-
1
-
-
0003586906
-
-
Oxford University Press, Oxford
-
Pratt, W. B., R. W. Ruddon, W. D. Ensminger, and J. Maybaum. The Anticancer Drugs. Oxford University Press, Oxford (1994).
-
(1994)
The Anticancer Drugs
-
-
Pratt, W.B.1
Ruddon, R.W.2
Ensminger, W.D.3
Maybaum, J.4
-
2
-
-
0014767029
-
Cellular resistance to actinomycin D in Chinese hamster cells in vitro: Cross-resistance, radioautographic, and cytogenetic studies
-
Biedler, J. L., and H. Riehm. Cellular resistance to actinomycin D in Chinese hamster cells in vitro: cross-resistance, radioautographic, and cytogenetic studies. Cancer Res. 30:1174-1184 (1970).
-
(1970)
Cancer Res.
, vol.30
, pp. 1174-1184
-
-
Biedler, J.L.1
Riehm, H.2
-
3
-
-
0028935166
-
Modulators of multidrug resistance - Preclinical studies
-
Ford, J. M. Modulators of multidrug resistance - preclinical studies. Hematol. Oncol. Clin. N. Am. 9:337-361 (1995).
-
(1995)
Hematol. Oncol. Clin. N. Am.
, vol.9
, pp. 337-361
-
-
Ford, J.M.1
-
4
-
-
0026683638
-
P-glycoprotein as a multidrug transporter: A critical review of current multidrug resistant cell lines
-
Nielsen, D., and T. Skovsgaard. P-glycoprotein as a multidrug transporter: a critical review of current multidrug resistant cell lines. Biochim. Biophy. Acta 1139:169-183 (1992).
-
(1992)
Biochim. Biophy. Acta
, vol.1139
, pp. 169-183
-
-
Nielsen, D.1
Skovsgaard, T.2
-
5
-
-
33645830172
-
A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants
-
Juliano, R. L., and V. Ling. A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochim. Biophy. Acta 455:152-162 (1976).
-
(1976)
Biochim. Biophy. Acta
, vol.455
, pp. 152-162
-
-
Juliano, R.L.1
Ling, V.2
-
6
-
-
0018566696
-
Purification of P-glycoprotein from plasma membrane vesicles of Chinese hamster ovary cell mutants with reduced colchicine permeability
-
Riordan, J. R., and V. Ling. Purification of P-glycoprotein from plasma membrane vesicles of Chinese hamster ovary cell mutants with reduced colchicine permeability. J. Biol. Chem. 254:12701-12705 (1979).
-
(1979)
J. Biol. Chem.
, vol.254
, pp. 12701-12705
-
-
Riordan, J.R.1
Ling, V.2
-
7
-
-
0022972654
-
Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cells
-
Chen, C.-j., J. E. Chin, K. Ueda, D. P. Clark, I. Pastan, M. M. Gottesman, and I. B. Roninson. Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cells. Cell 47:381-389 (1986).
-
(1986)
Cell
, vol.47
, pp. 381-389
-
-
Chen, C.-J.1
Chin, J.E.2
Ueda, K.3
Clark, D.P.4
Pastan, I.5
Gottesman, M.M.6
Roninson, I.B.7
-
8
-
-
0027218689
-
Biochemistry of multidrug resistance mediated by the multidrug transporter
-
Gottesman, M. M., and I. Pastan. Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu. Rev. Biochem. 62:385-427 (1993).
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 385-427
-
-
Gottesman, M.M.1
Pastan, I.2
-
9
-
-
0027484339
-
Multidrug Resistance: Clinical relevance in acute leukemia
-
List, A. F. Multidrug Resistance: clinical relevance in acute leukemia. Oncology 7:23-28, 32, 35-38 (1993).
-
(1993)
Oncology
, vol.7
, pp. 23-28
-
-
List, A.F.1
-
10
-
-
0023898749
-
Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells
-
Zamora, J. M., H. L. Pearce, and W. T. Beck. Physical-chemical properties shared by compounds that modulate multidrug resistance in human leukemic cells. Mol. Pharmacol. 33:454-462 (1988).
-
(1988)
Mol. Pharmacol.
