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Results: 1-13 |
Results: 13
INDOLEQUINONE ANTITUMOR AGENTS - RELATIONSHIP BETWEEN QUINONE STRUCTURE AND RATE OF METABOLISM BY RECOMBINANT HUMAN NQO1
Authors: BEALL HD HUDNOTT AR WINSKI S SIEGEL D SWANN E ROSS D MOODY CJ
Citation: Hd. Beall et al., INDOLEQUINONE ANTITUMOR AGENTS - RELATIONSHIP BETWEEN QUINONE STRUCTURE AND RATE OF METABOLISM BY RECOMBINANT HUMAN NQO1, Bioorganic & medicinal chemistry letters, 8(5), 1998, pp. 545-548
N-H INSERTION REACTIONS OF RHODIUM CARBENOIDS - A MODIFIED BISCHLER INDOLE SYNTHESIS
Authors: MOODY CJ SWANN E
Citation: Cj. Moody et E. Swann, N-H INSERTION REACTIONS OF RHODIUM CARBENOIDS - A MODIFIED BISCHLER INDOLE SYNTHESIS, Synlett, (2), 1998, pp. 135
RATIONAL DESIGN OF NOVEL BIOREDUCTIVELY-ACTIVATED PRODRUGS FOR THE TARGETED DELIVERY OF EFFECTOR MOLECULES TO TUMORS
Authors: EVERETT SA HUDNOTT AR MOODY CJ NAYLOR MA NOLAN J PATEL KB STRATFORD MRL SWANN E WARDMAN P
Citation: Sa. Everett et al., RATIONAL DESIGN OF NOVEL BIOREDUCTIVELY-ACTIVATED PRODRUGS FOR THE TARGETED DELIVERY OF EFFECTOR MOLECULES TO TUMORS, Annals of oncology, 9, 1998, pp. 111-111
INDOLEQUINONE ANTITUMOR AGENTS - CORRELATION BETWEEN QUINONE STRUCTURE, RATE OF METABOLISM BY RECOMBINANT HUMAN NAD(P)H-QUINONE OXIDOREDUCTASE, AND IN-VITRO CYTOTOXICITY
Authors: BEALL HD WINSKI S SWANN E HUDNOTT AR COTTERILL AS OSULLIVAN N GREEN SJ BIEN R SIEGEL D ROSS D MOODY CJ
Citation: Hd. Beall et al., INDOLEQUINONE ANTITUMOR AGENTS - CORRELATION BETWEEN QUINONE STRUCTURE, RATE OF METABOLISM BY RECOMBINANT HUMAN NAD(P)H-QUINONE OXIDOREDUCTASE, AND IN-VITRO CYTOTOXICITY, Journal of medicinal chemistry, 41(24), 1998, pp. 4755-4766
INDOLEQUINONE ANTITUMOR AGENTS - REDUCTIVE ACTIVATION AND ELIMINATIONFROM (5-METHOXY-1-METHYL-4,7-DIOXOINDOL-3-YL)METHYL DERIVATIVES AND HYPOXIA-SELECTIVE CYTOTOXICITY IN-VITRO
Authors: NAYLOR MA SWANN E EVERETT SA JAFFAR M NOLAN J ROBERTSON N LOCKYER SD PATEL KB DENNIS MF STRATFORD MRL WARDMAN P ADAMS GE MOODY CJ STRATFORD IJ
Citation: Ma. Naylor et al., INDOLEQUINONE ANTITUMOR AGENTS - REDUCTIVE ACTIVATION AND ELIMINATIONFROM (5-METHOXY-1-METHYL-4,7-DIOXOINDOL-3-YL)METHYL DERIVATIVES AND HYPOXIA-SELECTIVE CYTOTOXICITY IN-VITRO, Journal of medicinal chemistry, 41(15), 1998, pp. 2720-2731
A NEW APPROACH TO PEPTIDE-SYNTHESIS
Authors: MOODY CJ FERRIS L HAIGH D SWANN E
Citation: Cj. Moody et al., A NEW APPROACH TO PEPTIDE-SYNTHESIS, Chemical communications, (24), 1997, pp. 2391-2392
SYNTHESIS OF FUNCTIONALIZED FLUORESCENT DYES AND THEIR COUPLING TO AMINES AND AMINO-ACIDS
