-
1
-
-
0037407596
-
A role for Pglycoprotein in environmental toxicology
-
Abu-Quare, A. W., Elmasry, E., and Abou-Donia, M. B. 2003. A role for Pglycoprotein in environmental toxicology. J. Toxicol. Environ. Health B 6:279-288.
-
(2003)
J. Toxicol. Environ. Health B
, vol.6
, pp. 279-288
-
-
Abu-Quare, A.W.1
Elmasry, E.2
Abou-Donia, M.B.3
-
2
-
-
3543039989
-
Efficacy of novel P-glycoprotein inhibitors to increase the oral uptake of paclitaxel in mice
-
Bardelmeijer, H. A., Ouwehand, M., Beijnen, J. H., Schellens, J. H. M., and van Tellingen, O. 2004. Efficacy of novel P-glycoprotein inhibitors to increase the oral uptake of paclitaxel in mice. Invest. New Drugs 22:219-229.
-
(2004)
Invest. New Drugs
, vol.22
, pp. 219-229
-
-
Bardelmeijer, H.A.1
Ouwehand, M.2
Beijnen, J.H.3
Schellens, J.H.M.4
van Tellingen, O.5
-
3
-
-
0028970047
-
Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9
-
Baldwin, S. J., Bloomer, J. C., Smith, G. J., Ayrton, A. D., Clarke, S. E., and Chenery, R. J. 1995. Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9. Xenobiotica 25:261-270.
-
(1995)
Xenobiotica
, vol.25
, pp. 261-270
-
-
Baldwin, S.J.1
Bloomer, J.C.2
Smith, G.J.3
Ayrton, A.D.4
Clarke, S.E.5
Chenery, R.J.6
-
4
-
-
0035157254
-
A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry
-
Dierks, E. A., Stams, K. R., Lim, H. K., Cornelius, G., Zhang, H., and Ball, S. E. 2001. A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry. Drug Metab. Dispos. 29:23-29.
-
(2001)
Drug Metab. Dispos
, vol.29
, pp. 23-29
-
-
Dierks, E.A.1
Stams, K.R.2
Lim, H.K.3
Cornelius, G.4
Zhang, H.5
Ball, S.E.6
-
5
-
-
0029939665
-
Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemosensitizers
-
Ford, J. M., 1996. Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemosensitizers. Eur. J. Cancer 32A:991-1001.
-
(1996)
Eur. J. Cancer
, vol.32 A
, pp. 991-1001
-
-
Ford, J.M.1
-
6
-
-
8444251671
-
Phase I study of docetaxel in combination with the P-glycoprotein inhibitor, zosuquidar, in resistant malignancies
-
Fracasso, P. M., Goldstein, L. J., de Alwis, D. P., Rader, J. S., Arquette, M. A., Goodner, S. A., Wright, L. P., Fears, C. L., Gazak, R. J., Andre, V. A. M., Burgess, M. F., Slapak, C. A., and Schellens, J. H. M. 2004. Phase I study of docetaxel in combination with the P-glycoprotein inhibitor, zosuquidar, in resistant malignancies. Clin. Cancer Res. 10:7220-7228.
-
(2004)
Clin. Cancer Res
, vol.10
, pp. 7220-7228
-
-
Fracasso, P.M.1
Goldstein, L.J.2
de Alwis, D.P.3
Rader, J.S.4
Arquette, M.A.5
Goodner, S.A.6
Wright, L.P.7
Fears, C.L.8
Gazak, R.J.9
Andre, V.A.M.10
Burgess, M.F.11
Slapak, C.A.12
Schellens, J.H.M.13
-
7
-
-
0036364467
-
Multidrug resistance in cancer: Role of ATP-dependent transporters
-
Gottesman, M. M., Fojo, T., and Bates, S. E. 2002. Multidrug resistance in cancer: Role of ATP-dependent transporters. Natl. Rev. Cancer 2:48-58.