, vol.33
, pp. 454-462
-
-
Zamora, J.M.1
Pearce, H.L.2
Beck, W.T.3
-
11
-
-
0027315937
-
Resistance to lipophilic cationic compounds in multidrug resistant leukemia cells
-
Ramu, A., and N. Ramu. Resistance to lipophilic cationic compounds in multidrug resistant leukemia cells. Leuk. Lymphoma 9:247-253 (1993).
-
(1993)
Leuk. Lymphoma
, vol.9
, pp. 247-253
-
-
Ramu, A.1
Ramu, N.2
-
12
-
-
0026354420
-
New potent verapamil derivatives that reverse multidrug resistance in human renal carcinoma cells and in transgenic mice expressing the human MDRl gene
-
Mickisch, G. H., G. T. Merlino, P. M. Aiken, M. M. Gottesman, and I. Pastan. New potent verapamil derivatives that reverse multidrug resistance in human renal carcinoma cells and in transgenic mice expressing the human MDRl gene. J. Urol. 146:447-453 (1991).
-
(1991)
J. Urol.
, vol.146
, pp. 447-453
-
-
Mickisch, G.H.1
Merlino, G.T.2
Aiken, P.M.3
Gottesman, M.M.4
Pastan, I.5
-
13
-
-
0028063849
-
Characteristics of P388/VMDRC.04, a simple, sensitive model for studying P-glycoprotein antagonists
-
Yang, J. M., S. Goldenberg, M. M. Gottesman, and W. N. Hait. Characteristics of P388/VMDRC.04, a simple, sensitive model for studying P-glycoprotein antagonists. Cancer Res. 54:730-737 (1994).
-
(1994)
Cancer Res.
, vol.54
, pp. 730-737
-
-
Yang, J.M.1
Goldenberg, S.2
Gottesman, M.M.3
Hait, W.N.4
-
14
-
-
0027455618
-
Reversal of P-glycoprotein-associated multidrug resistance: The challenge continues
-
Lehnert, M. Reversal of P-glycoprotein-associated multidrug resistance: the challenge continues. Eur. J. Cancer 29A:636-638 (1993).
-
(1993)
Eur. J. Cancer
, vol.29 A
, pp. 636-638
-
-
Lehnert, M.1
-
15
-
-
0028923624
-
Clinical studies with modulators of multidrug resistance
-
Fisher, G. A., and B. I. Sikic. Clinical studies with modulators of multidrug resistance. Hematol. Oncol. Clin. N. Am. 9:363-382 (1995).
-
(1995)
Hematol. Oncol. Clin. N. Am.
, vol.9
, pp. 363-382
-
-
Fisher, G.A.1
Sikic, B.I.2
-
16
-
-
0028816350
-
A phase III randomized study of oral verapamil as a chemosensitizer to reverse drug resistance in patients with refractory myeloma: A Southwest oncology group study
-
Dalton, W. S., J. J. Crowley, S. S. Salmon, T. M. Grogan, L. R. Laufman, G. R. Weiss, and J. D. Bonnet. A phase III randomized study of oral verapamil as a chemosensitizer to reverse drug resistance in patients with refractory myeloma: a Southwest oncology group study. Cancer (Phila.) 75:815-820 (1995).
-
(1995)
Cancer (Phila.)
, vol.75
, pp. 815-820
-
-
Dalton, W.S.1
Crowley, J.J.2
Salmon, S.S.3
Grogan, T.M.4
Laufman, L.R.5
Weiss, G.R.6
Bonnet, J.D.7
-
17
-
-
0026512425
-
Rational design and pre-clinical pharmacology of drugs for reversing multidrug resistance
-
Hait, W. N., and D. T. Aftab. Rational design and pre-clinical pharmacology of drugs for reversing multidrug resistance. Biochem. Pharmacol. 43:103-107 (1992).
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 103-107
-
-
Hait, W.N.1
Aftab, D.T.2
-
18
-
-
0027892892
-
Design and tumor targeting of anthracyclines able to overcome multidrug resistance: A double-advantage approach
-
Priebe, W., and R. Perez-Soler. Design and tumor targeting of anthracyclines able to overcome multidrug resistance: a double-advantage approach. Pharmacol Ther. 60:215-234 (1993).