Authors: BRIGGS MSJ BRUCE I MILLER JN MOODY CJ SIMMONDS AC SWANN E
Citation: Msj. Briggs et al., SYNTHESIS OF FUNCTIONALIZED FLUORESCENT DYES AND THEIR COUPLING TO AMINES AND AMINO-ACIDS, Journal of the Chemical Society. Perkin transactions. I, (7), 1997, pp. 1051-1058
NOVEL BIOREDUCTIVE ANTICANCER AGENTS BASED ON INDOLEQUINONES
Authors: MOODY CJ SWANN E
Citation: Cj. Moody et E. Swann, NOVEL BIOREDUCTIVE ANTICANCER AGENTS BASED ON INDOLEQUINONES, Il Farmaco, 52(5), 1997, pp. 271-279
CHIRAL OXIMES IN ASYMMETRIC-SYNTHESIS - ADDITION OF ORGANOMETALLIC REAGENTS TO O-(1-PHENYLETHYL) ALDOXIMES
Authors: BROWN DS GALLAGHER PT LIGHTFOOT AP MOODY CJ SLAWIN AMZ SWANN E
Citation: Ds. Brown et al., CHIRAL OXIMES IN ASYMMETRIC-SYNTHESIS - ADDITION OF ORGANOMETALLIC REAGENTS TO O-(1-PHENYLETHYL) ALDOXIMES, Tetrahedron, 51(42), 1995, pp. 11473-11488
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF THIAZOLYLINDOLEQUINONES, ANALOGSOF THE NATURAL PRODUCT BE-10988
Authors: MOODY CJ SWANN E HOULBROOK S STEPHENS MA STRATFORD IJ
Citation: Cj. Moody et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF THIAZOLYLINDOLEQUINONES, ANALOGSOF THE NATURAL PRODUCT BE-10988, Journal of medicinal chemistry, 38(6), 1995, pp. 1039-1043
CYCLOPROPAMITOSENES, NOVEL BIOREDUCTIVE ANTICANCER AGENTS - SYNTHESISOF 7-METHOXYCYCLOPROPAMITOSENE AND RELATED INDOLEQUINONES
Authors: COTTERILL AS HARTOPP P JONES GB MOODY CJ NORTON CL OSULLIVAN N SWANN E
Citation: As. Cotterill et al., CYCLOPROPAMITOSENES, NOVEL BIOREDUCTIVE ANTICANCER AGENTS - SYNTHESISOF 7-METHOXYCYCLOPROPAMITOSENE AND RELATED INDOLEQUINONES, Tetrahedron, 50(25), 1994, pp. 7657-7674
CYCLOPROPAMITOSENES, NOVEL BIOREDUCTIVE ANTICANCER AGENTS - SYNTHESIS, ELECTROCHEMISTRY, AND BIOLOGICAL-ACTIVITY OF 7-SUBSTITUTED CYCLOPROPAMITOSENES AND RELATED INDOLEQUINONES
Authors: COTTERILL AS MOODY CJ MORTIMER RJ NORTON CL OSULLIVAN N STEPHENS MA STRADIOTTO NR SWANN E STRATFORD IJ
Citation: As. Cotterill et al., CYCLOPROPAMITOSENES, NOVEL BIOREDUCTIVE ANTICANCER AGENTS - SYNTHESIS, ELECTROCHEMISTRY, AND BIOLOGICAL-ACTIVITY OF 7-SUBSTITUTED CYCLOPROPAMITOSENES AND RELATED INDOLEQUINONES, Journal of medicinal chemistry, 37(22), 1994, pp. 3834-3843
SYNTHESIS OF THE NATURALLY-OCCURRING INDOLEQUINONE BE-10988, AN INHIBITOR OF TOPOISOMERASE-2
Authors: MOODY CJ SWANN E
Citation: Cj. Moody et E. Swann, SYNTHESIS OF THE NATURALLY-OCCURRING INDOLEQUINONE BE-10988, AN INHIBITOR OF TOPOISOMERASE-2, Journal of the Chemical Society. Perkin transactions. I, (21), 1993, pp. 2561-2565
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