-
1
-
-
84877850880
-
Review of P-gp inhibition data in recently approved new drug applications: Utility of the proposed [I(1) ]/IC(50) and [I(2) ]/IC(50) criteria in the P-gp decision tree
-
Agarwal S, Arya V, and Zhang L (2013) Review of P-gp inhibition data in recently approved new drug applications: utility of the proposed [I(1) ]/IC(50) and [I(2) ]/IC(50) criteria in the P-gp decision tree. J Clin Pharmacol 53:228-233.
-
(2013)
J Clin Pharmacol
, vol.53
, pp. 228-233
-
-
Agarwal, S.1
Arya, V.2
Zhang, L.3
-
2
-
-
84879085257
-
50) using various in vitro experimental systems: Implications for universal digoxin DDI risk assessment decision criteria
-
50) using various in vitro experimental systems: implications for universal digoxin DDI risk assessment decision criteria. Drug Metab Dispos 41:1347-1366.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 1347-1366
-
-
Bentz, J.E.1
O'Connor, M.2
Bednarczyk, D.3
Coleman, J.4
Lee, C.A.5
Palm, J.E.6
Pak, A.7
Perloff, E.S.8
Reyner, E.L.9
Balimane, P.10
-
3
-
-
77955851957
-
In vitro interactions between aged garlic extract and drugs used for the treatment of cardiovascular and diabetic patients
-
Berginc K, Žakelj S, and Kristl A (2010) In vitro interactions between aged garlic extract and drugs used for the treatment of cardiovascular and diabetic patients. Eur J Nutr 49:373-384.
-
(2010)
Eur J Nutr
, vol.49
, pp. 373-384
-
-
Berginc, K.1
Žakelj, S.2
Kristl, A.3
-
4
-
-
84877635707
-
PK/PD assessment in CNS drug discovery: Prediction of CSF concentration in rodents for P-glycoprotein substrates and application to in vivo potency estimation
-
Caruso A, Alvarez-Sánchez R, Hillebrecht A, Poirier A, Schuler F, Lavé T, Funk C, and Belli S (2013) PK/PD assessment in CNS drug discovery: Prediction of CSF concentration in rodents for P-glycoprotein substrates and application to in vivo potency estimation. Biochem Pharmacol 85:1684-1699.
-
(2013)
Biochem Pharmacol
, vol.85
, pp. 1684-1699
-
-
Caruso, A.1
Alvarez-Sánchez, R.2
Hillebrecht, A.3
Poirier, A.4
Schuler, F.5
Lavé, T.6
Funk, C.7
Belli, S.8
-
5
-
-
0037372571
-
P-glycoprotein limits the brain penetration of nonsedating but not sedating H1-antagonists
-
DOI 10.1124/dmd.31.3.312
-
Chen C, Hanson E, Watson JW, and Lee JS (2003) P-glycoprotein limits the brain penetration of nonsedating but not sedating H1-antagonists. Drug Metab Dispos 31:312-318. (Pubitemid 36249686)
-
(2003)
Drug Metabolism and Disposition
, vol.31
, Issue.3
, pp. 312-318
-
-
Chen, C.1
Hanson, E.2
Watson, J.W.3
Lee, J.S.4
-
6
-
-
77950571874
-
Refining the in vitro and in vivo critical parameters for P-glycoprotein, [I]/IC50 and [I2]/IC50, that allow for the exclusion of drug candidates from clinical digoxin interaction studies
-
Cook JA, Feng B, Fenner KS, Kempshall S, Liu R, Rotter C, Smith DA, Troutman MD, Ullah M, and Lee CA (2010) Refining the in vitro and in vivo critical parameters for P-glycoprotein, [I]/IC50 and [I2]/IC50, that allow for the exclusion of drug candidates from clinical digoxin interaction studies. Mol Pharm 7:398-411.
