ARTICLE;
CALCEIN-AM ASSAY;
CANCER CELL LINE;
CHEMOSENSITIVITY;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
GENE EXPRESSION;
GENETIC TRANSFECTION;
HUMAN;
HUMAN CELL;
MULTIDRUG RESISTANCE;
ANTAGONISTS AND INHIBITORS;
CHEMISTRY;
DRUG DESIGN;
DRUG EFFECTS;
DRUG RESISTANCE;
GENE EXPRESSION REGULATION;
GENETICS;
METABOLISM;
PROTEIN CONFORMATION;
SYNTHESIS;
TUMOR CELL LINE;
CELL LINE, TUMOR;
CHEMISTRY TECHNIQUES, SYNTHETIC;
DRUG DESIGN;
DRUG RESISTANCE, MULTIPLE;
DRUG RESISTANCE, NEOPLASM;
GENE EXPRESSION REGULATION, NEOPLASTIC;
HUMANS;
P-GLYCOPROTEIN;
P-GLYCOPROTEINS;
PROTEIN CONFORMATION;
PYRANS;
RNA, MESSENGER;
New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells
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Design, synthesis and evaluation of novel triazole core based P-glycoprotein-mediated multidrug resistance reversal agents
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Chalcogenopyrylium dyes as inhibitors/modulators of P-glycoprotein in multidrug-resistant cells
G.A. Sawada, T.J. Raub, J. William Higgins, N.K. Brennan, T.M. Moore, G. Tombline, and M.R. Detty Chalcogenopyrylium dyes as inhibitors/modulators of P-glycoprotein in multidrug-resistant cells Bioorg. Med. Chem. 16 2008 9745 9756
Biochemical, cellular, and pharmacological aspects of the multidrug transporter
S.V. Ambudkar, S. Dey, C.A. Hrycyna, M. Ramachandra, I. Pastan, and M.M. Gottesman Biochemical, cellular, and pharmacological aspects of the multidrug transporter Annu. Rev. Pharmacol. Toxicol. 39 1999 361 398
Decreased accumulation of [14C]carboplatin in human cisplatin-resistant cells results from reduced energy-dependent uptake
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SAR studies on tetrahydroisoquinoline derivatives: The role of flexibility and bioisosterism to raise potency and selectivity toward P-glycoprotein
E. Capparelli, L. Zinzi, M. Cantore, M. Contino, M.G. Perrone, G. Luurtsema, F. Berardi, R. Perrone, and N.A. Colabufo SAR studies on tetrahydroisoquinoline derivatives: the role of flexibility and bioisosterism to raise potency and selectivity toward P-glycoprotein J. Med. Chem. 57 2014 9983 9994
Optimization of permethyl ningalin B analogs as P-glycoprotein inhibitors
Z. Wang, I.L. Wong, F.X. Li, C. Yang, Z. Liu, T. Jiang, T.F. Jiang, L.M. Chow, and S.B. Wan Optimization of permethyl ningalin B analogs as P-glycoprotein inhibitors Bioorg. Med. Chem. 23 2015 5566 5573
Overcoming of vincristine resistance in P388 leukemia in vivo and in vitro through enhanced cytotoxicity of vincristine and vinblastine by verapamil
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In vitro and in vivo chemosensitizing effect of cyclosporin A on an intrinsic multidrug-resistant rat colon tumour
W. Van de Vrie, E.E. Gheuens, N.M. Durante, E.A. De Bruijn, R.L. Marquet, A.T. Van Oosterom, and A.M. Eggermont In vitro and in vivo chemosensitizing effect of cyclosporin A on an intrinsic multidrug-resistant rat colon tumour J. Cancer Res. Clin. Oncol. 119 1993 609 614
Effects of quinidine and related compounds on cytotoxicity and cellular accumulation of vincristine and adriamycin in drug-resistant tumor cells
T. Tsuruo, H. Iida, Y. Kitatani, K. Yokota, S. Tsukagoshi, and Y. Sakurai Effects of quinidine and related compounds on cytotoxicity and cellular accumulation of vincristine and adriamycin in drug-resistant tumor cells Cancer Res. 44 1984 4303 4307
The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
V. Fischer, A. Rodriguez-Gascon, F. Heitz, R. Tynes, C. Hauck, D. Cohen, and A.E. Vickers The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite Drug Metab. Dispos. 26 1998 802 811
