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Antimicrobial activities of clofazimine and B669 are mediated by lysophospholipids

Antimicrobial Agents and Chemotherapy, 1992-12, Vol.36 (12), p.2729-2735

1992

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In vitro Investigation of the Antimicrobial Activities of Novel Tetramethylpiperidine- Substituted Phenazines against Mycobacterium tuberculosis

Chemotherapy (Basel), 2000-01, Vol.46 (1), p.43-48

2000

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An in vitro investigation of the anti-inflammatory properties of potassium humate

Inflammation, 2004-06, Vol.28 (3), p.169-174

2004

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Clofazimine and B4121 sensitize an intrinsically resistant human colon cancer cell line to P-glycoprotein substrates

Oncology reports, 2000-01, Vol.7 (1), p.193

2000

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Vitamin C and cellular immune functions: protection against hypochlorous acid-mediated inactivation of glyceraldehyde-3-phosphate dehydrogenase and ATP generation in human leukocytes as a possible mechanism of ascorbate-mediated immunostimulation

Annals of the New York Academy of Sciences, 1990, Vol.587 (1), p.34-48

1990

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The riminophenazine agents clofazimine and B669 reverse acquired multidrug resistance in a human lung cancer cell line

Cancer letters, 1994-09, Vol.85 (1), p.59-63

1994

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α-Tocopherol antagonizes the multidrug-resistance-reversal activity of cyclosporin A, verapamil, GF120918, clofazimine and B669

Cancer letters, 1998-05, Vol.127 (1), p.107-112

1998

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B4112, a Novel Tetramethylpiperidine-Substituted Phenazine That Inhibits the Proliferation of Multidrug-Resistant Cancer Cell Lines

Annals of the New York Academy of Sciences, 1999-01, Vol.886 (1), p.280-282

1999

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In vitro investigation of the intraphagocytic bioactivities of ciprofloxacin and the new fluoroquinolone agents, clinafloxacin (CI-960) and PD 131628

Chemotherapy (Basel), 1993-11, Vol.39 (6), p.424

1993

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An in vitro investigation of the bioactivities of ciprofloxacin and the new fluoroquinolone agents clinafloxacin (CI-960) and PD 131628 against Mycobacterium tuberculosis in human macrophages

Chemotherapy (Basel), 1995-07, Vol.41 (4), p.234

1995

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Tetramethylpiperidine-substitution increases the antitumor activity of the riminophenazines for an acquired multidrug-resistant cell line

Anti-cancer drug design, 2000-08, Vol.15 (4), p.303

2000

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Clindamycin, erythromycin, and roxithromycin inhibit the proinflammatory interactions of Pseudomonas aeruginosa pigments with human neutrophils in vitro

Antimicrobial Agents and Chemotherapy, 1992-06, Vol.36 (6), p.1236-1240

1992

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The chemosensitizing potential of GF120918 is independent of the magnitude of P-glycoprotein-mediated resistance to conventional chemotherapeutic agents in a small cell lung cancer line

Oncology reports, 1999-01, Vol.6 (1), p.217

1999

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Tetramethylpiperidine-substituted phenazines inhibit the proliferation of intrinsically multidrug resistant carcinoma cell lines

Investigational new drugs, 2001-01, Vol.19 (3), p.211-217

2001

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Auranofin inactivates phosphofructokinase in human neutrophils, leading to depletion of intracellular ATP and inhibition of superoxide generation and locomotion

Molecular pharmacology, 1991-09, Vol.40 (3), p.427-434

1991

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Interactions of the oxygen-dependent antimicrobial system of the human neutrophil with difloxacin, ciprofloxacin, pefloxacin and fleroxacin in the intraphagocytic eradication of Staphylococcus aureus

Journal of medical microbiology, 1990-05, Vol.32 (1), p.15-17

1990

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An in vitro investigation of the intracellular bioactivity of amoxicillin, clindamycin, and erythromycin for Staphylococcus aureus

The Journal of infectious diseases, 1986-03, Vol.153 (3), p.593

1986

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Synthesis, characterization and antitumor properties of titanocene derivatives with thiophene containing ligands

Journal of organometallic chemistry, 2005-01, Vol.690 (1), p.117-125

2005

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An in-vitro evaluation of the cellular uptake and intraphagocytic bioactivity of clarithromycin (A-56268, TE-031), a new macrolide antimicrobial agent

Journal of antimicrobial chemotherapy, 1988-12, Vol.22 (6), p.923-933

1988

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Novel tetramethylpiperidine-substituted phenazines are potent inhibitors of P-glycoprotein activity in a multidrug resistant cancer cell line