-
(2010)
Mol Pharm
, vol.7
, pp. 398-411
-
-
Cook, J.A.1
Feng, B.2
Fenner, K.S.3
Kempshall, S.4
Liu, R.5
Rotter, C.6
Smith, D.A.7
Troutman, M.D.8
Ullah, M.9
Lee, C.A.10
-
7
-
-
0033323809
-
FDA evaluations using in vitro metabolism to predict and interpret in vivo metabolic drug-drug interactions: Impact on labeling
-
Davit B, Reynolds K, Yuan R, Ajayi F, Conner D, Fadiran E, Gillespie B, Sahajwalla C, Huang SM, and Lesko LJ (1999) FDA evaluations using in vitro metabolism to predict and interpret in vivo metabolic drug-drug interactions: impact on labeling. J Clin Pharmacol 39:899-910. (Pubitemid 30644025)
-
(1999)
Journal of Clinical Pharmacology
, vol.39
, Issue.9
, pp. 899-910
-
-
Davit, B.1
Reynolds, K.2
Yuan, R.3
Ajayi, F.4
Conner, D.5
Fadiran, E.6
Gillespie, B.7
Sahajwalla, C.8
Huang, S.-M.9
Lesko, L.J.10
-
8
-
-
84879096812
-
Application of receiver operating characteristic analysis to refine the prediction of potential digoxin drug interactions
-
Ellens H, Deng S, Coleman J, Bentz J, Taub ME, Ragueneau-Majlessi I, Chung SP, Herédi-Szabó K, Neuhoff S, and Palm J, et al. (2013) Application of receiver operating characteristic analysis to refine the prediction of potential digoxin drug interactions. Drug Metab Dispos 41:1367-1374.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 1367-1374
-
-
Ellens, H.1
Deng, S.2
Coleman, J.3
Bentz, J.4
Taub, M.E.5
Ragueneau-Majlessi, I.6
Chung, S.P.7
Herédi-Szabó, K.8
Neuhoff, S.9
Palm, J.10
-
9
-
-
79251518645
-
The utility of in vitro data in making accurate predictions of human P-glycoprotein-mediated drug-drug interactions: A case study for AZD5672
-
Elsby R, Gillen M, Butters C, Imisson G, Sharma P, Smith V, and Surry DD (2011) The utility of in vitro data in making accurate predictions of human P-glycoprotein-mediated drug-drug interactions: a case study for AZD5672. Drug Metab Dispos 39:275-282.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 275-282
-
-
Elsby, R.1
Gillen, M.2
Butters, C.3
Imisson, G.4
Sharma, P.5
Smith, V.6
Surry, D.D.7
-
10
-
-
0345438685
-
ROC graphs: Notes and practical considerations for data mining researchers
-
Hewlett-Packard Labs, Palo Alto, CA
-
Fawcett T (2004) ROC graphs: notes and practical considerations for data mining researchers. Technical Report HPL-2003-4. Hewlett-Packard Labs, Palo Alto, CA.
-
(2004)
Technical Report HPL-2003-4
-
-
Fawcett, T.1
-
11
-
-
58549088199
-
Drug-drug interactions mediated through P-glycoprotein: Clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug
-
Fenner KS, Troutman MD, Kempshall S, Cook JA, Ware JA, Smith DA, and Lee CA (2009) Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug. Clin Pharmacol Ther 85:173-181.
-
(2009)
Clin Pharmacol Ther
, vol.85
, pp. 173-181
-
-
Fenner, K.S.1
Troutman, M.D.2
Kempshall, S.3
Cook, J.A.4
Ware, J.A.5
Smith, D.A.6
Lee, C.A.7
-
12
-
-
77953737073
-
Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data
-
Gertz M, Harrison A, Houston JB, and Galetin A (2010) Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data. Drug Metab Dispos 38:1147-1158.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 1147-1158
-
-
Gertz, M.1
Harrison, A.2
Houston, J.B.3
Galetin, A.4
-
13
-
-
77649216536
-
Membrane transporters in drug development
-
International Transporter Consortium
-
Giacomini KM, Huang SM, Tweedie DJ, Benet LZ, Brouwer KL, Chu X, Dahlin A, Evers R, Fischer V, and Hillgren KM, et al.; International Transporter Consortium (2010) Membrane transporters in drug development. Nat Rev Drug Discov 9:215-236.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 215-236
-
-
Giacomini, K.M.1
Huang, S.M.2
Tweedie, D.J.3
Benet, L.Z.4
Brouwer, K.L.5
Chu, X.6
Dahlin, A.7
Evers, R.8
Fischer, V.9
Hillgren, K.M.10
-
14
-
-
79959522836
-
In vitro and in vivo P-glycoprotein transport characteristics of rivaroxaban
-
Gnoth MJ, Buetehorn U, Muenster U, Schwarz T, and Sandmann S (2011) In vitro and in vivo P-glycoprotein transport characteristics of rivaroxaban. J Pharmacol Exp Ther 338:372-380.