Phase II study of dexverapamil plus anthracycline in patients with metastatic breast cancer who have progressed on the same anthracycline regimen
E. Warner, D. Hedley, I. Andrulis, R. Myers, M. Trudeau, D. Warr, K.I. Pritchard, M. Blackstein, P.E. Goss, E. Franssen, K. Roche, S. Knight, S. Webster, R.A. Fraser, S. Oldfield, W. Hill, and R. Kates Phase II study of dexverapamil plus anthracycline in patients with metastatic breast cancer who have progressed on the same anthracycline regimen Clin. Cancer Res. 4 1998 1451 1457
Overcoming multidrug resistance in cancer: An update on the clinical strategy of inhibiting p-glycoprotein
H. Thomas, and H.M. Coley Overcoming multidrug resistance in cancer: an update on the clinical strategy of inhibiting p-glycoprotein Cancer control J. Moffitt Cancer Cent. 10 2003 159 165
Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma
L. Pusztai, P. Wagner, N. Ibrahim, E. Rivera, R. Theriault, D. Booser, F.W. Symmans, F. Wong, G. Blumenschein, D.R. Fleming, R. Rouzier, G. Boniface, and G.N. Hortobagyi Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma Cancer 104 2005 682 691
Brain accumulation of dasatinib is restricted by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and can be enhanced by elacridar treatment
J.S. Lagas, R.A. van Waterschoot, V.A. van Tilburg, M.J. Hillebrand, N. Lankheet, H. Rosing, J.H. Beijnen, and A.H. Schinkel Brain accumulation of dasatinib is restricted by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and can be enhanced by elacridar treatment Clin. Cancer Res. 15 2009 2344 2351
A phase I, randomized, open-label, parallel-cohort, dose-finding study of elacridar (GF120918) and oral topotecan in cancer patients
I.E. Kuppens, E.O. Witteveen, R.C. Jewell, S.A. Radema, E.M. Paul, S.G. Mangum, J.H. Beijnen, E.E. Voest, and J.H. Schellens A phase I, randomized, open-label, parallel-cohort, dose-finding study of elacridar (GF120918) and oral topotecan in cancer patients Clin. Cancer Res. 13 2007 3276 3285
Two isomeric benzodipyranone derivatives from Calophyllum inophyllum
N.U.-D. Khan, N. Parveen, M.P. Singh, R. Singh, B. Achari, P.P.G. Dastidar, and P.K. Dutta Two isomeric benzodipyranone derivatives from Calophyllum inophyllum Phytochemistry 42 1996 1181 1183
Benzodipyran derivatives with antiallergic activity
J.R. Bantick, H. Cairns, A. Chambers, R. Hazard, J. King, and T.B. Lee Benzodipyran derivatives with antiallergic activity J. Med. Chem. 19 1976 817 821
Functional impact of ABCB1 variants on interactions between P-glycoprotein and methadone
e59419
C.C. Hung, M.H. Chiou, Y.N. Teng, Y.W. Hsieh, C.L. Huang, and H.Y. Lane Functional impact of ABCB1 variants on interactions between P-glycoprotein and methadone PloS one 8 2013 e59419
YC-1, a novel potential anticancer agent, inhibit multidrug-resistant protein via cGMP-dependent pathway
C.C. Hung, and H.H. Liou YC-1, a novel potential anticancer agent, inhibit multidrug-resistant protein via cGMP-dependent pathway Investig. New Drugs 29 2011 1337 1346
Development of a novel class of tubulin inhibitor from desmosdumotin B with a hydroxylated bicyclic B-ring
K. Nakagawa-Goto, A. Oda, E. Hamel, E. Ohkoshi, K.H. Lee, and M. Goto Development of a novel class of tubulin inhibitor from desmosdumotin B with a hydroxylated bicyclic B-ring J. Med. Chem. 58 2015 2378 2389
Snapshots of ligand entry, malleable binding and induced helical movement in P-glycoprotein
P. Szewczyk, H. Tao, A.P. McGrath, M. Villaluz, S.D. Rees, S.C. Lee, R. Doshi, I.L. Urbatsch, Q. Zhang, and G. Chang Snapshots of ligand entry, malleable binding and induced helical movement in P-glycoprotein Acta Cryst. D. 71 2015 732 741