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Results: 1-25 | 26-41 |
Results: 26-41/41
ACCUMULATION OF 5-ETHYL-2'-DEOXYURIDINE AND ITS 5,6-DIHYDRO PRODRUGS IN MURINE LUNG AND ITS POTENTIAL CLINICAL-APPLICATION
Authors: CHERAGHALI AM MORIN KW KUMAR R KNAUS EE WIEBE LI
Citation: Am. Cheraghali et al., ACCUMULATION OF 5-ETHYL-2'-DEOXYURIDINE AND ITS 5,6-DIHYDRO PRODRUGS IN MURINE LUNG AND ITS POTENTIAL CLINICAL-APPLICATION, Journal of Pharmacy and Pharmacology, 47(7), 1995, pp. 595-600
THE CYTOSTATIC ACTIVITY OF 5-(1-AZIDOVINYL)-2'-DEOXYURIDINE (AZVDU) AGAINST HERPES-SIMPLEX VIRUS THYMIDINE KINASE GENE-TRANSFECTED FM3A CELLS IS DUE TO INHIBITION OF THYMIDYLATE SYNTHASE AND ENHANCED BY UV-LIGHT (LAMBDA=254 NM) EXPOSURE
Authors: BALZARINI J ANDREI G KUMAR R KNAUS EE WIEBE LI DECLERCQ E
Citation: J. Balzarini et al., THE CYTOSTATIC ACTIVITY OF 5-(1-AZIDOVINYL)-2'-DEOXYURIDINE (AZVDU) AGAINST HERPES-SIMPLEX VIRUS THYMIDINE KINASE GENE-TRANSFECTED FM3A CELLS IS DUE TO INHIBITION OF THYMIDYLATE SYNTHASE AND ENHANCED BY UV-LIGHT (LAMBDA=254 NM) EXPOSURE, FEBS letters, 373(1), 1995, pp. 41-44
THE SYNTHESIS OF N-ACETYL-4-S-CYSTEAMINYL [U-C-14]PHENOL AS A BASIS FOR THE DEVELOPMENT OF AN ANTIMELANOMA AND MELANOMA-RADIOIMAGING AGENT
Authors: IWASHINA T JIMBOW K WIEBE LI
Citation: T. Iwashina et al., THE SYNTHESIS OF N-ACETYL-4-S-CYSTEAMINYL [U-C-14]PHENOL AS A BASIS FOR THE DEVELOPMENT OF AN ANTIMELANOMA AND MELANOMA-RADIOIMAGING AGENT, Applied radiation and isotopes, 45(6), 1994, pp. 703-705
AN EVALUATION OF I-123 IODOAZOMYCINARABINOSIDE AS A MARKER OF LOCALIZED TISSUE HYPOXIA IN PATIENTS WITH DIABETES-MELLITUS
Authors: ALARAFAJ A RYAN EA HUTCHISON K MANNAN RH MERCER J WIEBE LI MCEWAN AJB
Citation: A. Alarafaj et al., AN EVALUATION OF I-123 IODOAZOMYCINARABINOSIDE AS A MARKER OF LOCALIZED TISSUE HYPOXIA IN PATIENTS WITH DIABETES-MELLITUS, European journal of nuclear medicine, 21(12), 1994, pp. 1338-1342
BIOAVAILABILITY AND PHARMACOKINETIC PARAMETERS FOR 5-ETHYL-2'-DEOXYURIDINE
Authors: CHERAGHALI AM KNAUS EE WIEBE LI
Citation: Am. Cheraghali et al., BIOAVAILABILITY AND PHARMACOKINETIC PARAMETERS FOR 5-ETHYL-2'-DEOXYURIDINE, Antiviral research, 25(3-4), 1994, pp. 259-267