Anti-cancer drugs, 1997-08, Vol.8 (7), p.708-713

1997

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An in vitro investigation of the intraphagocytic bioactivity of difloxacin, ciprofloxacin, pefloxacin and fleroxacin

Chemotherapy (Basel), 1989, Vol.35 (4), p.273

1989

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a-tocopherol antagonizes the multidrug-resistance-reversal activity of cyclosporin A, verapamil, GF120918, clofazimine and B669

Cancer letters, 1998, Vol.127 (1-2), p.107-112

1998

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Investigation of the Immunostimulatory Properties of Oxihumate

Zeitschrift für Naturforschung C. A journal of biosciences, 2003-03, Vol.58 (3), p.263-267

2003

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An in-vitro comparison of the intraphagocytic bioactivity of erythromycin and roxithromycin

Journal of antimicrobial chemotherapy, 1987-01, Vol.20 (suppl-B), p.57-68

1987

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Comparison of the composition and opsonic activities of imported and South African-manufactured intravenous and intramuscular immunoglobulin preparations

South African medical journal, 1994-11, Vol.84 (11), p.743-746

1994

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Antimicrobial activities of clofazimine and B669 are mediated by lysophospholipids

In vitro Investigation of the Antimicrobial Activities of Novel Tetramethylpiperidine- Substituted Phenazines against Mycobacterium tuberculosis

An in vitro investigation of the anti-inflammatory properties of potassium humate

Clofazimine and B4121 sensitize an intrinsically resistant human colon cancer cell line to P-glycoprotein substrates

Vitamin C and cellular immune functions: protection against hypochlorous acid-mediated inactivation of glyceraldehyde-3-phosphate dehydrogenase and ATP generation in human leukocytes as a possible mechanism of ascorbate-mediated immunostimulation

The riminophenazine agents clofazimine and B669 reverse acquired multidrug resistance in a human lung cancer cell line

α-Tocopherol antagonizes the multidrug-resistance-reversal activity of cyclosporin A, verapamil, GF120918, clofazimine and B669

B4112, a Novel Tetramethylpiperidine-Substituted Phenazine That Inhibits the Proliferation of Multidrug-Resistant Cancer Cell Lines

In vitro investigation of the intraphagocytic bioactivities of ciprofloxacin and the new fluoroquinolone agents, clinafloxacin (CI-960) and PD 131628

An in vitro investigation of the bioactivities of ciprofloxacin and the new fluoroquinolone agents clinafloxacin (CI-960) and PD 131628 against Mycobacterium tuberculosis in human macrophages

Tetramethylpiperidine-substitution increases the antitumor activity of the riminophenazines for an acquired multidrug-resistant cell line

Clindamycin, erythromycin, and roxithromycin inhibit the proinflammatory interactions of Pseudomonas aeruginosa pigments with human neutrophils in vitro

The chemosensitizing potential of GF120918 is independent of the magnitude of P-glycoprotein-mediated resistance to conventional chemotherapeutic agents in a small cell lung cancer line

Tetramethylpiperidine-substituted phenazines inhibit the proliferation of intrinsically multidrug resistant carcinoma cell lines

Auranofin inactivates phosphofructokinase in human neutrophils, leading to depletion of intracellular ATP and inhibition of superoxide generation and locomotion

Interactions of the oxygen-dependent antimicrobial system of the human neutrophil with difloxacin, ciprofloxacin, pefloxacin and fleroxacin in the intraphagocytic eradication of Staphylococcus aureus

An in vitro investigation of the intracellular bioactivity of amoxicillin, clindamycin, and erythromycin for Staphylococcus aureus

Synthesis, characterization and antitumor properties of titanocene derivatives with thiophene containing ligands

An in-vitro evaluation of the cellular uptake and intraphagocytic bioactivity of clarithromycin (A-56268, TE-031), a new macrolide antimicrobial agent

Novel tetramethylpiperidine-substituted phenazines are potent inhibitors of P-glycoprotein activity in a multidrug resistant cancer cell line

An in vitro investigation of the intraphagocytic bioactivity of difloxacin, ciprofloxacin, pefloxacin and fleroxacin

a-tocopherol antagonizes the multidrug-resistance-reversal activity of cyclosporin A, verapamil, GF120918, clofazimine and B669

Investigation of the Immunostimulatory Properties of Oxihumate

An in-vitro comparison of the intraphagocytic bioactivity of erythromycin and roxithromycin

Comparison of the composition and opsonic activities of imported and South African-manufactured intravenous and intramuscular immunoglobulin preparations

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