-
(2002)
Natl. Rev. Cancer
, vol.2
, pp. 48-58
-
-
Gottesman, M.M.1
Fojo, T.2
Bates, S.E.3
-
8
-
-
0030012182
-
Chlorpyrifos oxon interacts with the mammalian multidrug resistance protein, P-glycoprotein
-
Lanning, C. L., Fine, R. L., Sachs, C. W., Rao, U. S., Corcoran, J. J., and Abou-Donia, M. B. 1996. Chlorpyrifos oxon interacts with the mammalian multidrug resistance protein, P-glycoprotein. J. Toxicol. Environ. Health 47:395-407.
-
(1996)
J. Toxicol. Environ. Health
, vol.47
, pp. 395-407
-
-
Lanning, C.L.1
Fine, R.L.2
Sachs, C.W.3
Rao, U.S.4
Corcoran, J.J.5
Abou-Donia, M.B.6
-
9
-
-
0034231606
-
P-glycoprotein as a drug target in the treatment of multidrug resistant cancer
-
Lehne, G. 2000. P-glycoprotein as a drug target in the treatment of multidrug resistant cancer. Curr. Drug Targets 1:85-99.
-
(2000)
Curr. Drug Targets
, vol.1
, pp. 85-99
-
-
Lehne, G.1
-
10
-
-
0344765487
-
Characterization of the selectivity and mechanism of human cytochrome P450 inhibition by the human immunodeficiency virus-protease inhibitor nelfinavir mesylate
-
Lillibridge, J. H., Liang, B. H., Kerr, B. M., Webber, S., Quart, B., Shetty, B., and Lee, C. A. 1998. Characterization of the selectivity and mechanism of human cytochrome P450 inhibition by the human immunodeficiency virus-protease inhibitor nelfinavir mesylate. Drug Metab. Dispos. 26:609-616.
-
(1998)
Drug Metab. Dispos
, vol.26
, pp. 609-616
-
-
Lillibridge, J.H.1
Liang, B.H.2
Kerr, B.M.3
Webber, S.4
Quart, B.5
Shetty, B.6
Lee, C.A.7
-
11
-
-
0028858960
-
Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
-
Newton, D. J., Wang, R. W., and Lu, A. Y. 1995. Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab. Dispos. 23:154-158.
-
(1995)
Drug Metab. Dispos
, vol.23
, pp. 154-158
-
-
Newton, D.J.1
Wang, R.W.2
Lu, A.Y.3
-
12
-
-
33645731196
-
Simultaneous determination of paclitaxel and a new P-glycoprotein inhibitor HM-30181 in rat plasma by liquid chromatography with tandem mass spectrometry
-
Paek, I. B., Ji, H. Y., Kim, M. S., Lee, K. S., and Lee, H. S. 2006a. Simultaneous determination of paclitaxel and a new P-glycoprotein inhibitor HM-30181 in rat plasma by liquid chromatography with tandem mass spectrometry. J. Sep. Sci. 29:628-634.
-
(2006)
J. Sep. Sci
, vol.29
, pp. 628-634
-
-
Paek, I.B.1
Ji, H.Y.2
Kim, M.S.3
Lee, K.S.4
Lee, H.S.5
-
13
-
-
33646229094
-
Metabolism of a new P-glycoprotein inhibitor HM-30181 in rats using liquid chromatography/electrospray mass spectrometry
-
Paek, I. B., Ji, H. Y., Kim, M. S., Lee, K. S., and Lee, H. S. 2006b. Metabolism of a new P-glycoprotein inhibitor HM-30181 in rats using liquid chromatography/electrospray mass spectrometry. Rapid Comm. Mass Spectrom. 20:1457-1462.
-
(2006)
Rapid Comm. Mass Spectrom
, vol.20
, pp. 1457-1462
-
-
Paek, I.B.1
Ji, H.Y.2
Kim, M.S.3
Lee, K.S.4
Lee, H.S.5
-
14
-
-
23644452472
-
Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma
-
Pusztai, L., Wagner, P., Ibrahim, N., Rivera, E., Theriault, R., Booser, D., Symmans, F.W., Wong, F., Blumenschein, G., Fleming, D. R., Rouzier, R., Boniface, G., and Hortobagyi, G. N. 2005. Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma. Cancer 104:682-691.
