-
1
-
-
0030004763
-
Cooperative, competitive and noncompetitive interactions between modulators of P-glycoprotein
-
Ayesh S, Shao YM, and Stein WD (1996) Cooperative, competitive and noncompetitive interactions between modulators of P-glycoprotein. Biochim Biophys Acta 1316:8-18.
-
(1996)
Biochim Biophys Acta
, vol.1316
, pp. 8-18
-
-
Ayesh, S.1
Shao, Y.M.2
Stein, W.D.3
-
2
-
-
0014767029
-
Cellular resistance to actinomycin D in chinese hamster cells in vitro: Cross-resistance, radioautographic and cytogenetic studies
-
Biedler JL and Riehm H (1970) Cellular resistance to actinomycin D in chinese hamster cells in vitro: Cross-resistance, radioautographic and cytogenetic studies. Cancer Res 30:1174-1184.
-
(1970)
Cancer Res
, vol.30
, pp. 1174-1184
-
-
Biedler, J.L.1
Riehm, H.2
-
3
-
-
0030069428
-
Reversible labeling of a chemosensitizer binding domain of P-glycoprotein with a novel 1,4-dihydropyridine drug transport inhibitor
-
Boer R, Dichtl M, Borchers C, Ulrich WR, Marecek JF, Prestwich GD, Glossmann H, and Striessnig J (1996) Reversible labeling of a chemosensitizer binding domain of P-glycoprotein with a novel 1,4-dihydropyridine drug transport inhibitor. Biochemistry 35:1387-1396.
-
(1996)
Biochemistry
, vol.35
, pp. 1387-1396
-
-
Boer, R.1
Dichtl, M.2
Borchers, C.3
Ulrich, W.R.4
Marecek, J.F.5
Prestwich, G.D.6
Glossmann, H.7
Striessnig, J.8
-
4
-
-
0030062653
-
Competition of hydrophobic peptides, cytotoxic drugs and chemosensitizers on a common P-glycoprotein pharmacophore as revealed by its ATPase activity
-
Borgnia MJ, Eytan GD, and Assaraf YG (1996) Competition of hydrophobic peptides, cytotoxic drugs and chemosensitizers on a common P-glycoprotein pharmacophore as revealed by its ATPase activity. J Biol Chem 271:3163-3171.
-
(1996)
J Biol Chem
, vol.271
, pp. 3163-3171
-
-
Borgnia, M.J.1
Eytan, G.D.2
Assaraf, Y.G.3
-
5
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254.
-
(1976)
Anal Biochem
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
6
-
-
0344761958
-
The importance of a nitrogene atom in modulators of multidrug resistance
-
Ecker G, Huber M, Schmid D, and Chiba P (1999) The importance of a nitrogene atom in modulators of multidrug resistance. Mol Pharmacol 56:791-796.
-
(1999)
Mol Pharmacol
, vol.56
, pp. 791-796
-
-
Ecker, G.1
Huber, M.2
Schmid, D.3
Chiba, P.4
-
7
-
-
18344364851
-
Application of three-dimentional quantitative structure-activity relationships of P-glycoprotein inhibitors and substrates
-
Ekins S, Kim RB, Leake BF, Dantzig AH, Schuetz EG, Lan L-B, Yasuda K, Shepard RL, Winter MA, Schuetz JD, et al. (2002a) Application of three-dimentional quantitative structure-activity relationships of P-glycoprotein inhibitors and substrates. Mol Pharmacol 61:974-981.
-
(2002)
Mol Pharmacol
, vol.61
, pp. 974-981
-
-
Ekins, S.1
Kim, R.B.2
Leake, B.F.3
Dantzig, A.H.4
Schuetz, E.G.5
Lan, L.-B.6
Yasuda, K.7
Shepard, R.L.8
Winter, M.A.9
Schuetz, J.D.10
-
8
-
-
18344390872
-
Three-dimentional quantitative structure-activity relationships of inhibitors of P-glycoprotein
-
Ekins S, Kim RB, Leake BF, Dantzig AH, Schuetz EG, Lan L-B, Yasuda K, Shepard RL, Winter MA, Schuetz JD, et al. (2002b) Three-dimentional quantitative structure-activity relationships of inhibitors of P-glycoprotein. Mol Pharmacol 61:964-973.