-
(2011)
J Pharmacol Exp Ther
, vol.338
, pp. 372-380
-
-
Gnoth, M.J.1
Buetehorn, U.2
Muenster, U.3
Schwarz, T.4
Sandmann, S.5
-
15
-
-
0032823160
-
Intestinal secretion of intravenous talinolol is inhibited by luminal R- verapamil
-
DOI 10.1016/S0009-9236(99)70031-7
-
Gramatté T and Oertel R (1999) Intestinal secretion of intravenous talinolol is inhibited by luminal R-verapamil. Clin Pharmacol Ther 66:239-245. (Pubitemid 29451755)
-
(1999)
Clinical Pharmacology and Therapeutics
, vol.66
, Issue.3
, pp. 239-245
-
-
Gramatte, T.1
Oertel, R.2
-
16
-
-
0029999340
-
Direct demonstration of small intestinal secretion and site-dependent absorption of the beta-blocker talinolol in humans
-
DOI 10.1016/S0009-9236(96)90182-4
-
Gramatté T, Oertel R, Terhaag B, and Kirch W (1996) Direct demonstration of small intestinal secretion and site-dependent absorption of the beta-blocker talinolol in humans. Clin Pharmacol Ther 59:541-549. (Pubitemid 26191376)
-
(1996)
Clinical Pharmacology and Therapeutics
, vol.59
, Issue.5
, pp. 541-549
-
-
Gramatte, T.1
Oertel, R.2
Terhaag, B.3
Kirch, W.4
-
17
-
-
34748829961
-
Oxycodone induces overexpression of P-glycoprotein (ABCB1) and affects paclitaxel's tissue distribution in sprague dawley rats
-
DOI 10.1002/jps.20893
-
Hassan HE, Myers AL, Lee IJ, Coop A, and Eddington ND (2007) Oxycodone induces overexpression of P-glycoprotein (ABCB1) and affects paclitaxel's tissue distribution in Sprague Dawley rats. J Pharm Sci 96:2494-2506. (Pubitemid 47477902)
-
(2007)
Journal of Pharmaceutical Sciences
, vol.96
, Issue.9
, pp. 2494-2506
-
-
Hassan, H.E.1
Myers, A.L.2
Lee, I.J.3
Coop, A.4
Eddington, N.D.5
-
18
-
-
84867848663
-
Comparison of brain capillary endothelial cell-based and epithelial (MDCK-MDR1, Caco-2, and VB-Caco-2) cell-based surrogate blood-brain barrier penetration models
-
Hellinger E, Veszelka S, Tóth AE, Walter F, Kittel A, Bakk ML, Tihanyi K, Háda V, Nakagawa S, and Duy TD, et al. (2012) Comparison of brain capillary endothelial cell-based and epithelial (MDCK-MDR1, Caco-2, and VB-Caco-2) cell-based surrogate blood-brain barrier penetration models. Eur J Pharm Biopharm 82:340-351.
-
(2012)
Eur J Pharm Biopharm
, vol.82
, pp. 340-351
-
-
Hellinger, E.1
Veszelka, S.2
Tóth, A.E.3
Walter, F.4
Kittel, A.5
Bakk, M.L.6
Tihanyi, K.7
Háda, V.8
Nakagawa, S.9
Duy, T.D.10
-
19
-
-
84891762128
-
Impact of endogenous esterase activity on in vitro p-glycoprotein profiling of dabigatran etexilate in Caco-2 monolayers
-
Ishiguro N, Kishimoto W, Volz A, Ludwig-Schwellinger E, Ebner T, and Schaefer O (2014) Impact of endogenous esterase activity on in vitro p-glycoprotein profiling of dabigatran etexilate in Caco-2 monolayers. Drug Metab Dispos 42:250-256.