-
(2005)
Cancer
, vol.104
, pp. 682-691
-
-
Pusztai, L.1
Wagner, P.2
Ibrahim, N.3
Rivera, E.4
Theriault, R.5
Booser, D.6
Symmans, F.W.7
Wong, F.8
Blumenschein, G.9
Fleming, D.R.10
Rouzier, R.11
Boniface, G.12
Hortobagyi, G.N.13
-
15
-
-
0027136660
-
Clinical trials of agents that reverse multidrug resistance. A literature review
-
Raderer, M. and Scheithauer, W. 1993. Clinical trials of agents that reverse multidrug resistance. A literature review. Cancer 72:3553-3563.
-
(1993)
Cancer
, vol.72
, pp. 3553-3563
-
-
Raderer, M.1
Scheithauer, W.2
-
16
-
-
0036810537
-
Multidrug resistance in ovarian cancer: Comparing an immunocytochemical study and ATP-tumor chemosensitivity assay
-
Raspollini, M. R., Pinzani, P., Pazzagli, M., Baroni, G., Taddei, A., Amunni, G., Villanucci, A., and Taddei, G. L. 2002. Multidrug resistance in ovarian cancer: comparing an immunocytochemical study and ATP-tumor chemosensitivity assay. J. Chemother. 14:518-525.
-
(2002)
J. Chemother
, vol.14
, pp. 518-525
-
-
Raspollini, M.R.1
Pinzani, P.2
Pazzagli, M.3
Baroni, G.4
Taddei, A.5
Amunni, G.6
Villanucci, A.7
Taddei, G.L.8
-
17
-
-
11844283327
-
Inhibition of human CYP2B6 by N,N′,N″-triethylenethiophosphoramide is irreversible and mechanism-based
-
Richter, T., Schwab, M., Eichelbaum, M., and Znager, U. M. 2005. Inhibition of human CYP2B6 by N,N′,N″-triethylenethiophosphoramide is irreversible and mechanism-based. Biochem. Pharmacol. 69:517-524.
-
(2005)
Biochem. Pharmacol
, vol.69
, pp. 517-524
-
-
Richter, T.1
Schwab, M.2
Eichelbaum, M.3
Znager, U.M.4
-
18
-
-
2542479863
-
A phase I trial of a potent P-glycoprotein inhibitor, zosuquidar trihydrochloride (LY335979), administered intravenously in combination with doxorubicin in patients with advanced malignancy
-
Sandler, A., Gordon, M., de Alwis D. P., Pouliquen, I., Green, L., Marder, P., Chaudhary, A., Fife, K., Battiato, L., Sweeney, C., Jordan, C., Burgess, M., and Slapak, C. A. 2004. A phase I trial of a potent P-glycoprotein inhibitor, zosuquidar trihydrochloride (LY335979), administered intravenously in combination with doxorubicin in patients with advanced malignancy. Clin. Cancer Res. 10:3265-3272.
-
(2004)
Clin. Cancer Res
, vol.10
, pp. 3265-3272
-
-
Sandler, A.1
Gordon, M.2
de Alwis, D.P.3
Pouliquen, I.4
Green, L.5
Marder, P.6
Chaudhary, A.7
Fife, K.8
Battiato, L.9
Sweeney, C.10
Jordan, C.11
Burgess, M.12
Slapak, C.A.13
-
19
-
-
0025294782
-
Furafylline is a potent and selective inhibitor of cytochrme P450IA2 in man
-
Sesardic, D., Boobis, A. R., Murray, B. P., Murray, S., Segura, J., de la Torre, R., and Davies, D. S. 1990. Furafylline is a potent and selective inhibitor of cytochrme P450IA2 in man. Br. J. Clin. Pharmacol. 29:651-663.
