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Results: 1-13 |
Results: 13
SYNTHESIS OF NITROGEN AND SULFUR ANALOGS OF THE SECO-CI ALKYLATING AGENT
Authors: TERCEL M DENNY WA
Citation: M. Tercel et Wa. Denny, SYNTHESIS OF NITROGEN AND SULFUR ANALOGS OF THE SECO-CI ALKYLATING AGENT, Journal of the Chemical Society. Perkin transactions. I, (3), 1998, pp. 509-519
REDUCTION OF NITROARYLMETHYL QUATERNARY AMMONIUM PRODRUGS OF MECHLORETHAMINE BY RADIATION
Authors: WILSON WR FERRY DM TERCEL M ANDERSON RF DENNY WA
Citation: Wr. Wilson et al., REDUCTION OF NITROARYLMETHYL QUATERNARY AMMONIUM PRODRUGS OF MECHLORETHAMINE BY RADIATION, Radiation research, 149(3), 1998, pp. 237-245
PULSE-RADIOLYSIS STUDIES ON THE FRAGMENTATION OF ARYLMETHYL QUATERNARY NITROGEN MUSTARDS BY ONE-ELECTRON REDUCTION IN AQUEOUS-SOLUTION
Authors: ANDERSON RF DENNY WA LI WJ PACKER JE TERCEL M WILSON WR
Citation: Rf. Anderson et al., PULSE-RADIOLYSIS STUDIES ON THE FRAGMENTATION OF ARYLMETHYL QUATERNARY NITROGEN MUSTARDS BY ONE-ELECTRON REDUCTION IN AQUEOUS-SOLUTION, The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 101(50), 1997, pp. 9704-9709
SYNTHESIS, DNA-BINDING AND CYTOTOXICITY OF LKYL]CARBONYL-3-(CHLOROMETHYL)-6-HYDROXYINDOLINES, A NEW CLASS OF DNA-TARGETED ALKYLATING-AGENTS
Authors: FAN JY TERCEL M DENNY WA
Citation: Jy. Fan et al., SYNTHESIS, DNA-BINDING AND CYTOTOXICITY OF LKYL]CARBONYL-3-(CHLOROMETHYL)-6-HYDROXYINDOLINES, A NEW CLASS OF DNA-TARGETED ALKYLATING-AGENTS, Anti-cancer drug design, 12(4), 1997, pp. 277-293
NITROGEN AND SULFUR ANALOGS OF THE SECO-CO ALKYLATING AGENT - SYNTHESIS AND CYTOTOXICITY
Authors: TERCEL M DENNY WA WILSON WR
Citation: M. Tercel et al., NITROGEN AND SULFUR ANALOGS OF THE SECO-CO ALKYLATING AGENT - SYNTHESIS AND CYTOTOXICITY, Bioorganic & medicinal chemistry letters, 6(22), 1996, pp. 2735-2740
A NOVEL NITROSUBSTITUTED SECO-CI - APPLICATION AS A REDUCTIVELY ACTIVATED ADEPT PRODRUG
Authors: TERCEL M DENNY WA WILSON WR
Citation: M. Tercel et al., A NOVEL NITROSUBSTITUTED SECO-CI - APPLICATION AS A REDUCTIVELY ACTIVATED ADEPT PRODRUG, Bioorganic & medicinal chemistry letters, 6(22), 1996, pp. 2741-2744
HYPOXIA-SELECTIVE ANTITUMOR AGENTS .12. NITROBENZYL QUATERNARY-SALTS AS BIOREDUCTIVE PRODRUGS OF THE ALKYLATING AGENT MECHLORETHAMINE
Authors: TERCEL M WILSON WR ANDERSON RF DENNY WA
Citation: M. Tercel et al., HYPOXIA-SELECTIVE ANTITUMOR AGENTS .12. NITROBENZYL QUATERNARY-SALTS AS BIOREDUCTIVE PRODRUGS OF THE ALKYLATING AGENT MECHLORETHAMINE, Journal of medicinal chemistry, 39(5), 1996, pp. 1084-1094