-
(2014)
Drug Metab Dispos
, vol.42
, pp. 250-256
-
-
Ishiguro, N.1
Kishimoto, W.2
Volz, A.3
Ludwig-Schwellinger, E.4
Ebner, T.5
Schaefer, O.6
-
21
-
-
84879415192
-
Why clinical modulation of efflux transport at the human blood-brain barrier is unlikely: The ITC evidence-based position
-
International Transporter Consortium
-
Kalvass JC, Polli JW, Bourdet DL, Feng B, Huang SM, Liu X, Smith QR, Zhang LK, and Zamek-Gliszczynski MJ; International Transporter Consortium (2013) Why clinical modulation of efflux transport at the human blood-brain barrier is unlikely: the ITC evidence-based position. Clin Pharmacol Ther 94:80-94.
-
(2013)
Clin Pharmacol Ther
, vol.94
, pp. 80-94
-
-
Kalvass, J.C.1
Polli, J.W.2
Bourdet, D.L.3
Feng, B.4
Huang, S.M.5
Liu, X.6
Smith, Q.R.7
Zhang, L.K.8
Zamek-Gliszczynski, M.J.9
-
22
-
-
68949202522
-
Uptake/efflux transport of tramadol enantiomers and O-desmethyl-tramadol: Focus on P-glycoprotein
-
Kanaan M, Daali Y, Dayer P, and Desmeules J (2009) Uptake/efflux transport of tramadol enantiomers and O-desmethyl-tramadol: focus on P-glycoprotein. Basic Clin Pharmacol Toxicol 105:199-206.
-
(2009)
Basic Clin Pharmacol Toxicol
, vol.105
, pp. 199-206
-
-
Kanaan, M.1
Daali, Y.2
Dayer, P.3
Desmeules, J.4
-
23
-
-
0036775041
-
Review of fexofenadine in the treatment of chronic idiopathic urticaria
-
DOI 10.1046/j.1365-4362.2002.01599.x
-
Kawashima M, Harada S, and Tango T (2002) Review of fexofenadine in the treatment of chronic idiopathic urticaria. Int J Dermatol 41:701-706. (Pubitemid 35252053)
-
(2002)
International Journal of Dermatology
, vol.41
, Issue.10
, pp. 701-706
-
-
Kawashima, M.1
Harada, S.2
Tango, T.3
-
24
-
-
77952239982
-
Pharmacokinetics of fexofenadine: Evaluation of a microdose and assessment of absolute oral bioavailability
-
Lappin G, Shishikura Y, Jochemsen R, Weaver RJ, Gesson C, Houston B, Oosterhuis B, Bjerrum OJ, Rowland M, and Garner C (2010) Pharmacokinetics of fexofenadine: evaluation of a microdose and assessment of absolute oral bioavailability. Eur J Pharm Sci 40:125-131.
-
(2010)
Eur J Pharm Sci
, vol.40
, pp. 125-131
-
-
Lappin, G.1
Shishikura, Y.2
Jochemsen, R.3
Weaver, R.J.4
Gesson, C.5
Houston, B.6
Oosterhuis, B.7
Bjerrum, O.J.8
Rowland, M.9
Garner, C.10
-
25
-
-
0036896304
-
Passive permeability and P-glycoprotein-mediated efflux differentiate central nervous system (CNS) and non-CNS marketed drugs
-
DOI 10.1124/jpet.102.039255
-
Mahar Doan KM, Humphreys JE, Webster LO, Wring SA, Shampine LJ, Serabjit-Singh CJ, Adkison KK, and Polli JW (2002) Passive permeability and P-glycoprotein-mediated efflux differentiate central nervous system (CNS) and non-CNS marketed drugs. J Pharmacol Exp Ther 303:1029-1037. (Pubitemid 35424386)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.303
, Issue.3
, pp. 1029-1037
-
-
Mahar, D.K.M.1
Humphreys, J.E.2
Webster, L.O.3
Wring, S.A.4
Shampine, L.J.5
Serabjit-Singh, C.J.6
Adkison, K.K.7
Polli, J.W.8
-
26
-
-
84859435363
-
Determining P-glycoprotein-drug interactions: Evaluation of reconstituted P-glycoprotein in a liposomal system and LLC-MDR1 polarized cell monolayers
-
Melchior DL, Sharom FJ, Evers R, Wright GE, Chu JW, Wright SE, Chu X, and Yabut J (2012) Determining P-glycoprotein-drug interactions: evaluation of reconstituted P-glycoprotein in a liposomal system and LLC-MDR1 polarized cell monolayers. J Pharmacol Toxicol Methods 65:64-74.