-
(1993)
Pharmacol Ther.
, vol.60
, pp. 215-234
-
-
Priebe, W.1
Perez-Soler, R.2
-
19
-
-
0028030228
-
Rhodamine efflux patterns predict P-glycoprotein substrates in the National Cancer Institute drug screen
-
Lee, J. S., K. Paull, M. Alvarez, C. Hose, A. Monks, M. Grever, A. T. Fojo, and S. E. Bates. Rhodamine efflux patterns predict P-glycoprotein substrates in the National Cancer Institute drug screen. Mol. Pharmacol. 46:627-638 (1994).
-
(1994)
Mol. Pharmacol.
, vol.46
, pp. 627-638
-
-
Lee, J.S.1
Paull, K.2
Alvarez, M.3
Hose, C.4
Monks, A.5
Grever, M.6
Fojo, A.T.7
Bates, S.E.8
-
20
-
-
0024312538
-
Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
-
Paull, K. D., R. H. Shoemaker, L. Hodes, A. Monks, D. A. Scudiero, L. Rubinstein, J. Plowman, and M. R. Boyd. Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithm. J. Natl. Cancer Inst. 81:1088-1092 (1989).
-
(1989)
J. Natl. Cancer Inst.
, vol.81
, pp. 1088-1092
-
-
Paull, K.D.1
Shoemaker, R.H.2
Hodes, L.3
Monks, A.4
Scudiero, D.A.5
Rubinstein, L.6
Plowman, J.7
Boyd, M.R.8
-
21
-
-
0026442149
-
Structural requirements of simple organic cations for recognition by multidrug resistant cells
-
Dellinger, M., B. C. Pressman, C. Calderon-Higginson, N. Savaraj, H. Tapiero, D. Kolonias, and T. J. Lampidis. Structural requirements of simple organic cations for recognition by multidrug resistant cells. Cancer Res. 52:6385-6389 (1992).
-
(1992)
Cancer Res.
, vol.52
, pp. 6385-6389
-
-
Dellinger, M.1
Pressman, B.C.2
Calderon-Higginson, C.3
Savaraj, N.4
Tapiero, H.5
Kolonias, D.6
Lampidis, T.J.7
-
22
-
-
0027743492
-
The role of drug-lipid interactions in the biological activity of modulators of multi-drug resistance
-
Wadkins, R. M., and P. J. Houghton. The role of drug-lipid interactions in the biological activity of modulators of multi-drug resistance. Biochim. Biophys. Acta 1153:225-236 (1993).
-
(1993)
Biochim. Biophys. Acta
, vol.1153
, pp. 225-236
-
-
Wadkins, R.M.1
Houghton, P.J.2
-
23
-
-
0028224534
-
Cell biological mechanisms of multidrug resistance in tumors
-
Simon, S. M., and M. Schindler. Cell biological mechanisms of multidrug resistance in tumors. Proc. Natl. Acad. Sci. USA 91:3497-3504 (1994).
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 3497-3504
-
-
Simon, S.M.1
Schindler, M.2
-
24
-
-
0026730489
-
Structure-based strategies for drug design and discovery
-
Kuntz, I. D. Structure-based strategies for drug design and discovery. Science (Washington D. C.) 257:1078-1082 (1992).
-
(1992)
Science (Washington D. C.)
, vol.257
, pp. 1078-1082
-
-
Kuntz, I.D.1
-
25
-
-
0026778110
-
MULTICASE. A hierarchical computer automated structure evaluation program
-
Klopman, G. MULTICASE. A hierarchical computer automated structure evaluation program. Quant. Struct.-Act. Relat. 11:176-184 (1992).
-
(1992)
Quant. Struct.-Act. Relat.
, vol.11
, pp. 176-184
-
-
Klopman, G.1
-
26
-
-
0026739494
-
Structure-activity study, and design of multidrug-resistant reversal compounds by a computer automated structure evaluation methodology
-
Klopman, G., S. Srivastava, I. Kolossvary, R. F. Epand, N. Ahmed, and R. M. Epand. Structure-activity study, and design of multidrug-resistant reversal compounds by a computer automated structure evaluation methodology. Cancer Res. 52:4121-4129 (1992).
