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Results: 1-25 | 26-26
Results: 1-25/26
SYNTHESIS OF 3-SUBSTITUTED BENZAMIDES AND 5-SUBSTITUTED ISOQUINOLIN-1(2H)-ONES AND PRELIMINARY EVALUATION AS INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP)
Authors: WATSON CY WHISH WJD THREADGILL MD
Citation: Cy. Watson et al., SYNTHESIS OF 3-SUBSTITUTED BENZAMIDES AND 5-SUBSTITUTED ISOQUINOLIN-1(2H)-ONES AND PRELIMINARY EVALUATION AS INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP), Bioorganic & medicinal chemistry, 6(6), 1998, pp. 721-734
8-(OMEGA-AMINOALKYL)THEOPHYLLINES AND THEIR USE IN PREPARING FLUORESCENTLY LABELED DERIVATIVES FOR APPLICATIONS IN IMMUNOASSAY
Authors: YAHIOGLU F POUTON CW THREADGILL MD
Citation: F. Yahioglu et al., 8-(OMEGA-AMINOALKYL)THEOPHYLLINES AND THEIR USE IN PREPARING FLUORESCENTLY LABELED DERIVATIVES FOR APPLICATIONS IN IMMUNOASSAY, Bioconjugate chemistry, 8(4), 1997, pp. 611-616
LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .5. SYNTHESIS OF [O-18]-5-METHYLISOQUINOLINONE AND 1-(FURAN-2-YL-[O-18]-METHOXY)-5-METHYLISOQUINOLINE (VOL 38, PG 935, 1996)
Authors: BERRY JM THREADGILL MD
Citation: Jm. Berry et Md. Threadgill, LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .5. SYNTHESIS OF [O-18]-5-METHYLISOQUINOLINONE AND 1-(FURAN-2-YL-[O-18]-METHOXY)-5-METHYLISOQUINOLINE (VOL 38, PG 935, 1996), Journal of labelled compounds & radiopharmaceuticals, 39(5), 1997, pp. 453-453
5-NITROFURAN-2-YLMETHYL GROUP AS A POTENTIAL BIOREDUCTIVELY ACTIVATEDPRO-DRUG SYSTEM
Authors: BERRY JM WATSON CY WHISH WJD THREADGILL MD
Citation: Jm. Berry et al., 5-NITROFURAN-2-YLMETHYL GROUP AS A POTENTIAL BIOREDUCTIVELY ACTIVATEDPRO-DRUG SYSTEM, Journal of the Chemical Society. Perkin transactions. I, (8), 1997, pp. 1147-1156
S-2-AMINO-5-(2-NITROIMIDAZOL-1-YL)PENTANOIC ACID - A MODEL FOR POTENTIAL BIOREDUCTIVELY ACTIVATED PRODRUGS FOR INHIBITORS OF NITRIC-OXIDE SYNTHASE (NOS) ACTIVITY
Authors: ULHAQ S NAYLOR MA CHINJE EC THREADGILL MD STRATFORD IJ
Citation: S. Ulhaq et al., S-2-AMINO-5-(2-NITROIMIDAZOL-1-YL)PENTANOIC ACID - A MODEL FOR POTENTIAL BIOREDUCTIVELY ACTIVATED PRODRUGS FOR INHIBITORS OF NITRIC-OXIDE SYNTHASE (NOS) ACTIVITY, Anti-cancer drug design, 12(1), 1997, pp. 61-65
REACTION OF HYDRAZINOQUINOLINES WITH TRIFLUOROMETHYL-BETA-DIKETONES -STRUCTURAL AND MECHANISTIC STUDIES
Authors: SINGH SP KAPOOR JK KUMAR D THREADGILL MD
Citation: Sp. Singh et al., REACTION OF HYDRAZINOQUINOLINES WITH TRIFLUOROMETHYL-BETA-DIKETONES -STRUCTURAL AND MECHANISTIC STUDIES, Journal of fluorine chemistry, 83(1), 1997, pp. 73-79
UPTAKE AND RETENTION OF NITROIMIDAZOLE-CARBORANES DESIGNED FOR BORON NEUTRON-CAPTURE THERAPY IN EXPERIMENTAL MURINE TUMORS - DETECTION BY B-11 MAGNETIC-RESONANCE SPECTROSCOPY
Authors: WOOD PJ SCOBIE M THREADGILL MD
Citation: Pj. Wood et al., UPTAKE AND RETENTION OF NITROIMIDAZOLE-CARBORANES DESIGNED FOR BORON NEUTRON-CAPTURE THERAPY IN EXPERIMENTAL MURINE TUMORS - DETECTION BY B-11 MAGNETIC-RESONANCE SPECTROSCOPY, International journal of radiation biology, 70(5), 1996, pp. 587-592
LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .6. ISOTOPICALLY EFFICIENT SYNTHESES OF [N-15]-NITROTHIOPHENECARBOXAMIDES
Authors: SHINKWIN AE THREADGILL MD