-
(1990)
Br. J. Clin. Pharmacol
, vol.29
, pp. 651-663
-
-
Sesardic, D.1
Boobis, A.R.2
Murray, B.P.3
Murray, S.4
Segura, J.5
de la Torre, R.6
Davies, D.S.7
-
20
-
-
0028237729
-
Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
-
Shimada, T., Yamazaki, H., Mimura, M., Inui, Y., and Guengerich, F. P. 1994. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J. Pharmacol. Exp. Ther. 270:414-423.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.270
, pp. 414-423
-
-
Shimada, T.1
Yamazaki, H.2
Mimura, M.3
Inui, Y.4
Guengerich, F.P.5
-
21
-
-
0031436164
-
Pharmacologic approaches to reversing multidrug resistance
-
Sikic, B. I. 1997. Pharmacologic approaches to reversing multidrug resistance. Semin. Hematol. 34(4 suppl. 5):40-47.
-
(1997)
Semin. Hematol
, vol.34
, Issue.4 SUPPL. 5
, pp. 40-47
-
-
Sikic, B.I.1
-
22
-
-
0034496578
-
Does P-glycoprotein play a role in anticancer drug pharmacokinetics?
-
Sparreboom, A., and Nooter, K. 2000. Does P-glycoprotein play a role in anticancer drug pharmacokinetics? Drug Resist. Update 3:357-363.
-
(2000)
Drug Resist. Update
, vol.3
, pp. 357-363
-
-
Sparreboom, A.1
Nooter, K.2
-
23
-
-
0036179579
-
+)-N-3-Benzylnirvanol and (-)-N-3-benzyl-phenobarbital: New potent and selective in vitro inhibitors of CYP2C19
-
Suzuki, H., Kneller, M. B., Haining, R. L., Trager, W. F., and Rettie, A. E. 2002. (+)-N-3-Benzylnirvanol and (-)-N-3-benzyl-phenobarbital: New potent and selective in vitro inhibitors of CYP2C19. Drug Metab. Dispos. 30:235-239.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 235-239
-
-
Suzuki, H.1
Kneller, M.B.2
Haining, R.L.3
Trager, W.F.4
Rettie, A.E.5
-
24
-
-
0037358040
-
Overcoming multidrug resistance in cancer: An update on the clinical strategy of inhibiting P-glycoprotein
-
Thomas, H., and Coley, H. M. 2003. Overcoming multidrug resistance in cancer: an update on the clinical strategy of inhibiting P-glycoprotein. Cancer Control 10:159-165.
-
(2003)
Cancer Control
, vol.10
, pp. 159-165
-
-
Thomas, H.1
Coley, H.M.2
-
25
-
-
0029743080
-
Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents
-
von Moltke, L. L., Greenblatt, D. J., Schmider, J., Duan, S. X., Wright, C. E., Harmatz, J. S., and Shader, R. I. 1996. Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents. J. Clin. Pharmacol. 36:783-791.
-
(1996)
J. Clin. Pharmacol
, vol.36
, pp. 783-791
-
-
von Moltke, L.L.1
Greenblatt, D.J.2
Schmider, J.3
Duan, S.X.4
Wright, C.E.5
Harmatz, J.S.6
Shader, R.I.7
-
26
-
-
0031931102
-
Protease inhibitors as inhibitors of human cytochromes P450: High risk associated with ritonavir
-
von Moltke, L. L., Greenblatt, D. J., Grassi, J. M., Granda, B. W., Duan, S. X., Fogelman, S. M., Daily, J. P., Harmatz, J. S., and Shader, R. I. 1998. Protease inhibitors as inhibitors of human cytochromes P450: High risk associated with ritonavir. J. Clin. Pharmacol. 38:106-111.
-
(1998)
J. Clin. Pharmacol
, vol.38
, pp. 106-111
-
-
von Moltke, L.L.1
Greenblatt, D.J.2
Grassi, J.M.3
Granda, B.W.4
Duan, S.X.5
Fogelman, S.M.6
Daily, J.P.7
Harmatz, J.S.8
Shader, R.I.9
-
27
-
-
1242338943
-
Inhibition of P-glycoprotein function by XR-9576 in a solid tumor model can restore anticancer drug efficacy
-
Walker, J., Martin, C., and Callaghan, R. 2004. Inhibition of P-glycoprotein function by XR-9576 in a solid tumor model can restore anticancer drug efficacy. Eur. J. Cancer 40:594-605.