-
(1992)
Cancer Res.
, vol.52
, pp. 4121-4129
-
-
Klopman, G.1
Srivastava, S.2
Kolossvary, I.3
Epand, R.F.4
Ahmed, N.5
Epand, R.M.6
-
27
-
-
0026624915
-
Reversal of multidrug resistance by phenothiazines and structurally related compounds
-
Ramu, A., and N. Ramu. Reversal of multidrug resistance by phenothiazines and structurally related compounds. Cancer Chemother. Pharmacol. 30:165-173 (1992).
-
(1992)
Cancer Chemother. Pharmacol.
, vol.30
, pp. 165-173
-
-
Ramu, A.1
Ramu, N.2
-
28
-
-
0028107822
-
Reversal of multidrug resistance by bis(phenylalkyl)amines and structurally related compounds
-
Ramu, A., and N. Ramu. Reversal of multidrug resistance by bis(phenylalkyl)amines and structurally related compounds. Cancer Chemother. Pharmacol. 34:423-430 (1994).
-
(1994)
Cancer Chemother. Pharmacol.
, vol.34
, pp. 423-430
-
-
Ramu, A.1
Ramu, N.2
-
29
-
-
0028106003
-
Diversity of multidrug resistance in mammalian cells
-
Devine, S. E., and P. Melera. Diversity of multidrug resistance in mammalian cells. J. Biol. Chem. 269:6133-6139 (1994).
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 6133-6139
-
-
Devine, S.E.1
Melera, P.2
-
30
-
-
0003143478
-
Chapter 5. Modulation of P-glycoprotein-mediated multidrug resistance
-
CRC Press, Boca Raton, FL
-
Tew, K. D., P. J. Houghton, and J. A. Houghton. Chapter 5. Modulation of P-glycoprotein-mediated multidrug resistance, in Preclinical and Clinical Modulation of Anticancer Drugs. CRC Press, Boca Raton, FL, 125-196 (1993).
-
(1993)
Preclinical and Clinical Modulation of Anticancer Drugs
, pp. 125-196
-
-
Tew, K.D.1
Houghton, P.J.2
Houghton, J.A.3
-
31
-
-
0027155036
-
Reversal of multidrug resistance by a new lipophilic cationic molecule, S9788. Comparison with 11 other MDR-modulating agents in a model of doxorubicin-resistant rat glioblastoma cells
-
Huet, S., C. Chapey, and J. Robert. Reversal of multidrug resistance by a new lipophilic cationic molecule, S9788. Comparison with 11 other MDR-modulating agents in a model of doxorubicin-resistant rat glioblastoma cells. Eur. J. Cancer 29A:1377-1383 (1993).
-
(1993)
Eur. J. Cancer
, vol.29 A
, pp. 1377-1383
-
-
Huet, S.1
Chapey, C.2
Robert, J.3
-
32
-
-
0024507079
-
Circumvention of adriamycin resistance by dipyridamole analogues: A structure-activity relationship study
-
Ramu, N., and A. Ramu. Circumvention of adriamycin resistance by dipyridamole analogues: a structure-activity relationship study. Intl. J. Cancer 43:487-491 (1989).
-
(1989)
Intl. J. Cancer
, vol.43
, pp. 487-491
-
-
Ramu, N.1
Ramu, A.2
-
33
-
-
0001848065
-
Computer simulation of physical chemical properties of organic molecules
-
Klopman, G., and M. McGonigal. Computer simulation of physical chemical properties of organic molecules. J. Chem. Inf. Comput. Sci. 21:48-52 (1981).
-
(1981)
J. Chem. Inf. Comput. Sci.
, vol.21
, pp. 48-52
-
-
Klopman, G.1
McGonigal, M.2
-
34
-
-
0021529312
-
Artificial intelligence approach to structure-activity studies. Computer automated structure evaluation of biological activity of organic molecules
-
Klopman, G. Artificial intelligence approach to structure-activity studies. Computer automated structure evaluation of biological activity of organic molecules. J. Am. Chem. Soc. 106:7315-7320 (1984).