Citation: Ae. Shinkwin et Md. Threadgill, LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .6. ISOTOPICALLY EFFICIENT SYNTHESES OF [N-15]-NITROTHIOPHENECARBOXAMIDES, Journal of labelled compounds & radiopharmaceuticals, 38(11), 1996, pp. 1015-1020
LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .5. SYNTHESES OF [O-18]-5-METHYLISOQUINOLINONE AND 1-(FURAN-2-YL-[O-18]-METHOXY)-5-METHYLISOQUINOLINE
Authors: BERRY JM THREADGILL MD
Citation: Jm. Berry et Md. Threadgill, LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .5. SYNTHESES OF [O-18]-5-METHYLISOQUINOLINONE AND 1-(FURAN-2-YL-[O-18]-METHOXY)-5-METHYLISOQUINOLINE, Journal of labelled compounds & radiopharmaceuticals, 38(10), 1996, pp. 935-940
SYNTHESIS OF A SERIES OF TRIFLUOROMETHYLAZOLES AND DETERMINATION OF PK(A) OF ACIDIC AND BASIC TRIFLUOROMETHYL HETEROCYCLES BY F-19 NMR-SPECTROSCOPY
Authors: JONES BG BRANCH SK THOMSON AS THREADGILL MD
Citation: Bg. Jones et al., SYNTHESIS OF A SERIES OF TRIFLUOROMETHYLAZOLES AND DETERMINATION OF PK(A) OF ACIDIC AND BASIC TRIFLUOROMETHYL HETEROCYCLES BY F-19 NMR-SPECTROSCOPY, Journal of the Chemical Society. Perkin transactions. I, (22), 1996, pp. 2685-2691
MACROMOLECULAR SYSTEMS FOR CHEMOTHERAPY AND MAGNETIC-RESONANCE-IMAGING
Authors: MATTHEWS SE POUTON CW THREADGILL MD
Citation: Se. Matthews et al., MACROMOLECULAR SYSTEMS FOR CHEMOTHERAPY AND MAGNETIC-RESONANCE-IMAGING, Advanced drug delivery reviews, 18(2), 1996, pp. 219-267
SUBSTITUTED FLAVONES AS ARYL-HYDROCARBON (AH) RECEPTOR AGONISTS AND ANTAGONISTS
Authors: LU YF SANTOSTEFANO M CUNNINGHAM BDM THREADGILL MD SAFE S
Citation: Yf. Lu et al., SUBSTITUTED FLAVONES AS ARYL-HYDROCARBON (AH) RECEPTOR AGONISTS AND ANTAGONISTS, Biochemical pharmacology, 51(8), 1996, pp. 1077-1087
MONOFUNCTIONAL ELECTROPHILIC AND NUCLEOPHILIC DERIVATIVES OF MESO-TETRAPHENYLPORPHYRIN FOR ATTACHMENT TO PEPTIDES
Authors: MATTHEWS SE POUTON CW THREADGILL MD
Citation: Se. Matthews et al., MONOFUNCTIONAL ELECTROPHILIC AND NUCLEOPHILIC DERIVATIVES OF MESO-TETRAPHENYLPORPHYRIN FOR ATTACHMENT TO PEPTIDES, Journal of the Chemical Society, Chemical Communications, (17), 1995, pp. 1809-1811
UNEXPECTED FORMATION OF A 5-TRIFLUOROMETHYLOXAZOLE FROM A 1,2-DIBENZAMIDOALKENE
Authors: JONES BG BRANCH SK THREADGILL MD WILMAN DEV
Citation: Bg. Jones et al., UNEXPECTED FORMATION OF A 5-TRIFLUOROMETHYLOXAZOLE FROM A 1,2-DIBENZAMIDOALKENE, Journal of fluorine chemistry, 74(2), 1995, pp. 221-222
INHIBITION OF NITRIC-OXIDE (NO-ASTERISK) PRODUCTION IN MURINE MACROPHAGES BY FLAVONES
Authors: KROL W CZUBA ZP THREADGILL MD CUNNINGHAM BDM PIETSZ G
Citation: W. Krol et al., INHIBITION OF NITRIC-OXIDE (NO-ASTERISK) PRODUCTION IN MURINE MACROPHAGES BY FLAVONES, Biochemical pharmacology, 50(7), 1995, pp. 1031-1035
MODULATION OF LUMINOL-DEPENDENT CHEMILUMINESCENCE OF MURINE MACROPHAGES BY FLAVONE AND ITS SYNTHETIC DERIVATIVES
Authors: KROL W CZUBA ZP THREADGILL MD CUNNINGHAM BDM SHANI J
Citation: W. Krol et al., MODULATION OF LUMINOL-DEPENDENT CHEMILUMINESCENCE OF MURINE MACROPHAGES BY FLAVONE AND ITS SYNTHETIC DERIVATIVES, Arzneimittel-Forschung, 45(7), 1995, pp. 815-818
IDENTIFICATION OF 3'-METHOXY-4'-NITROFLAVONE AS A PURE ARYL-HYDROCARBON (AH) RECEPTOR ANTAGONIST AND EVIDENCE FOR MORE THAN ONE FORM OF THENUCLEAR AH RECEPTOR IN MCF-7 HUMAN BREAST-CANCER CELLS