-
(2004)
Eur. J. Cancer
, vol.40
, pp. 594-605
-
-
Walker, J.1
Martin, C.2
Callaghan, R.3
-
28
-
-
14044254791
-
Selective inhibition of human cytochrome P4502C8 by montelukast
-
Walsky, R. L., Obach, R. S., Gaman, E. A., Gleeson, J. P. R., and Protor, W. R. 2005. Selective inhibition of human cytochrome P4502C8 by montelukast. Drug Metab. Dispos. 33:413-418.
-
(2005)
Drug Metab. Dispos
, vol.33
, pp. 413-418
-
-
Walsky, R.L.1
Obach, R.S.2
Gaman, E.A.3
Gleeson, J.P.R.4
Protor, W.R.5
-
29
-
-
0032859247
-
Midazolam α-hydroxylation by human liver microsomes in vitro: Inhibition by calcium channel blockers, itraconazole and ketoconazole
-
Wang, J. S., Wen, X., Backman, J. T., Taavitsainen, P., Neubonnen, P. J., and Kivisto, K. T. 1999. Midazolam α-hydroxylation by human liver microsomes in vitro: Inhibition by calcium channel blockers, itraconazole and ketoconazole. Pharmacol. Toxicol. 85:157-161.
-
(1999)
Pharmacol. Toxicol
, vol.85
, pp. 157-161
-
-
Wang, J.S.1
Wen, X.2
Backman, J.T.3
Taavitsainen, P.4
Neubonnen, P.J.5
Kivisto, K.T.6
-
30
-
-
0041301863
-
Identification of an inducible form of cytochrome P-450 in human liver
-
Watkins, P. B., Wrighton, S. A., Mauel, P., Schuets, E. G., Mendezpicon, G., Parker, G. A., and Guzelian, P. S. 1985. Identification of an inducible form of cytochrome P-450 in human liver. Proc. Nat. Acad. Sci. USA 82:6310-6314.
-
(1985)
Proc. Nat. Acad. Sci. USA
, vol.82
, pp. 6310-6314
-
-
Watkins, P.B.1
Wrighton, S.A.2
Mauel, P.3
Schuets, E.G.4
Mendezpicon, G.5
Parker, G.A.6
Guzelian, P.S.7
-
31
-
-
0025161416
-
Studies on the expression and metabolic capabilities of human liver cytochrome P-450 IIIA4 (HLp 3)
-
Wrighton, S. A., Brian, W. R., Sari, M. A., Iwasaki, M., Guengerich, F. P., Raucy, J. L., Molowa, D. T., and Vandenbranden, M. 1990. Studies on the expression and metabolic capabilities of human liver cytochrome P-450 IIIA4 (HLp 3). Mol. Pharmacol. 38:207-213.
-
(1990)
Mol. Pharmacol
, vol.38
, pp. 207-213
-
-
Wrighton, S.A.1
Brian, W.R.2
Sari, M.A.3
Iwasaki, M.4
Guengerich, F.P.5
Raucy, J.L.6
Molowa, D.T.7
Vandenbranden, M.8
-
32
-
-
34547227034
-
-
Wrighton, S. A., and Thummel, K. E. 2000. CYP3A. In Metabolic drug interactions, eds. R. H. Levy, K. E. Thummel, W. F. Trager, P. D. Hansten, and M. Eichelbaum pp. 115-133. Philadelphia: Lippincott Williams & Wilkins.
-
Wrighton, S. A., and Thummel, K. E. 2000. CYP3A. In Metabolic drug interactions, eds. R. H. Levy, K. E. Thummel, W. F. Trager, P. D. Hansten, and M. Eichelbaum pp. 115-133. Philadelphia: Lippincott Williams & Wilkins.
-
-
-
-
33
-
-
0025841777
-
Purification and characterization of human liver microsomal cytochrome P450 2A6
-
Yun, C. H., Shimada, T., and Guengerich, F. P. 1991. Purification and characterization of human liver microsomal cytochrome P450 2A6. Mol. Pharmacol. 40:679-685.
-
(1991)
Mol. Pharmacol
, vol.40
, pp. 679-685
-
-
Yun, C.H.1
Shimada, T.2
Guengerich, F.P.3
|