-
(2012)
J Pharmacol Toxicol Methods
, vol.65
, pp. 64-74
-
-
Melchior, D.L.1
Sharom, F.J.2
Evers, R.3
Wright, G.E.4
Chu, J.W.5
Wright, S.E.6
Chu, X.7
Yabut, J.8
-
27
-
-
80051773262
-
Relationship between P-glycoprotein and second-generation antipsychotics
-
Moons T, de Roo M, Claes S, and Dom G (2011) Relationship between P-glycoprotein and second-generation antipsychotics. Pharmacogenomics 12:1193-1211.
-
(2011)
Pharmacogenomics
, vol.12
, pp. 1193-1211
-
-
Moons, T.1
De Roo, M.2
Claes, S.3
Dom, G.4
-
28
-
-
0034763005
-
Rational use of in vitro P-glycoprotein assays in drug discovery
-
Polli JW, Wring SA, Humphreys JE, Huang L, Morgan JB, Webster LO, and Serabjit-Singh CS (2001) Rational use of in vitro P-glycoprotein assays in drug discovery. J Pharmacol Exp Ther 299:620-628. (Pubitemid 32979675)
-
(2001)
Journal of Pharmacology and Experimental Therapeutics
, vol.299
, Issue.2
, pp. 620-628
-
-
Polli, J.W.1
Wring, S.A.2
Humphreys, J.E.3
Huang, L.4
Morgan, J.B.5
Webster, L.O.6
Serabjit-Singh, C.S.7
-
30
-
-
84880654833
-
In vitro characterization of axitinib interactions with human efflux and hepatic uptake transporters: Implications for disposition and drug interactions
-
Reyner EL, Sevidal S, West MA, Clouser-Roche A, Freiwald S, Fenner K, Ullah M, Lee CA, and Smith BJ (2013) In vitro characterization of axitinib interactions with human efflux and hepatic uptake transporters: implications for disposition and drug interactions. Drug Metab Dispos 41:1575-1583.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 1575-1583
-
-
Reyner, E.L.1
Sevidal, S.2
West, M.A.3
Clouser-Roche, A.4
Freiwald, S.5
Fenner, K.6
Ullah, M.7
Lee, C.A.8
Smith, B.J.9
-
31
-
-
78650811745
-
Effects of multiple doses of ambrisentan on the pharmacokinetics of a single dose of digoxin in healthy volunteers
-
Richards DB, Spence R, Mandagere A, Henderson LS, and Magee MH (2011) Effects of multiple doses of ambrisentan on the pharmacokinetics of a single dose of digoxin in healthy volunteers. J Clin Pharmacol 51:102-106.
-
(2011)
J Clin Pharmacol
, vol.51
, pp. 102-106
-
-
Richards, D.B.1
Spence, R.2
Mandagere, A.3
Henderson, L.S.4
Magee, M.H.5
-
32
-
-
79952709519
-
pROC: An open-source package for R and S+ to analyze and compare ROC curves
-
Robin X, Turck N, Hainard A, Tiberti N, Lisacek F, Sanchez JC, and Müller M (2011) pROC: an open-source package for R and S+ to analyze and compare ROC curves. BMC Bioinformatics 12:77-84.
-
(2011)
BMC Bioinformatics
, vol.12
, pp. 77-84
-
-
Robin, X.1
Turck, N.2
Hainard, A.3
Tiberti, N.4
Lisacek, F.5
Sanchez, J.C.6
Müller, M.7
-
33
-
-
0037464458
-
Comparison of in vitro P-glycoprotein screening assays: Recommendations for their use in drug discovery
-
DOI 10.1021/jm021012t
-
Schwab D, Fischer H, Tabatabaei A, Poli S, and Huwyler J (2003) Comparison of in vitro P-glycoprotein screening assays: recommendations for their use in drug discovery. J Med Chem 46:1716-1725. (Pubitemid 36444224)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.9
, pp. 1716-1725
-
-
Schwab, D.1
Fischer, H.2
Tabatabaei, A.3
Poli, S.4
Huwyler, J.5
-
34
-
-
0032518454
-
A general pattern for substrate recognition by P-glycoprotein
-
Seelig A (1998) A general pattern for substrate recognition by P-glycoprotein. Eur J Biochem 251:252-261.