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 7315-7320
-
-
Klopman, G.1
-
35
-
-
0024260626
-
Weakly polar interactions in proteins
-
Burley, S. K., and G. A. Petsko. Weakly polar interactions in proteins. Adv. Protein Chem. 39:125-189 (1988).
-
(1988)
Adv. Protein Chem.
, vol.39
, pp. 125-189
-
-
Burley, S.K.1
Petsko, G.A.2
-
36
-
-
0028097634
-
Transmembrane aromatic amino acid distribution in P-glycoprotein: A functional role in broad substrate specificity
-
Pawagi, A. B., J. Wang, M. Silverman, R. A. F. Reithmeier, and C. M. Deber. Transmembrane aromatic amino acid distribution in P-glycoprotein: a functional role in broad substrate specificity. J. Mol. Biol. 235:554-564 (1994).
-
(1994)
J. Mol. Biol.
, vol.235
, pp. 554-564
-
-
Pawagi, A.B.1
Wang, J.2
Silverman, M.3
Reithmeier, R.A.F.4
Deber, C.M.5
-
37
-
-
0001843250
-
Taxane anticancer agents. Basic science and current status
-
Georg, G. I., T. T. Chen, I. Ojima, and D. M. Vyas. Taxane anticancer agents. Basic science and current status. ACS Symp. Ser. 583:1-353 (1995).
-
(1995)
ACS Symp. Ser.
, vol.583
, pp. 1-353
-
-
Georg, G.I.1
Chen, T.T.2
Ojima, I.3
Vyas, D.M.4
-
38
-
-
0028713237
-
Use of extreme drug resistance assay to evaluate mechanisms of resistance in ovarian cancer: Taxol resistance and MDR1 expression
-
Fruehauf, J. P., and A. Manetta. Use of extreme drug resistance assay to evaluate mechanisms of resistance in ovarian cancer: Taxol resistance and MDR1 expression. Contrib. Gynecol. Obstet. 19:39-52 (1994).
-
(1994)
Contrib. Gynecol. Obstet.
, vol.19
, pp. 39-52
-
-
Fruehauf, J.P.1
Manetta, A.2
-
39
-
-
0027791809
-
In vitro evaluation of chemosensitizers for clinical reversal of P-glycoprotein-associated Taxol resistance
-
Lehnert, M., S. Emerson, W. S. Dalton, R. de Giuli, and S. E. Salmon. In vitro evaluation of chemosensitizers for clinical reversal of P-glycoprotein-associated Taxol resistance. Monogr. Natl. Cancer Inst. 15:63-67 (1993).
-
(1993)
Monogr. Natl. Cancer Inst.
, vol.15
, pp. 63-67
-
-
Lehnert, M.1
Emerson, S.2
Dalton, W.S.3
De Giuli, R.4
Salmon, S.E.5
-
40
-
-
0027303904
-
The nitrogen of the acetamido group of colchicine modulates P-glycoprotein-mediated multidrug resistance
-
Tang-Wai, D. F., A. Brossi, L. D. Arnold, and P. Gros. The nitrogen of the acetamido group of colchicine modulates P-glycoprotein-mediated multidrug resistance. Biochemistry 32:6470-6476 (1993).
-
(1993)
Biochemistry
, vol.32
, pp. 6470-6476
-
-
Tang-Wai, D.F.1
Brossi, A.2
Arnold, L.D.3
Gros, P.4
-
41
-
-
0000887546
-
Essential features of the P-glycoprotein pharmacophore as denned by a series of reserpine analogs that modulate multidrug resistance
-
Pearce, H. L., A. L. Safa, N. J. Bach, M. A. Winter, M. C. Cirtain, and W. T. Beck. Essential features of the P-glycoprotein pharmacophore as denned by a series of reserpine analogs that modulate multidrug resistance. Proc. Natl. Acad. Sci. USA 86:5128-5132 (1989).