SYNTHESIS, IN-VITRO BIOLOGICAL STABILITY, AND ANTI-HIV ACTIVITY OF 6-HALO-6-ALKOXY(OR AZIDO)-5,6-DIHYDRO-3'-AZIDO-3'-DEOXYTHYMIDINE DIASTEREOMERS AS POTENTIAL PRODRUGS TO 3'-AZIDO-3'-DEOXYTHYMIDINE (AZT)
Authors: KUMAR R WANG LL WIEBE LI KNAUS EE
Citation: R. Kumar et al., SYNTHESIS, IN-VITRO BIOLOGICAL STABILITY, AND ANTI-HIV ACTIVITY OF 6-HALO-6-ALKOXY(OR AZIDO)-5,6-DIHYDRO-3'-AZIDO-3'-DEOXYTHYMIDINE DIASTEREOMERS AS POTENTIAL PRODRUGS TO 3'-AZIDO-3'-DEOXYTHYMIDINE (AZT), Journal of medicinal chemistry, 37(25), 1994, pp. 4297-4306
SYNTHESIS AND ANTIVIRAL (HIV-1, HBV) ACTIVITIES OF (OR-AZIDO)-5,6-DIHYDRO-3'-FLUORO-3'-DEOXYTHYMIDINE DIASTEREOMERS - POTENTIAL PRODRUGS TO3'-FLUORO-3'-DEOXYTHYMIDINE
Authors: KUMAR R WANG L WIEBE LI KNAUS EE
Citation: R. Kumar et al., SYNTHESIS AND ANTIVIRAL (HIV-1, HBV) ACTIVITIES OF (OR-AZIDO)-5,6-DIHYDRO-3'-FLUORO-3'-DEOXYTHYMIDINE DIASTEREOMERS - POTENTIAL PRODRUGS TO3'-FLUORO-3'-DEOXYTHYMIDINE, Journal of medicinal chemistry, 37(21), 1994, pp. 3554-3560
A MILD AND EFFICIENT METHODOLOGY FOR THE SYNTHESIS OF 5-HALOGENO URACIL NUCLEOSIDES THAT OCCURS VIA A 5-HALOGENO-6-AZIDO-5,6-DIHYDRO INTERMEDIATE
Authors: KUMAR R WIEBE LI KNAUS EE
Citation: R. Kumar et al., A MILD AND EFFICIENT METHODOLOGY FOR THE SYNTHESIS OF 5-HALOGENO URACIL NUCLEOSIDES THAT OCCURS VIA A 5-HALOGENO-6-AZIDO-5,6-DIHYDRO INTERMEDIATE, Canadian journal of chemistry, 72(9), 1994, pp. 2005-2010
ALPHA-TRIFLUOROMETHYL-BETA-ALANYL GLYCINE (F(3)MBAG) - A NOVEL MAMMALIAN METABOLITE OF TRIFLURIDINE (F(3)TDR)
Authors: TANDON M KUMAR P WIEBE LI
Citation: M. Tandon et al., ALPHA-TRIFLUOROMETHYL-BETA-ALANYL GLYCINE (F(3)MBAG) - A NOVEL MAMMALIAN METABOLITE OF TRIFLURIDINE (F(3)TDR), Biochemical pharmacology, 48(5), 1994, pp. 1033-1041
SYNTHESIS, BIOTRANSFORMATION, PHARMACOKINETICS, AND ANTIVIRAL PROPERTIES OF ETHYL-5-HALO-6-METHOXY-5,6-DIHYDRO-2'-DEOXYURIDINE DIASTEREOMERS
Authors: CHERAGHALI AM KUMAR R WANG L KNAUS EE WIEBE LI
Citation: Am. Cheraghali et al., SYNTHESIS, BIOTRANSFORMATION, PHARMACOKINETICS, AND ANTIVIRAL PROPERTIES OF ETHYL-5-HALO-6-METHOXY-5,6-DIHYDRO-2'-DEOXYURIDINE DIASTEREOMERS, Biochemical pharmacology, 47(9), 1994, pp. 1615-1625
SYNTHESIS OF HYDROPYRIDYL-3-CARBONYL)-2'-FLUORO-2'-DEOXYURIDINE (IVFRU-CDS) FOR BRAIN TARGETED DELIVERY OF IVFRU, AN ANTIVIRAL NUCLEOSIDE