-
(1998)
Eur J Biochem
, vol.251
, pp. 252-261
-
-
Seelig, A.1
-
35
-
-
84906864410
-
Ocular delivery screening scheme for systemically administered ophthalmic drugs
-
Abstract
-
Singh SK, Shawer M, Andrus PK, Raub TJ, and Vrbanac JJ (2003) Ocular delivery screening scheme for systemically administered ophthalmic drugs (Abstract). Invest Ophthalmol Vis Sci 44:4426.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 4426
-
-
Singh, S.K.1
Shawer, M.2
Andrus, P.K.3
Raub, T.J.4
Vrbanac, J.J.5
-
36
-
-
0035108539
-
Grapefruit juice enhances intestinal absorption of the P-glycoprotein substrate talinolol
-
DOI 10.1016/S0928-0987(00)00191-3, PII S0928098700001913
-
Spahn-Langguth H and Langguth P (2001) Grapefruit juice enhances intestinal absorption of the P-glycoprotein substrate talinolol. Eur J Pharm Sci 12:361-367. (Pubitemid 32166734)
-
(2001)
European Journal of Pharmaceutical Sciences
, vol.12
, Issue.4
, pp. 361-367
-
-
Spahn-Langguth, H.1
Langguth, P.2
-
37
-
-
84875851139
-
Retrospective analysis of P-glycoprotein-mediated drug-drug interactions at the blood-brain barrier in humans
-
Sugimoto H, Hirabayashi H, Amano N, and Moriwaki T (2013) Retrospective analysis of P-glycoprotein-mediated drug-drug interactions at the blood-brain barrier in humans. Drug Metab Dispos 41:683-688.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 683-688
-
-
Sugimoto, H.1
Hirabayashi, H.2
Amano, N.3
Moriwaki, T.4
-
38
-
-
78650747680
-
Quantitative investigation of the impact of P-glycoprotein inhibition on drug transport across bloodbrain barrier in rats
-
Sugimoto H, Hirabayashi H, Kimura Y, Furuta A, Amano N, and Moriwaki T (2011a) Quantitative investigation of the impact of P-glycoprotein inhibition on drug transport across bloodbrain barrier in rats. Drug Metab Dispos 39:8-14.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 8-14
-
-
Sugimoto, H.1
Hirabayashi, H.2
Kimura, Y.3
Furuta, A.4
Amano, N.5
Moriwaki, T.6
-
39
-
-
79960150931
-
Establishment of in vitro P-glycoprotein inhibition assay and its exclusion criteria to assess the risk of drug-drug interaction at the drug discovery stage
-
Sugimoto H, Matsumoto S, Tachibana M, Niwa S, Hirabayashi H, Amano N, and Moriwaki T (2011b) Establishment of in vitro P-glycoprotein inhibition assay and its exclusion criteria to assess the risk of drug-drug interaction at the drug discovery stage. J Pharm Sci 100:4013-4023.
-
(2011)
J Pharm Sci
, vol.100
, pp. 4013-4023
-
-
Sugimoto, H.1
Matsumoto, S.2
Tachibana, M.3
Niwa, S.4
Hirabayashi, H.5
Amano, N.6
Moriwaki, T.7
-
40
-
-
34250744722
-
Central nervous system drug disposition: The relationship between in situ brain permeability and brain free fraction
-
DOI 10.1124/jpet.107.121525
-
Summerfield SG, Read K, Begley DJ, Obradovic T, Hidalgo IJ, Coggon S, Lewis AV, Porter RA, and Jeffrey P (2007) Central nervous system drug disposition: the relationship between in situ brain permeability and brain free fraction. J Pharmacol Exp Ther 322:205-213. (Pubitemid 46956363)
-
(2007)
Journal of Pharmacology and Experimental Therapeutics
, vol.322
, Issue.1
, pp. 205-213
-
-
Summerfield, S.G.1
Read, K.2
Begley, D.J.3
Obradovic, T.4
Hidalgo, I.J.5
Coggon, S.6
Lewis, A.V.7
Porter, R.A.8
Jeffrey, P.9
-
41
-
-
69249202502
-
Method for predicting the risk of drug-drug interactions involving inhibition of intestinal CYP3A4 and P-glycoprotein
-
Tachibana T, Kato M, Watanabe T, Mitsui T, and Sugiyama Y (2009) Method for predicting the risk of drug-drug interactions involving inhibition of intestinal CYP3A4 and P-glycoprotein. Xenobiotica 39:430-443.
