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Results: 1-15 |
Results: 15
THE ORTHO-QUINONE METABOLITE OF THE ANTICANCER DRUG ETOPOSIDE (VP-16)IS A POTENT INHIBITOR OF THE TOPOISOMERASE-II DNA CLEAVABLE COMPLEX
Authors: GANTCHEV TG HUNTING DJ
Citation: Tg. Gantchev et Dj. Hunting, THE ORTHO-QUINONE METABOLITE OF THE ANTICANCER DRUG ETOPOSIDE (VP-16)IS A POTENT INHIBITOR OF THE TOPOISOMERASE-II DNA CLEAVABLE COMPLEX, Molecular pharmacology, 53(3), 1998, pp. 422-428
ENHANCEMENT OF ETOPOSIDE (VP-16) CYTOTOXICITY BY ENZYMATIC AND PHOTODYNAMICALLY INDUCED OXIDATIVE STRESS
Authors: GANTCHEV TG HUNTING DJ
Citation: Tg. Gantchev et Dj. Hunting, ENHANCEMENT OF ETOPOSIDE (VP-16) CYTOTOXICITY BY ENZYMATIC AND PHOTODYNAMICALLY INDUCED OXIDATIVE STRESS, Anti-cancer drugs, 8(2), 1997, pp. 164-173
INHIBITION OF THE TOPOISOMERASE-II DNA CLEAVABLE COMPLEX BY THE ORTHO-QUINONE DERIVATIVE OF THE ANTITUMOR DRUG ETOPOSIDE (VP-16)
Authors: GANTCHEV TG HUNTING DJ
Citation: Tg. Gantchev et Dj. Hunting, INHIBITION OF THE TOPOISOMERASE-II DNA CLEAVABLE COMPLEX BY THE ORTHO-QUINONE DERIVATIVE OF THE ANTITUMOR DRUG ETOPOSIDE (VP-16), Biochemical and biophysical research communications, 237(1), 1997, pp. 24-27
COMBINATION TOXICITY OF ETOPOSIDE (VP-16) AND PHOTOSENSITIZATION WITHA WATER-SOLUBLE ALUMINUM PHTHALOCYANINE IN K562 HUMAN LEUKEMIC-CELLS
Authors: GANTCHEV TG BRASSEUR N VANLIER JE
Citation: Tg. Gantchev et al., COMBINATION TOXICITY OF ETOPOSIDE (VP-16) AND PHOTOSENSITIZATION WITHA WATER-SOLUBLE ALUMINUM PHTHALOCYANINE IN K562 HUMAN LEUKEMIC-CELLS, British Journal of Cancer, 74(10), 1996, pp. 1570-1577
HEMATOPORPHYRIN-SENSITIZED DEGRADATION OF DEOXYRIBOSE AND DNA IN HIGH-INTENSITY NEAR-UV PICOSECOND PULSED-LASER PHOTOLYSIS
Authors: GANTCHEV TG GRABNER G KESKINOVA E ANGELOV D VANLIER JE
Citation: Tg. Gantchev et al., HEMATOPORPHYRIN-SENSITIZED DEGRADATION OF DEOXYRIBOSE AND DNA IN HIGH-INTENSITY NEAR-UV PICOSECOND PULSED-LASER PHOTOLYSIS, Radiation physics and chemistry, 45(1), 1995, pp. 111-119
THYMIDINE FREE-RADICALS GENERATED DURING METALLO-PHTHALOCYANINE PHOTOSENSITIZATION - A COMPARISON WITH GAMMA-RADIATION
Authors: GANTCHEV TG
Citation: Tg. Gantchev, THYMIDINE FREE-RADICALS GENERATED DURING METALLO-PHTHALOCYANINE PHOTOSENSITIZATION - A COMPARISON WITH GAMMA-RADIATION, International journal of radiation biology, 68(1), 1995, pp. 29-36
CATALASE INACTIVATION FOLLOWING PHOTOSENSITIZATION WITH TETRASULFONATED METALLOPHTHALOCYANINES
Authors: GANTCHEV TG VANLIER JE
Citation: Tg. Gantchev et Je. Vanlier, CATALASE INACTIVATION FOLLOWING PHOTOSENSITIZATION WITH TETRASULFONATED METALLOPHTHALOCYANINES, Photochemistry and photobiology, 62(1), 1995, pp. 123-134
DNA STRAND SCISSION AND BASE RELEASE PHOTOSENSITIZED BY METALLO-PHTHALOCYANINES
Authors: GANTCHEV TG GOWANS BJ HUNTING DJ WAGNER JR VANLIER JE
Citation: Tg. Gantchev et al., DNA STRAND SCISSION AND BASE RELEASE PHOTOSENSITIZED BY METALLO-PHTHALOCYANINES, International journal of radiation biology, 66(6), 1994, pp. 705-716