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 5128-5132
-
-
Pearce, H.L.1
Safa, A.L.2
Bach, N.J.3
Winter, M.A.4
Cirtain, M.C.5
Beck, W.T.6
-
42
-
-
0025059269
-
Structural characteristics of compounds that modulate P-glycoprotein-associated multidrug resistance
-
Pearce, H. L., M. A. Winter, and W. T. Beck. Structural characteristics of compounds that modulate P-glycoprotein-associated multidrug resistance. Adv. Enzyme Regul. 30:357-373 (1990).
-
(1990)
Adv. Enzyme Regul.
, vol.30
, pp. 357-373
-
-
Pearce, H.L.1
Winter, M.A.2
Beck, W.T.3
-
43
-
-
0023926589
-
Reversal of resistance to vincristine in P388 leukemia by various polycyclic clinical drugs, with a special emphasis on quinacrine
-
Inaba, M., and E. Maruyama. Reversal of resistance to vincristine in P388 leukemia by various polycyclic clinical drugs, with a special emphasis on quinacrine. Cancer Res. 48:2064-2067 (1988).
-
(1988)
Cancer Res.
, vol.48
, pp. 2064-2067
-
-
Inaba, M.1
Maruyama, E.2
-
44
-
-
0025328006
-
Reversal of multidrug resistance by lipophilic drugs
-
Hofsli, E., and J. Nissen-Meyer. Reversal of multidrug resistance by lipophilic drugs. Cancer Res. 50:3997-4002 (1990).
-
(1990)
Cancer Res.
, vol.50
, pp. 3997-4002
-
-
Hofsli, E.1
Nissen-Meyer, J.2
-
45
-
-
0024806599
-
Reversal by Cefoperazone of resistance to etoposide, doxorubicin, and vinblastine in multidrug resistant human sarcoma cells
-
Gosland, M. P., B. L. Lum, and B. I. Sikic. Reversal by Cefoperazone of resistance to etoposide, doxorubicin, and vinblastine in multidrug resistant human sarcoma cells. Cancer Res. 49:6901-6905 (1989).
-
(1989)
Cancer Res.
, vol.49
, pp. 6901-6905
-
-
Gosland, M.P.1
Lum, B.L.2
Sikic, B.I.3
-
46
-
-
0024595844
-
Analysis of structural features of dihydropyride analogs needed to reverse multidrug resistance and to inhibit photoaffinity labeling of P-glycoprotein
-
Nogae, I. K., Kohno, J. Kikuchi, M. Kuwano, S. Akiyama, A. Kiue, K. Suzuki, Y. Yoshida, M. M. Cornwell, I. Pastan, and M. M. Gottesman. Analysis of structural features of dihydropyride analogs needed to reverse multidrug resistance and to inhibit photoaffinity labeling of P-glycoprotein. Biochem. Pharmacol. 38:519-527 (1989).
-
(1989)
Biochem. Pharmacol.
, vol.38
, pp. 519-527
-
-
Nogae, I.K.1
Kohno2
Kikuchi, J.3
Kuwano, M.4
Akiyama, S.5
Kiue, A.6
Suzuki, K.7
Yoshida, Y.8
Cornwell, M.M.9
Pastan, I.10
Gottesman, M.M.11
-
47
-
-
0024365293
-
3H]azidopine photolabeling of P-glycoprotein by newly synthesized dihydropyridine analogues in a human cell line
-
3H]azidopine photolabeling of P-glycoprotein by newly synthesized dihydropyridine analogues in a human cell line. Cancer Res. 49:3190-3195 (1989).
-
(1989)
Cancer Res.
, vol.49
, pp. 3190-3195
-
-
Kamiwatari, M.1
Nagata, Y.2
Kikuchi, H.3
Yoshimura, A.4
Sumizawa, T.5
Shudo, N.6
Sakoda, R.7
Seto, K.8
Akiyama, A.9
-
48
-
-
0025059014
-
Activities of newly synthesized dihydropyridines in overcoming of vincristine resistance, calcium antagonism, and inhibition of photoaffinity labeling of P-glycoprotein in rodents
-
Kiue, A., T. Sano, K. Suzuki, H. Inada, M. Okumura, J. Kikuchi, S. Sato, K. Kohno, and M. Kuwano. Activities of newly synthesized dihydropyridines in overcoming of vincristine resistance, calcium antagonism, and inhibition of photoaffinity labeling of P-glycoprotein in rodents. Cancer Res. 50:310-317 (1990).