Authors: KUMAR R KNAUS EE WIEBE LI
Citation: R. Kumar et al., SYNTHESIS OF HYDROPYRIDYL-3-CARBONYL)-2'-FLUORO-2'-DEOXYURIDINE (IVFRU-CDS) FOR BRAIN TARGETED DELIVERY OF IVFRU, AN ANTIVIRAL NUCLEOSIDE, Nucleosides & nucleotides, 12(9), 1993, pp. 895-904
ALPHA-TRIFLUOROMETHYL-BETA-UREIDO-PROPIONIC ACID (F3MUPA) - A NEW METABOLITE OF TRIFLURIDINE (F3TDR)
Authors: TANDON M KUMAR P WIEBE LI
Citation: M. Tandon et al., ALPHA-TRIFLUOROMETHYL-BETA-UREIDO-PROPIONIC ACID (F3MUPA) - A NEW METABOLITE OF TRIFLURIDINE (F3TDR), Nucleosides & nucleotides, 12(8), 1993, pp. 803-814
SYNTHESIS AND ANTIVIRAL ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLURACILS AND URIDINES CONTAINING 5-[2-BROMO-2-CHLORO (OR BROMO)-1-HYDROXY (OR METHOXY) ETHYL] SUBSTITUENTS
Authors: KUMAR R WIEBE LI KNAUS EE
Citation: R. Kumar et al., SYNTHESIS AND ANTIVIRAL ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLURACILS AND URIDINES CONTAINING 5-[2-BROMO-2-CHLORO (OR BROMO)-1-HYDROXY (OR METHOXY) ETHYL] SUBSTITUENTS, Nucleosides & nucleotides, 12(5), 1993, pp. 537-545
IMAGING TUMOR HYPOXIA AND TUMOR PERFUSION
Authors: GROSHAR D MCEWAN AJB PARLIAMENT MB URTASUN RC GOLBERG LE HOSKINSON M MERCER JR MANNAN RH WIEBE LI CHAPMAN JD
Citation: D. Groshar et al., IMAGING TUMOR HYPOXIA AND TUMOR PERFUSION, The Journal of nuclear medicine, 34(6), 1993, pp. 885-888
SYNTHESIS AND ANTIVIRAL ACTIVITY OF NOVEL 5-(1-AZIDO-2-HALOETHYL) AND5-(1-AZIDOETHYL, AMINOETHYL, OR METHOXYETHYL) ANALOGS OF 2'-DEOXYURIDINE
Authors: KUMAR R WIEBE LI KNAUS EE
Citation: R. Kumar et al., SYNTHESIS AND ANTIVIRAL ACTIVITY OF NOVEL 5-(1-AZIDO-2-HALOETHYL) AND5-(1-AZIDOETHYL, AMINOETHYL, OR METHOXYETHYL) ANALOGS OF 2'-DEOXYURIDINE, Journal of medicinal chemistry, 36(17), 1993, pp. 2470-2474
SYNTHESIS OF BRAIN-TARGETED RO-BETA-D-RIBOFURANOSYL)-(E)-5-(2-IODOVINYL)URACIL COUPLED TO A DIHYDROPYRIDINE REVERSIBLE-ARROW PYRIDINIUM SALT REDOX CHEMICAL-DELIVERY SYSTEM
Authors: MORIN KW WIEBE LI KNAUS EE
Citation: Kw. Morin et al., SYNTHESIS OF BRAIN-TARGETED RO-BETA-D-RIBOFURANOSYL)-(E)-5-(2-IODOVINYL)URACIL COUPLED TO A DIHYDROPYRIDINE REVERSIBLE-ARROW PYRIDINIUM SALT REDOX CHEMICAL-DELIVERY SYSTEM, Carbohydrate research, 249(1), 1993, pp. 109-116
Risultati: 1-25 | 26-41 |