PHOTOCYTOTOXICITY AND INTRACELLULAR GENERATION OF FREE-RADICALS BY TETRASULFONATED AL-PHTHALOCYANINES AND ZN-PHTHALOCYANINES
Authors: GANTCHEV TG URUMOV IJ HUNTING DJ VANLIER JE
Citation: Tg. Gantchev et al., PHOTOCYTOTOXICITY AND INTRACELLULAR GENERATION OF FREE-RADICALS BY TETRASULFONATED AL-PHTHALOCYANINES AND ZN-PHTHALOCYANINES, International journal of radiation biology, 65(3), 1994, pp. 289-298
ON THE RELATIONSHIP BETWEEN RATE OF UPTAKE OF PHOTOFRIN AND CELLULAR-RESPONSES TO PHOTODYNAMIC TREATMENT IN-VITRO
Authors: GANTCHEV TG URUMOV IJ VANLIER JE
Citation: Tg. Gantchev et al., ON THE RELATIONSHIP BETWEEN RATE OF UPTAKE OF PHOTOFRIN AND CELLULAR-RESPONSES TO PHOTODYNAMIC TREATMENT IN-VITRO, Cancer biochemistry biophysics, 14(1), 1994, pp. 23-34
QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS COMPARATIVE MOLECULAR-FIELD ANALYSIS (QSAR COMFA) FOR RECEPTOR-BINDING PROPERTIES OF HALOGENATED ESTRADIOL DERIVATIVES/
Authors: GANTCHEV TG ALI H VANLIER JE
Citation: Tg. Gantchev et al., QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS COMPARATIVE MOLECULAR-FIELD ANALYSIS (QSAR COMFA) FOR RECEPTOR-BINDING PROPERTIES OF HALOGENATED ESTRADIOL DERIVATIVES/, Journal of medicinal chemistry, 37(24), 1994, pp. 4164-4176
ASCORBATE IS THE PRIMARY REDUCTANT OF THE PHENOXYL RADICAL OF ETOPOSIDE IN THE PRESENCE OF THIOLS BOTH IN CELL HOMOGENATES AND IN MODEL SYSTEMS
Authors: KAGAN VE YALOWICH JC DAY BW GOLDMAN R GANTCHEV TG STOYANOVSKY DA
Citation: Ve. Kagan et al., ASCORBATE IS THE PRIMARY REDUCTANT OF THE PHENOXYL RADICAL OF ETOPOSIDE IN THE PRESENCE OF THIOLS BOTH IN CELL HOMOGENATES AND IN MODEL SYSTEMS, Biochemistry, 33(32), 1994, pp. 9651-9660
2 FACES OF THE PHENOLIC ANTITUMOR DRUG ETOPOSIDE (VP-16) - FREE-RADICAL ENHANCEMENT OF CYTOTOXICITY AND PROTECTION AGAINST FREE RADICAL-INDUCED DNA-DAMAGE
Authors: YALOWICH JC CLAYCAMP HG STOYANOVSKY DA ALLAN W GANTCHEV TG DAY BW KAGAN VE
Citation: Jc. Yalowich et al., 2 FACES OF THE PHENOLIC ANTITUMOR DRUG ETOPOSIDE (VP-16) - FREE-RADICAL ENHANCEMENT OF CYTOTOXICITY AND PROTECTION AGAINST FREE RADICAL-INDUCED DNA-DAMAGE, Free radical biology & medicine, 15(5), 1993, pp. 493-493
2-FLUORINATED AND 4-FLUORINATED 16-ALPHA-[I-125]IODOESTRADIOL DERIVATIVES - SYNTHESIS AND EFFECT ON ESTROGEN-RECEPTOR BINDING AND RECEPTOR-MEDIATED TARGET TISSUE UPTAKE
Authors: ALI H ROUSSEAU J GANTCHEV TG VANLIER JE
Citation: H. Ali et al., 2-FLUORINATED AND 4-FLUORINATED 16-ALPHA-[I-125]IODOESTRADIOL DERIVATIVES - SYNTHESIS AND EFFECT ON ESTROGEN-RECEPTOR BINDING AND RECEPTOR-MEDIATED TARGET TISSUE UPTAKE, Journal of medicinal chemistry, 36(26), 1993, pp. 4255-4263
INTERACTIONS OF ROALUMINIUM-TETRAMETHYL-TETRAPYRIDINO-PORPHYRAZINE WITH DNA
Authors: GANTCHEV TG ALI H VANLIER JE
Citation: Tg. Gantchev et al., INTERACTIONS OF ROALUMINIUM-TETRAMETHYL-TETRAPYRIDINO-PORPHYRAZINE WITH DNA, European journal of biochemistry, 217(1), 1993, pp. 371-376
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