-
(2002)
Mol Pharmacol
, vol.61
, pp. 964-973
-
-
Ekins, S.1
Kim, R.B.2
Leake, B.F.3
Dantzig, A.H.4
Schuetz, E.G.5
Lan, L.-B.6
Yasuda, K.7
Shepard, R.L.8
Winter, M.A.9
Schuetz, J.D.10
-
10
-
-
0033969525
-
Analysis of the tangled relationships between P-glycoproteinmediated multidrug resistance and the lipid phase of the cell membrane
-
Ferté J (2000) Analysis of the tangled relationships between P-glycoproteinmediated multidrug resistance and the lipid phase of the cell membrane. Eur J Biochem 267:277-294.
-
(2000)
Eur J Biochem
, vol.267
, pp. 277-294
-
-
Ferté, J.1
-
11
-
-
0024432823
-
Identification of the multidrug resistance-related P-glycoprotein as a cyclosporine binding protein
-
Foxwell BM, Mackie A, Ling V, and Ryffel B (1989) Identification of the multidrug resistance-related P-glycoprotein as a cyclosporine binding protein. Mol Pharmacol 36:543-546.
-
(1989)
Mol Pharmacol
, vol.36
, pp. 543-546
-
-
Foxwell, B.M.1
Mackie, A.2
Ling, V.3
Ryffel, B.4
-
12
-
-
0027484689
-
Absence of cooperativity for MgATP and verapamil effects on the ATPase activity of P-glycoprotein containing membrane vesicles
-
Garrigos M, Belehradek J Jr, Mir LM, and Orlowski S (1993) Absence of cooperativity for MgATP and verapamil effects on the ATPase activity of P-glycoprotein containing membrane vesicles. Biochem Biophys Res Commun 196:1034-1041.
-
(1993)
Biochem Biophys Res Commun
, vol.196
, pp. 1034-1041
-
-
Garrigos, M.1
Belehradek J., Jr.2
Mir, L.M.3
Orlowski, S.4
-
13
-
-
0031039693
-
Competitive and non-competitive inhibition of the multidrug-resistance-associated P-glycoprotein ATPase: Further experimental evidence for a multisite model
-
Garrigos M, Mir LM, and Orlowski S (1997) Competitive and non-competitive inhibition of the multidrug-resistance-associated P-glycoprotein ATPase: Further experimental evidence for a multisite model. Eur J Biochem 244:664-673.
-
(1997)
Eur J Biochem
, vol.244
, pp. 664-673
-
-
Garrigos, M.1
Mir, L.M.2
Orlowski, S.3
-
14
-
-
0026155124
-
Backbone cyclization: A new method for conferring conformational constraint on peptides
-
Gilon C, Halle D, Chorev M, Selinger Z, and Byk G (1991) Backbone cyclization: A new method for conferring conformational constraint on peptides. Biopolymers 31:745-750.
-
(1991)
Biopolymers
, vol.31
, pp. 745-750
-
-
Gilon, C.1
Halle, D.2
Chorev, M.3
Selinger, Z.4
Byk, G.5
-
15
-
-
0027218689
-
Biochemistry of multidrug resistance by the multidrug transporter
-
Gottesman MM and Pastan I (1993) Biochemistry of multidrug resistance by the multidrug transporter. Annu Rev Biochem 62:385-427.
-
(1993)
Annu Rev Biochem
, vol.62
, pp. 385-427
-
-
Gottesman, M.M.1
Pastan, I.2
-
16
-
-
0033710983
-
Microdialysis study of bromocriptine and its metabolites in rat pituitary and striatum
-
Granveau-Renouf S, Valente D, Durocher A, Grognet JM, and Ezan E (2000) Microdialysis study of bromocriptine and its metabolites in rat pituitary and striatum. Eur J Drug Metab Pharmacokinet 25:79-84.
-
(2000)
Eur J Drug Metab Pharmacokinet
, vol.25
, pp. 79-84
-
-
Granveau-Renouf, S.1
Valente, D.2
Durocher, A.3
Grognet, J.M.4
Ezan, E.5
-
17
-
-
0030800078
-
Quantitative structure-activity relationship of multidrug resistance reversal agents
-
Klopman G, Shi LM, and Ramu A (1997) Quantitative structure-activity relationship of multidrug resistance reversal agents. Mol Pharmacol 52:323-334.
-
(1997)
Mol Pharmacol
, vol.52
, pp. 323-334
-
-
Klopman, G.1
Shi, L.M.2
Ramu, A.3
-
18
-
-
0030743356
-
Competitive, noncompetitive and cooperative interactions between substrates of P-glycoprotein as measured by its ATPase activity
-
Litman T, Zeuthen T, Skovsgaard T, and Stein WD (1997a) Competitive, noncompetitive and cooperative interactions between substrates of P-glycoprotein as measured by its ATPase activity. Biochim Biophys Acta 1361:169-176.