-
(2009)
Xenobiotica
, vol.39
, pp. 430-443
-
-
Tachibana, T.1
Kato, M.2
Watanabe, T.3
Mitsui, T.4
Sugiyama, Y.5
-
42
-
-
0023447098
-
Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues
-
Thiebaut F, Tsuruo T, Hamada H, Gottesman MM, Pastan I, and Willingham MC (1987) Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. Proc Natl Acad Sci USA 84:7735-7738.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 7735-7738
-
-
Thiebaut, F.1
Tsuruo, T.2
Hamada, H.3
Gottesman, M.M.4
Pastan, I.5
Willingham, M.C.6
-
43
-
-
84879417173
-
Transporter studies in drug development: Experience to date and follow-up on decision trees from the International Transporter Consortium
-
International Transporter Consortium
-
Tweedie D, Polli JW, Berglund EG, Huang SM, Zhang L, Poirier A, Chu X, and Feng B; International Transporter Consortium (2013) Transporter studies in drug development: experience to date and follow-up on decision trees from the International Transporter Consortium. Clin Pharmacol Ther 94:113-125.
-
(2013)
Clin Pharmacol Ther
, vol.94
, pp. 113-125
-
-
Tweedie, D.1
Polli, J.W.2
Berglund, E.G.3
Huang, S.M.4
Zhang, L.5
Poirier, A.6
Chu, X.7
Feng, B.8
-
44
-
-
0036206856
-
Interaction of morphine, fentanyl, sufentanil, alfentanil, and loperamide with the efflux drug transporter P-glycoprotein
-
DOI 10.1097/00000542-200204000-00019
-
Wandel C, Kim R, Wood M, and Wood A (2002) Interaction of morphine, fentanyl, sufentanil, alfentanil, and loperamide with the efflux drug transporter P-glycoprotein. Anesthesiology 96:913-920. (Pubitemid 34266685)
-
(2002)
Anesthesiology
, vol.96
, Issue.4
, pp. 913-920
-
-
Wandel, C.1
Kim, R.2
Wood, M.3
Wood, A.4
-
45
-
-
84860783554
-
Exploiting transport activity of p-glycoprotein at the blood-brain barrier for the development of peripheral cannabinoid type 1 receptor antagonists
-
Wittgen HG, Greupink R, van den Heuvel JJ, van den Broek PH, Dinter-Heidorn H, Koenderink JB, and Russel FG (2012) Exploiting transport activity of p-glycoprotein at the blood-brain barrier for the development of peripheral cannabinoid type 1 receptor antagonists. Mol Pharm 9:1351-1360.
-
(2012)
Mol Pharm
, vol.9
, pp. 1351-1360
-
-
Wittgen, H.G.1
Greupink, R.2
Van Den Heuvel, J.J.3
Van Den Broek, P.H.4
Dinter-Heidorn, H.5
Koenderink, J.B.6
Russel, F.G.7
-
46
-
-
48749084803
-
A regulatory viewpoint on transporter-based drug interactions
-
Zhang L, Zhang YD, Strong JM, Reynolds KS, and Huang SM (2008) A regulatory viewpoint on transporter-based drug interactions. Xenobiotica 38:709-724.
-
(2008)
Xenobiotica
, vol.38
, pp. 709-724
-
-
Zhang, L.1
Zhang, Y.D.2
Strong, J.M.3
Reynolds, K.S.4
Huang, S.M.5
-
47
-
-
0035054725
-
The gut as a barrier to drug absorption: Combined role of cytochrome P450 3A and P-glycoprotein
-
Zhang Y and Benet LZ (2001) The gut as a barrier to drug absorption: combined role of cytochrome P450 3A and P-glycoprotein. Clin Pharmacokinet 40:159-168. (Pubitemid 32324448)
-
(2001)
Clinical Pharmacokinetics
, vol.40
, Issue.3
, pp. 159-168
-
-
Zhang, Y.1
Benet, L.Z.2
|