-
(1990)
Cancer Res.
, vol.50
, pp. 310-317
-
-
Kiue, A.1
Sano, T.2
Suzuki, K.3
Inada, H.4
Okumura, M.5
Kikuchi, J.6
Sato, S.7
Kohno, K.8
Kuwano, M.9
-
49
-
-
0024534226
-
Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance
-
Ford, J. M., W. C. Prozialeck, and W. N. Hait. Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance. Mol. Pharmacol. 35:105-115 (1989).
-
(1989)
Mol. Pharmacol.
, vol.35
, pp. 105-115
-
-
Ford, J.M.1
Prozialeck, W.C.2
Hait, W.N.3
-
50
-
-
0025267821
-
Cellular and biochemical characterization of thioxanthenes for reversal of multidrug resistance in human and murine cell lines
-
Ford, J. M., E. P. Bruggemann, I. Pastan, M. M. Gottesman, and W. N. Hait. Cellular and biochemical characterization of thioxanthenes for reversal of multidrug resistance in human and murine cell lines. Cancer Res. 50: 1748-1756 (1990).
-
(1990)
Cancer Res.
, vol.50
, pp. 1748-1756
-
-
Ford, J.M.1
Bruggemann, E.P.2
Pastan, I.3
Gottesman, M.M.4
Hait, W.N.5
-
51
-
-
0025084766
-
Structural determinants of phenoxazine type compounds required to modulate the accumulation of vinblastine and vincristine in multidrug-resistant cell lines
-
Thimmaiah, K. N., J. K. Horton, X. D. Qian, W. T. Beck, J. A. Houghton, and P. J. Houghton. Structural determinants of phenoxazine type compounds required to modulate the accumulation of vinblastine and vincristine in multidrug-resistant cell lines. Cancer Commun. 2:249-259 (1990).
-
(1990)
Cancer Commun.
, vol.2
, pp. 249-259
-
-
Thimmaiah, K.N.1
Horton, J.K.2
Qian, X.D.3
Beck, W.T.4
Houghton, J.A.5
Houghton, P.J.6
-
52
-
-
0026782599
-
Synthesis and chemical characterization of N-substituted phenoxazines directed toward reversing vinca alkaloid resistance in multidrug-resistant cancer cells
-
Thimmaiah, K. N., J. K. Horton, E. Seshadri, M. Israel, J. A. Houghton, F. C. Harwood, and P. J. Houghton. Synthesis and chemical characterization of N-substituted phenoxazines directed toward reversing vinca alkaloid resistance in multidrug-resistant cancer cells. J. Med. Chem. 35:3358-3364 (1992).
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3358-3364
-
-
Thimmaiah, K.N.1
Horton, J.K.2
Seshadri, E.3
Israel, M.4
Houghton, J.A.5
Harwood, F.C.6
Houghton, P.J.7
-
53
-
-
0028068790
-
Derivatives of a novel cyclopeptide. 2. Synthesis, activity against multidrug resistance in CHO and KB cells in vitro, and structure-activity relationships
-
Emmer, G., M. A. Grassberger, G. Schulz, D. Boesch, C. Gavenaux, and F. Loor. Derivatives of a novel cyclopeptide. 2. synthesis, activity against multidrug resistance in CHO and KB cells in vitro, and structure-activity relationships. J. Med. Chem. 37:1918-1928 (1994).
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1918-1928
-
-
Emmer, G.1
Grassberger, M.A.2
Schulz, G.3
Boesch, D.4
Gavenaux, C.5
Loor, F.6
-
54
-
-
0026635292
-
New triazine derivatives as potent modulators of multidrug resistance
-
Dhainaut, A., G. Regnier, G. Atassi, A. Pierre, S. Leonce, L. Kraus-Berthier and J. F. Prost. New triazine derivatives as potent modulators of multidrug resistance. J. Med. Chem. 35:2481-2496 (1992).
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2481-2496
-
-
Dhainaut, A.1
Regnier, G.2
Atassi, G.3
Pierre, A.4
Leonce, S.5
Kraus-Berthier, L.6
Prost, J.F.7
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