HYPOXIA-SELECTIVE ANTITUMOR AGENTS .11. CHLORAMBUCIL N-OXIDE - A REAPPRAISAL OF ITS SYNTHESIS, STABILITY, AND SELECTIVE TOXICITY FOR HYPOXIC CELLS
Authors: TERCEL M WILSON WR DENNY WA
Citation: M. Tercel et al., HYPOXIA-SELECTIVE ANTITUMOR AGENTS .11. CHLORAMBUCIL N-OXIDE - A REAPPRAISAL OF ITS SYNTHESIS, STABILITY, AND SELECTIVE TOXICITY FOR HYPOXIC CELLS, Journal of medicinal chemistry, 38(7), 1995, pp. 1247-1252
SYNTHESIS AND PROPERTIES OF A VERTICALLY STACKED PORPHYRIN-QUINONE(1)QUINONE(2) CYCLOPHANE
Authors: STAAB HA TERCEL M FISCHER R KRIEGER C
Citation: Ha. Staab et al., SYNTHESIS AND PROPERTIES OF A VERTICALLY STACKED PORPHYRIN-QUINONE(1)QUINONE(2) CYCLOPHANE, Angewandte Chemie, International Edition in English, 33(14), 1994, pp. 1463-1466
NITROBENZYL MUSTARD QUATERNARY-SALTS - A NEW CLASS OF HYPOXIA-SELECTIVE CYTOTOXINS CAPABLE OF RELEASING DIFFUSIBLE CYTOTOXINS ON BIOREDUCTION
Authors: DENNY WA WILSON WR TERCEL M VANZIJL P PULLEN SM
Citation: Wa. Denny et al., NITROBENZYL MUSTARD QUATERNARY-SALTS - A NEW CLASS OF HYPOXIA-SELECTIVE CYTOTOXINS CAPABLE OF RELEASING DIFFUSIBLE CYTOTOXINS ON BIOREDUCTION, International journal of radiation oncology, biology, physics, 29(2), 1994, pp. 317-321
TYROSINE KINASE INHIBITORS .1. STRUCTURE-ACTIVITY-RELATIONSHIPS FOR INHIBITION OF EPIDERMAL GROWTH-FACTOR RECEPTOR TYROSINE KINASE-ACTIVITYBY 2,3-DIHYDRO-2-THIOXO-1H-INDOLE-3-ALKANOIC ACIDS AND 2,2'-DITHIOBIS(1H-INDOLE-3-ALKANOIC ACIDS)
Authors: THOMPSON AM REWCASTLE GW TERCEL M DOBRUSIN EM FRY DW KRAKER AJ DENNY WA
Citation: Am. Thompson et al., TYROSINE KINASE INHIBITORS .1. STRUCTURE-ACTIVITY-RELATIONSHIPS FOR INHIBITION OF EPIDERMAL GROWTH-FACTOR RECEPTOR TYROSINE KINASE-ACTIVITYBY 2,3-DIHYDRO-2-THIOXO-1H-INDOLE-3-ALKANOIC ACIDS AND 2,2'-DITHIOBIS(1H-INDOLE-3-ALKANOIC ACIDS), Journal of medicinal chemistry, 36(17), 1993, pp. 2459-2469
NITROBENZYL MUSTARD QUATERNARY-SALTS - A NEW CLASS OF HYPOXIA-SELECTIVE CYTOTOXINS SHOWING VERY HIGH IN-VITRO SELECTIVITY
Authors: TERCEL M WILSON WR DENNY WA
Citation: M. Tercel et al., NITROBENZYL MUSTARD QUATERNARY-SALTS - A NEW CLASS OF HYPOXIA-SELECTIVE CYTOTOXINS SHOWING VERY HIGH IN-VITRO SELECTIVITY, Journal of medicinal chemistry, 36(17), 1993, pp. 2578-2579
STACKED PORPHYRIN QUINONE TRIADS AS MODELS FOR THE PRIMARY CHARGE-SEPARATION IN PHOTOSYNTHESIS
Authors: POLLINGER F HEITELE H MICHELBEYERLE ME TERCEL M STAAB HA
Citation: F. Pollinger et al., STACKED PORPHYRIN QUINONE TRIADS AS MODELS FOR THE PRIMARY CHARGE-SEPARATION IN PHOTOSYNTHESIS, Chemical physics letters, 209(3), 1993, pp. 251-257
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