J.4
Mills, J.B.5
Xu, J.J.6
Smolarek, T.A.7
-
21
-
-
33751096467
-
SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid
-
DOI 10.1097/01.fpc.0000230416.82349.90, PII 0121301120061200000004
-
Pasanen MK, Neuvonen M, Neuvonen PJ, Niemi M. SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid. Pharmacogenet Genomics. 2006 ; 16: 873-879 (Pubitemid 44772805)
-
(2006)
Pharmacogenetics and Genomics
, vol.16
, Issue.12
, pp. 873-879
-
-
Pasanen, M.K.1
Neuvonen, M.2
Neuvonen, P.J.3
Niemi, M.4
-
22
-
-
16244396867
-
Interactions of human P-glycoprotein with simvastatin, simvastatin acid, and atorvastatin
-
DOI 10.1023/B:PHAM.0000041466.84653.8c
-
Hochman JH, Pudvah N, Qiu J, et al. Interactions of human P-glycoprotein with simvastatin, simvastatin acid, and atorvastatin. Pharm Res. 2004 ; 21: 1686-1691 (Pubitemid 41184401)
-
(2004)
Pharmaceutical Research
, vol.21
, Issue.9
, pp. 1686-1691
-
-
Hochman, J.H.1
Pudvah, N.2
Qiu, J.3
Yamazaki, M.4
Tang, C.5
Lin, J.H.6
Prueksaritanont, T.7
-
23
-
-
67249111853
-
Narrative review: Statin-related myopathy
-
Joy TR, Hegele RA. Narrative review: statin-related myopathy. Ann Intern Med. 2009 ; 150: 858-868
-
(2009)
Ann Intern Med
, vol.150
, pp. 858-868
-
-
Joy, T.R.1
Hegele, R.A.2
-
24
-
-
78951469667
-
Common nonsynonymous substitutions in SLCO1B1 predispose to statin intolerance in routinely treated individuals with type 2 diabetes: A go-DARTS study
-
Donnelly LA, Doney AS, Tavendale R, et al. Common nonsynonymous substitutions in SLCO1B1 predispose to statin intolerance in routinely treated individuals with type 2 diabetes: a go-DARTS study. Clin Pharmacol Ther. 2011 ; 89: 210-216
-
(2011)
Clin Pharmacol Ther
, vol.89
, pp. 210-216
-
-
Donnelly, L.A.1
Doney, A.S.2
Tavendale, R.3
-
25
-
-
0035218021
-
In-vivo phenotyping for CYP3A by a single-point determination of midazolam plasma concentration
-
DOI 10.1097/00008571-200112000-00006
-
Lin YS, Lockwood GF, Graham MA, et al. In-vivo phenotyping for CYP3A by a single-point determination of midazolam plasma concentration. Pharmacogenetics. 2001 ; 11: 781-791 (Pubitemid 33151513)
-
(2001)
Pharmacogenetics
, vol.11
, Issue.9
, pp. 781-791
-
-
Lin, Y.S.1
Lockwood, G.F.2
Graham, M.A.3
Brian, W.R.4
Loi, C.-M.5
Dobrinska, M.R.6
Shen, D.D.7
Watkins, P.B.8
Wilkinson, G.R.9
Kharasch, E.D.10
Thummel, K.E.11
|