-
(1997)
Biochim Biophys Acta
, vol.1361
, pp. 169-176
-
-
Litman, T.1
Zeuthen, T.2
Skovsgaard, T.3
Stein, W.D.4
-
19
-
-
0030791978
-
Structure-activity relationships of P-glycoprotein interacting drugs: Kinetic characterization of their effects on ATPase activity
-
Litman T, Zeuthen T, Skovsgaard T, and Stein WD (1997b) Structure-activity relationships of P-glycoprotein interacting drugs: Kinetic characterization of their effects on ATPase activity. Biochim Biophys Acta 1361:159-168.
-
(1997)
Biochim Biophys Acta
, vol.1361
, pp. 159-168
-
-
Litman, T.1
Zeuthen, T.2
Skovsgaard, T.3
Stein, W.D.4
-
20
-
-
0033862765
-
Communication between multiple drug binding sites on P-glycoprotein
-
Martin C, Berridge G, Higgins CF, Mistry P, Charlton P, and Callaghan R (2000) Communication between multiple drug binding sites on P-glycoprotein. Mol Pharmacol 58:624-632.
-
(2000)
Mol Pharmacol
, vol.58
, pp. 624-632
-
-
Martin, C.1
Berridge, G.2
Higgins, C.F.3
Mistry, P.4
Charlton, P.5
Callaghan, R.6
-
21
-
-
0026597449
-
Simple method of calculation octanol/water partition coefficient
-
Moriguchi I, Hirono S, Liu Q, Nakagome I, and Matsushita Y (1992) Simple method of calculation octanol/water partition coefficient. Chem Pharm Bull 40:127-139.
-
(1992)
Chem Pharm Bull
, vol.40
, pp. 127-139
-
-
Moriguchi, I.1
Hirono, S.2
Liu, Q.3
Nakagome, I.4
Matsushita, Y.5
-
22
-
-
0024584440
-
Competitive inhibition by verapamil of ATP-dependent high affinity vincristine binding to the plasma membrane of multidrug-resistant K562 cells without calcium ion involvement
-
Naito M and Tsuruo T (1989) Competitive inhibition by verapamil of ATP-dependent high affinity vincristine binding to the plasma membrane of multidrug-resistant K562 cells without calcium ion involvement. Cancer Res 49:1452-1455.
-
(1989)
Cancer Res
, vol.49
, pp. 1452-1455
-
-
Naito, M.1
Tsuruo, T.2
-
23
-
-
0033404139
-
Multiple recognition of various amphiphilic molecules by the multidrug resistance P-glycoprotein: Molecular mechanisms and pharmacological consequences coming from functional interactions between various drugs
-
Orlowski S and Garrigos M (1999) Multiple recognition of various amphiphilic molecules by the multidrug resistance P-glycoprotein: Molecular mechanisms and pharmacological consequences coming from functional interactions between various drugs. Anticancer Res 19:3109-3124.
-
(1999)
Anticancer Res
, vol.19
, pp. 3109-3124
-
-
Orlowski, S.1
Garrigos, M.2
-
24
-
-
0030035535
-
Effects of steroids and verapamil on P-glycoprotein ATPase activity: Progesterone, desoxycorticosterone, corticosterone and verapamil are mutually non-exclusive modulators
-
Orlowski S, Mir LM, Belehradek J Jr, and Garrigos M (1996) Effects of steroids and verapamil on P-glycoprotein ATPase activity: Progesterone, desoxycorticosterone, corticosterone and verapamil are mutually non-exclusive modulators. Biochem J 317:515-522.
-
(1996)
Biochem J
, vol.317
, pp. 515-522
-
-
Orlowski, S.1
Mir, L.M.2
Belehradek J., Jr.3
Garrigos, M.4
-
26
-
-
0034077338
-
Theoretical calculation and prediction of Pglycoprotein-interacting drugs using MolSurf parametrization and PLS statistics
-
Osterberg T and Norinder U (2000) Theoretical calculation and prediction of Pglycoprotein-interacting drugs using MolSurf parametrization and PLS statistics. Eur J Pharmaceut Sci 10:295-303.
-
(2000)
Eur J Pharmaceut Sci
, vol.10
, pp. 295-303
-
-
Osterberg, T.1
Norinder, U.2
-
27
-
-
0032528254
-
Multidrug resistance transporter P-glycoprotein has distinct but interacting binding sites for cytotoxic drugs and reversing agents
-
Pascaud C, Garrigos M, and Orlowski S (1998) Multidrug resistance transporter P-glycoprotein has distinct but interacting binding sites for cytotoxic drugs and reversing agents. Biochem J 333:351-358.
