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Kinetic Analysis of Calcein and Calcein−Acetoxymethylester Efflux Mediated by the Multidrug Resistance Protein and P-Glycoprotein

Biochemistry (Easton), 1998-02, Vol.37 (8), p.2243-2250

1998

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Preparation and cytotoxicity of cisplatin-containing liposomes

Brazilian journal of medical and biological research, 2007-08, Vol.40 (8), p.1149-1157

2007

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Kinetics of Anthracycline Efflux from Multidrug Resistance Protein-Expressing Cancer Cells Compared with P-Glycoprotein-Expressing Cancer Cells

Molecular pharmacology, 1998-01, Vol.53 (1), p.141-147

1998

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Anthrapyridones, a novel group of antitumour non‐cross resistant anthraquinone analogues. Synthesis and molecular basis of the cytotoxic activity towards K562/DOX cells

British journal of pharmacology, 2002-03, Vol.135 (6), p.1513-1523

2002

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Relation between the ability of some compounds to modulate the MRP1-mediated efflux of glutathione and to inhibit the MRPl-mediated efflux of daunorubicin

Biochemical pharmacology, 2004-12, Vol.68 (11), p.2159-2165

2004

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Analysis of drug transport kinetics in multidrug-resistant cells: implications for drug action

Current medicinal chemistry, 2001-01, Vol.8 (1), p.51-64

2001

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Relation among the resistance factor, kinetics of uptake, and kinetics of the P-glycoprotein-mediated efflux of doxorubicin, daunorubicin, 8-(S)-fluoroidarubicin, and idarubicin in multidrug-resistant K562 cells

Molecular pharmacology, 1996-03, Vol.49 (3), p.532

1996

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A Structural Model for the Open Conformation of the mdr1 P-glycoprotein Based on the MsbA Crystal Structure

The Journal of biological chemistry, 2003-08, Vol.278 (32), p.30115-30124

2003

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Structural Characterization of Ru−Bleomycin Complexes by Resonance Raman, Circular Dichroism, and NMR Spectroscopy

Inorganic chemistry, 2001-12, Vol.40 (27), p.6923-6929

2001

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Circular Dichroism Studies on Anthracycline Antitumor Compounds. Relationship between the Molecular Structure and the Spectroscopic Data

Journal of pharmaceutical sciences, 1998-08, Vol.87 (8), p.967-975

1998

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Mechanism of thioflavin T accumulation inside cells overexpressing P-glycoprotein or multidrug resistance-associated protein: Role of lipophilicity and positive charge

Biochemical and biophysical research communications, 2006-05, Vol.343 (2), p.623-629

2006

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Spectroscopic Studies on Iron Complexes of Different Anthracyclines in Aprotic Solvent Systems

Inorganic chemistry, 2001-10, Vol.40 (21), p.5324-5333

2001

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Comparison of the interaction of doxorubicin, daunorubicin, idarubicin and idarubicinol with large unilamellar vesicles: Circular dichroism study

Biochimica et biophysica acta, 1998-03, Vol.1370 (1), p.31-40

1998

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Perturbation of membrane microdomains in GLC4 multidrug‐resistant lung cancer cells − modification of ABCC1 (MRP1) localization and functionality

The FEBS journal, 2007-03, Vol.274 (6), p.1470-1480

2007

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Kinetics of glutathione and daunorubicin efflux from multidrug resistance protein overexpressing small-cell lung cancer cells

European journal of pharmacology, 2001-06, Vol.421 (1), p.1-9

2001

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DNA-containing liposomes as a model for the study of cell membrane permeation by anthracycline derivatives

Biochemistry (Easton), 1991-05, Vol.30 (20), p.5038-5043

1991

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Exploratory Chemistry toward the Identification of a New Class of Multidrug Resistance Reverters Inspired by Pervilleine and Verapamil Models

Journal of medicinal chemistry, 2005-11, Vol.48 (23), p.7426-7436

2005

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Ability of carbazole salts, inhibitors of Alzheimer β-amyloid fibril formation, to cross cellular membranes

European journal of pharmacology, 2007-03, Vol.559 (2), p.124-131

2007

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Accumulation of Eu3+ chelates in cells expressing or not P-glycoprotein: implications for blood-brain barrier crossing

Journal of inorganic biochemistry, 2010-01, Vol.104 (1), p.47-54

2010

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Isomeric N,N-Bis(cyclohexanol)amine Aryl Esters: The Discovery of a New Class of Highly Potent P-Glycoprotein (Pgp)-dependent Multidrug Resistance (MDR) Inhibitors