Authors: LU YF SANTOSTEFANO M CUNNINGHAM BDM THREADGILL MD SAFE S
Citation: Yf. Lu et al., IDENTIFICATION OF 3'-METHOXY-4'-NITROFLAVONE AS A PURE ARYL-HYDROCARBON (AH) RECEPTOR ANTAGONIST AND EVIDENCE FOR MORE THAN ONE FORM OF THENUCLEAR AH RECEPTOR IN MCF-7 HUMAN BREAST-CANCER CELLS, Archives of biochemistry and biophysics, 316(1), 1995, pp. 470-477
LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .4. DEUTERATION ANDTRITIATION OF A NITROIMIDAZOLE-CARBORANE DESIGNED FOR BNCT
Authors: SCOBIE M BEW SP THREADGILL MD
Citation: M. Scobie et al., LABELED COMPOUNDS OF INTEREST AS ANTITUMOR AGENTS .4. DEUTERATION ANDTRITIATION OF A NITROIMIDAZOLE-CARBORANE DESIGNED FOR BNCT, Journal of labelled compounds & radiopharmaceuticals, 34(9), 1994, pp. 881-885
TUMOR-TARGETED BORANES .1. COUPLING OF CLOSO-CARBORANES TO SUBSTITUTED 2-NITROIMIDAZOLES VIA 1,3-DIPOLAR CYCLOADDITION (VOL 1, PG 203, 1994)
Authors: SCOBIE M MAHON MF THREADGILL MD
Citation: M. Scobie et al., TUMOR-TARGETED BORANES .1. COUPLING OF CLOSO-CARBORANES TO SUBSTITUTED 2-NITROIMIDAZOLES VIA 1,3-DIPOLAR CYCLOADDITION (VOL 1, PG 203, 1994), Journal of the Chemical Society. Perkin transactions. I, (7), 1994, pp. 909-909
TUMOR-TARGETED BORANES .2. COUPLING OF CLOSO-CARBORANES TO SUBSTITUTED 2-NITROIMIDAZOLES VIA 1,3-DIPOLAR CYCLOADDITION
Authors: SCOBIE M MAHON MF THREADGILL MD
Citation: M. Scobie et al., TUMOR-TARGETED BORANES .2. COUPLING OF CLOSO-CARBORANES TO SUBSTITUTED 2-NITROIMIDAZOLES VIA 1,3-DIPOLAR CYCLOADDITION, Journal of the Chemical Society. Perkin transactions. I, (2), 1994, pp. 203-210
TUMOR-TARGETED BORANES .3. SYNTHESIS OF CARBAMATE-LINKED NITROIMIDAZOLYL CARBORANES DESIGNED FOR BORON NEUTRON-CAPTURE THERAPY OF CANCER
Authors: SCOBIE M THREADGILL MD
Citation: M. Scobie et Md. Threadgill, TUMOR-TARGETED BORANES .3. SYNTHESIS OF CARBAMATE-LINKED NITROIMIDAZOLYL CARBORANES DESIGNED FOR BORON NEUTRON-CAPTURE THERAPY OF CANCER, Journal of the Chemical Society. Perkin transactions. I, (15), 1994, pp. 2059-2063
TUMOR-TARGETED BORANES .4. SYNTHESIS OF NITROIMIDAZOLE-CARBORANES WITH POLYETHER-ISOXAZOLE LINKS
Authors: SCOBIE M THREADGILL MD
Citation: M. Scobie et Md. Threadgill, TUMOR-TARGETED BORANES .4. SYNTHESIS OF NITROIMIDAZOLE-CARBORANES WITH POLYETHER-ISOXAZOLE LINKS, Journal of organic chemistry, 59(23), 1994, pp. 7008-7013
UNUSUAL DEUTERIUM-ISOTOPE EFFECT ON THE RETENTION OF FORMAMIDES IN GAS-LIQUID-CHROMATOGRAPHY
Authors: MRAZ J JHEETA P GESCHER A THREADGILL MD
Citation: J. Mraz et al., UNUSUAL DEUTERIUM-ISOTOPE EFFECT ON THE RETENTION OF FORMAMIDES IN GAS-LIQUID-CHROMATOGRAPHY, Journal of chromatography, 641(1), 1993, pp. 194-198
POLY(ADP-RIBOSYLATION) AS TARGET FOR CANCER-CHEMOTHERAPY
Authors: JUDSON IR THREADGILL MD
Citation: Ir. Judson et Md. Threadgill, POLY(ADP-RIBOSYLATION) AS TARGET FOR CANCER-CHEMOTHERAPY, Lancet, 342(8872), 1993, pp. 632-632
THE REACTION OF 1,1,1,5,5,5-HEXAFLUOROPENTANE-2,4-DIONE WITH HYDRAZINES - A REINVESTIGATION
Authors: THREADGILL MD HEER AK JONES BG
Citation: Md. Threadgill et al., THE REACTION OF 1,1,1,5,5,5-HEXAFLUOROPENTANE-2,4-DIONE WITH HYDRAZINES - A REINVESTIGATION, Journal of fluorine chemistry, 65(1-2), 1993, pp. 21-23
Risultati: 1-25 | 26-26