-
(1998)
Biochem J
, vol.333
, pp. 351-358
-
-
Pascaud, C.1
Garrigos, M.2
Orlowski, S.3
-
29
-
-
0029033361
-
Multiple interconverting conformers of the cyclic tetrapeptide tentoxin, [cyclo-(L-MeAla1-L-Leu2-MePhe[(Z) delta]3-Gly4)], as seen by two-dimensional 1H-nmr spectroscopy
-
Pinet E, Neumann JM, Dahse I, Girault G, and André F (1995) Multiple interconverting conformers of the cyclic tetrapeptide tentoxin, [cyclo-(L-MeAla1-L-Leu2-MePhe[(Z) delta]3-Gly4)], as seen by two-dimensional 1H-nmr spectroscopy. Biopolymers 36:135-152.
-
(1995)
Biopolymers
, vol.36
, pp. 135-152
-
-
Pinet, E.1
Neumann, J.M.2
Dahse, I.3
Girault, G.4
André, F.5
-
30
-
-
0028217326
-
Direct demonstration of high affinity interactions of immunosuppressant drugs with the drug binding site of the human P-glycoprotein
-
Rao US and Scarborough GA (1994) Direct demonstration of high affinity interactions of immunosuppressant drugs with the drug binding site of the human P-glycoprotein. Mol Pharmacol 45:773-776.
-
(1994)
Mol Pharmacol
, vol.45
, pp. 773-776
-
-
Rao, U.S.1
Scarborough, G.A.2
-
31
-
-
0027418815
-
Human P-glycoprotein transports cyclosporin A and FK506
-
Saeki T, Ueda K, Tanigawara Y, Hori R, and Komano T (1993) Human P-glycoprotein transports cyclosporin A and FK506. J Biol Chem 268:6077-6080.
-
(1993)
J Biol Chem
, vol.268
, pp. 6077-6080
-
-
Saeki, T.1
Ueda, K.2
Tanigawara, Y.3
Hori, R.4
Komano, T.5
-
32
-
-
0000622931
-
Photoaffinity labeling of the multidrug-resistance-related P-glycoprotein with photoactive analogs of verapamil
-
Safa AR (1988) Photoaffinity labeling of the multidrug-resistance-related P-glycoprotein with photoactive analogs of verapamil. Proc Natl Acad Sci USA 85:7187-7191.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 7187-7191
-
-
Safa, A.R.1
-
34
-
-
0031158805
-
The physiological function of drug-transporting P-glycoproteins
-
Schinkel AH (1997) The physiological function of drug-transporting P-glycoproteins. Semin Cancer Biol 8:161-170.
-
(1997)
Semin Cancer Biol
, vol.8
, pp. 161-170
-
-
Schinkel, A.H.1
-
35
-
-
0029892497
-
P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs
-
Schinkel AH, Wagenaar E, Mol CAAM, and van Deemter L (1996) P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs. J Clin Investig 97:2517-2524.
-
(1996)
J Clin Investig
, vol.97
, pp. 2517-2524
-
-
Schinkel, A.H.1
Wagenaar, E.2
Mol, C.A.A.M.3
Van Deemter, L.4
-
36
-
-
0032822237
-
Structure-activity relationship studies of propafenone analogs based on P-glycoprotein ATPase activity measurements
-
Schmid D, Ecker G, Kopp S, Hitzler M, and Chiba P (1999) Structure-activity relationship studies of propafenone analogs based on P-glycoprotein ATPase activity measurements. Biochem Pharmacol 58:1447-1456.
-
(1999)
Biochem Pharmacol
, vol.58
, pp. 1447-1456
-
-
Schmid, D.1
Ecker, G.2
Kopp, S.3
Hitzler, M.4
Chiba, P.5
-
37
-
-
0035824388
-
Structural mechanisms of QacR induction and multidrug recognition
-
Schumacher MA, Miller MC, Grkovic S, Brown MH, Skurray RA, and Brennan RG (2001) Structural mechanisms of QacR induction and multidrug recognition. Science (Wash DC) 294:2158-2163.
-
(2001)
Science (Wash DC)
, vol.294
, pp. 2158-2163
-
-
Schumacher, M.A.1
Miller, M.C.2
Grkovic, S.3
Brown, M.H.4
Skurray, R.A.5
Brennan, R.G.6
-
38
-
-
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
-
39
-
-
0033083015
-
Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone: Evidence for a third drug-binding site
-
Shapiro AB, Fox K, Lam P, and Ling V (1999) Stimulation of P-glycoprotein-mediated drug transport by prazosin and progesterone: Evidence for a third drug-binding site. Eur J Biochem 259:841-850.