Journal of medicinal chemistry, 2007-02, Vol.50 (4), p.599-602

2007

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Iron(III)-adriamycin and iron(III)-daunorubicin complexes: physicochemical characteristics, interaction with DNA, and antitumor activity

Biochemistry (Easton), 1985-01, Vol.24 (2), p.284-289

1985

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Impact of intracellular chloride concentration on cisplatin accumulation in sensitive and resistant GLC4 cells

Journal of biological inorganic chemistry, 2009, Vol.14 (1), p.123-132

2009

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The MRP1-mediated effluxes of arsenic and antimony do not require arsenic-glutathione and antimony-glutathione complex formation

Journal of bioenergetics and biomembranes, 2002-04, Vol.34 (2), p.135-145

2002

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Kinetic analysis of fluorescein and dihydrofluorescein effluxes in tumour cells expressing the multidrug resistance protein, MRP1

Biochemical pharmacology, 2003-03, Vol.65 (6), p.969-977

2003

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Impaired hydrolysis of cisplatin derivatives to aquated species prevents energy-dependent uptake in GLC4 cells resistant to cisplatin

Journal of biological inorganic chemistry, 2003-07, Vol.8 (6), p.626-634

2003

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Kinetic Analysis of Calcein and Calcein−Acetoxymethylester Efflux Mediated by the Multidrug Resistance Protein and P-Glycoprotein

Preparation and cytotoxicity of cisplatin-containing liposomes

Kinetics of Anthracycline Efflux from Multidrug Resistance Protein-Expressing Cancer Cells Compared with P-Glycoprotein-Expressing Cancer Cells

Anthrapyridones, a novel group of antitumour non‐cross resistant anthraquinone analogues. Synthesis and molecular basis of the cytotoxic activity towards K562/DOX cells

Relation between the ability of some compounds to modulate the MRP1-mediated efflux of glutathione and to inhibit the MRPl-mediated efflux of daunorubicin

Analysis of drug transport kinetics in multidrug-resistant cells: implications for drug action

Relation among the resistance factor, kinetics of uptake, and kinetics of the P-glycoprotein-mediated efflux of doxorubicin, daunorubicin, 8-(S)-fluoroidarubicin, and idarubicin in multidrug-resistant K562 cells

A Structural Model for the Open Conformation of the mdr1 P-glycoprotein Based on the MsbA Crystal Structure

Structural Characterization of Ru−Bleomycin Complexes by Resonance Raman, Circular Dichroism, and NMR Spectroscopy

Circular Dichroism Studies on Anthracycline Antitumor Compounds. Relationship between the Molecular Structure and the Spectroscopic Data

Mechanism of thioflavin T accumulation inside cells overexpressing P-glycoprotein or multidrug resistance-associated protein: Role of lipophilicity and positive charge

Spectroscopic Studies on Iron Complexes of Different Anthracyclines in Aprotic Solvent Systems

Comparison of the interaction of doxorubicin, daunorubicin, idarubicin and idarubicinol with large unilamellar vesicles: Circular dichroism study

Perturbation of membrane microdomains in GLC4 multidrug‐resistant lung cancer cells − modification of ABCC1 (MRP1) localization and functionality

Kinetics of glutathione and daunorubicin efflux from multidrug resistance protein overexpressing small-cell lung cancer cells

DNA-containing liposomes as a model for the study of cell membrane permeation by anthracycline derivatives

Exploratory Chemistry toward the Identification of a New Class of Multidrug Resistance Reverters Inspired by Pervilleine and Verapamil Models

Ability of carbazole salts, inhibitors of Alzheimer β-amyloid fibril formation, to cross cellular membranes

Accumulation of Eu3+ chelates in cells expressing or not P-glycoprotein: implications for blood-brain barrier crossing

Isomeric N,N-Bis(cyclohexanol)amine Aryl Esters: The Discovery of a New Class of Highly Potent P-Glycoprotein (Pgp)-dependent Multidrug Resistance (MDR) Inhibitors

Iron(III)-adriamycin and iron(III)-daunorubicin complexes: physicochemical characteristics, interaction with DNA, and antitumor activity

Impact of intracellular chloride concentration on cisplatin accumulation in sensitive and resistant GLC4 cells

The MRP1-mediated effluxes of arsenic and antimony do not require arsenic-glutathione and antimony-glutathione complex formation

Kinetic analysis of fluorescein and dihydrofluorescein effluxes in tumour cells expressing the multidrug resistance protein, MRP1

Impaired hydrolysis of cisplatin derivatives to aquated species prevents energy-dependent uptake in GLC4 cells resistant to cisplatin

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