-
(1999)
Eur J Biochem
, vol.259
, pp. 841-850
-
-
Shapiro, A.B.1
Fox, K.2
Lam, P.3
Ling, V.4
-
40
-
-
0030782511
-
Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities
-
Shapiro AB and Ling V (1997) Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities. Eur J Biochem 250:130-137.
-
(1997)
Eur J Biochem
, vol.250
, pp. 130-137
-
-
Shapiro, A.B.1
Ling, V.2
-
41
-
-
0029987548
-
Synthetic hydrophobic peptides are substrates for P-glycoprotein and stimulate drug transport
-
Sharom FJ, Yu X, Di Diodato G, and Chu JWK (1996) Synthetic hydrophobic peptides are substrates for P-glycoprotein and stimulate drug transport. Biochem J 320:421-428.
-
(1996)
Biochem J
, vol.320
, pp. 421-428
-
-
Sharom, F.J.1
Yu, X.2
Di Diodato, G.3
Chu, J.W.K.4
-
42
-
-
0032530441
-
Effect of modulators on the ATPase activity and vanadate nucleotide trapping of human P-glycoprotein
-
Shepard RL, Winter MA, Hsaio SC, Pearce HL, Beck WT, and Dantzig AH (1998) Effect of modulators on the ATPase activity and vanadate nucleotide trapping of human P-glycoprotein. Biochem Pharmacol 56:719-727.
-
(1998)
Biochem Pharmacol
, vol.56
, pp. 719-727
-
-
Shepard, R.L.1
Winter, M.A.2
Hsaio, S.C.3
Pearce, H.L.4
Beck, W.T.5
Dantzig, A.H.6
-
43
-
-
0030966409
-
Kinetics of the multidrug transporter (P-glycoprotein) and its reversal
-
Stein WD (1997) Kinetics of the multidrug transporter (P-glycoprotein) and its reversal. Physiol Rev 77:545-590.
-
(1997)
Physiol Rev
, vol.77
, pp. 545-590
-
-
Stein, W.D.1
-
44
-
-
0025991731
-
Azidopine noncompetitively interacts with vinblastine and cyclosporin A binding to P-glycoprotein in multidrug resistant cells
-
Tamai I and Safa AR (1991) Azidopine noncompetitively interacts with vinblastine and cyclosporin A binding to P-glycoprotein in multidrug resistant cells. J Biol Chem 266:16796-16800.
-
(1991)
J Biol Chem
, vol.266
, pp. 16796-16800
-
-
Tamai, I.1
Safa, A.R.2
-
45
-
-
0023224665
-
Cyclosporin A and its analogues as modifiers of adriamycin and vincristine resistance in a multi-drug resistant human lung cancer cell line
-
Twentyman PR, Fox NE, and White DJG (1987) Cyclosporin A and its analogues as modifiers of adriamycin and vincristine resistance in a multi-drug resistant human lung cancer cell line. Br J Cancer 56:55-57.
-
(1987)
Br J Cancer
, vol.56
, pp. 55-57
-
-
Twentyman, P.R.1
Fox, N.E.2
White, D.J.G.3
-
46
-
-
0034739274
-
Two transport binding sites of P-glycoprotein are unequal yet contingent: Initial rate kinetic analysis by ATP hydrolysis demonstrates intersite dependence
-
Wang E, Casciano CN, Clement RP, and Johnson WW (2000) Two transport binding sites of P-glycoprotein are unequal yet contingent: Initial rate kinetic analysis by ATP hydrolysis demonstrates intersite dependence. Biochim Biophys Acta 1481: 63-74.
-
(2000)
Biochim Biophys Acta
, vol.1481
, pp. 63-74
-
-
Wang, E.1
Casciano, C.N.2
Clement, R.P.3
Johnson, W.W.4
-
47
-
-
0035047222
-
Structure-activity relationships of multidrug resistance reversers
-
Wiese M and Pajeva IK (2001) Structure-activity relationships of multidrug resistance reversers. Curr Med Chem 8:685-713.
-
(2001)
Curr Med Chem
, vol.8
, pp. 685-713
-
-
Wiese, M.1
Pajeva, I.K.2
-
48
-
-
0023898749
-
Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells
-
Zamora JM, Pearce HL, and Beck WT (1988) Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells. Mol Pharmacol 33:454-462.
-
(1988)
Mol Pharmacol
, vol.33
, pp. 454-462
-
-
Zamora, J.M.1
Pearce, H.L.2
Beck, W.T.3
|