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Results: 1-25 | 26-50 | 51-61
Results: 26-50/61
SYNTHESIS, BIOLOGICAL EVALUATION, CALCIUM-CHANNEL ANTAGONIST ACTIVITY, AND ANTICONVULSANT ACTIVITY OF FELODIPINE COUPLED TO A DIHYDROPYRIDINE-PYRIDINIUM SALT REDOX CHEMICAL DELIVERY SYSTEM
Authors: YIU SH KNAUS EE
Citation: Sh. Yiu et Ee. Knaus, SYNTHESIS, BIOLOGICAL EVALUATION, CALCIUM-CHANNEL ANTAGONIST ACTIVITY, AND ANTICONVULSANT ACTIVITY OF FELODIPINE COUPLED TO A DIHYDROPYRIDINE-PYRIDINIUM SALT REDOX CHEMICAL DELIVERY SYSTEM, Journal of medicinal chemistry, 39(23), 1996, pp. 4576-4582
SYNTHESIS OF 3-(2-GUANIDINOETHYL) AND 3-[2-(S-METHYLISOTHIOUREIDOETHYL)] ANALOGS OF 5-ISOPROPYL -4-(2,3-DICLOROROPHENYL)PYRIDINE-3,5-DICARBOXYLATE AS A RESPECTIVE RELEASER OF NITRIC-OXIDE AND INHIBITOR OF NITRIC-OXIDE SYNTHASE
Authors: IQBAL N KNAUS EE
Citation: N. Iqbal et Ee. Knaus, SYNTHESIS OF 3-(2-GUANIDINOETHYL) AND 3-[2-(S-METHYLISOTHIOUREIDOETHYL)] ANALOGS OF 5-ISOPROPYL -4-(2,3-DICLOROROPHENYL)PYRIDINE-3,5-DICARBOXYLATE AS A RESPECTIVE RELEASER OF NITRIC-OXIDE AND INHIBITOR OF NITRIC-OXIDE SYNTHASE, Journal of heterocyclic chemistry, 33(1), 1996, pp. 157-160
SYNTHESIS OF 5-(1-ARIDOVINYL) AND 5-[2-(1-AZIRINYL)] ANALOGS OF 2'-DEOXYURIDINE
Authors: KUMAR R WIEBE LI KNAUS EE
Citation: R. Kumar et al., SYNTHESIS OF 5-(1-ARIDOVINYL) AND 5-[2-(1-AZIRINYL)] ANALOGS OF 2'-DEOXYURIDINE, Canadian journal of chemistry, 74(9), 1996, pp. 1609-1615
NITRIC-OXIDE, A POSSIBLE MEDIATOR OF 1,4-DIHYDROPYRIDINE-INDUCED PHOTORELAXATION OF VASCULAR SMOOTH-MUSCLE
Authors: LOVREN F ONEILL SK BIEGER D IGBAL N KNAUS EE TRIGGLE CR
Citation: F. Lovren et al., NITRIC-OXIDE, A POSSIBLE MEDIATOR OF 1,4-DIHYDROPYRIDINE-INDUCED PHOTORELAXATION OF VASCULAR SMOOTH-MUSCLE, British Journal of Pharmacology, 118(4), 1996, pp. 879-884
NOVEL (E)-5-(2-IODOVINYL)-2'-DEOXYURIDINE DERIVATIVES AS POTENTIAL CYTOSTATIC AGENTS AGAINST HERPES-SIMPLEX VIRUS THYMIDINE KINASE GENE TRANSFECTED TUMORS
Authors: BALZARINI J MORIN KW KNAUS EE WIEBE LI DECLERCQ E
Citation: J. Balzarini et al., NOVEL (E)-5-(2-IODOVINYL)-2'-DEOXYURIDINE DERIVATIVES AS POTENTIAL CYTOSTATIC AGENTS AGAINST HERPES-SIMPLEX VIRUS THYMIDINE KINASE GENE TRANSFECTED TUMORS, Gene therapy, 2(5), 1995, pp. 317-322
A COMPARATIVE-STUDY OF 5-ETHYL-2'-DEOXYURIDINE AND SELECTED LIPOPHILIC 5,6-DIHYDRO DOUBLE TRIPLE PRODRUGS
Authors: CHERAGHALI AM KUMAR R MORIN KW DECLERCQ E KNAUS EE WIEBE LI
Citation: Am. Cheraghali et al., A COMPARATIVE-STUDY OF 5-ETHYL-2'-DEOXYURIDINE AND SELECTED LIPOPHILIC 5,6-DIHYDRO DOUBLE TRIPLE PRODRUGS, Antiviral chemistry & chemotherapy, 6(6), 1995, pp. 356-364
5-HALO-6-ALKOXY-5,6-DIHYDRO-PYRIMIDINE NUCLEOSIDES - ANTIVIRAL NUCLEOSIDES OR NUCLEOSIDE PRODRUGS
Authors: WIEBE LI KNAUS EE CHERAGHALI AM KUMAR R MORIN KW WANG L
Citation: Li. Wiebe et al., 5-HALO-6-ALKOXY-5,6-DIHYDRO-PYRIMIDINE NUCLEOSIDES - ANTIVIRAL NUCLEOSIDES OR NUCLEOSIDE PRODRUGS, Nucleosides & nucleotides, 14(3-5), 1995, pp. 501-505
SYNTHESIS AND CALCIUM-CHANNEL MODULATING EFFECTS OF ALKYL 1,4-DIHYDRO-2,6-DIMETHYL-4-(PYRIDINYL OR HENYL)-5-(1H-TETRAZOL-5-YL)-3-PYRIDINECARBOXYLATES
Authors: IQBAL N KNAUS EE
Citation: N. Iqbal et Ee. Knaus, SYNTHESIS AND CALCIUM-CHANNEL MODULATING EFFECTS OF ALKYL 1,4-DIHYDRO-2,6-DIMETHYL-4-(PYRIDINYL OR HENYL)-5-(1H-TETRAZOL-5-YL)-3-PYRIDINECARBOXYLATES, Archiv der pharmazie, 328(11-12), 1995, pp. 750-754
PHARMACOKINETICS AND BIOAVAILABILITY OF 5-ETHYL-2'-DEOXYURIDINE AND ITS NOVEL (5R,6R)-5-BROMO-6-ETHOXY-5,6-DIHYDRO PRODRUGS IN MICE
Authors: CHERAGHALI AM KUMAR R KNAUS EE WIEBE LI
Citation: Am. Cheraghali et al., PHARMACOKINETICS AND BIOAVAILABILITY OF 5-ETHYL-2'-DEOXYURIDINE AND ITS NOVEL (5R,6R)-5-BROMO-6-ETHOXY-5,6-DIHYDRO PRODRUGS IN MICE, Drug metabolism and disposition, 23(2), 1995, pp. 223-226
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
SYNTHESES, CALCIUM-CHANNEL AGONIST-ANTAGONIST MODULATION ACTIVITIES, AND VOLTAGE-CLAMP STUDIES OF ISOPROPYL DIMETHYL-3-NITRO-4-PYRIDINYLPYRIDINE-5-CARBOXYLATE RACEMATES AND ENANTIOMERS
Authors: VO D MATOWE WC RAMESH M IQBAL N WOLOWYK MW HOWLETT SE KNAUS EE
Citation: D. Vo et al., SYNTHESES, CALCIUM-CHANNEL AGONIST-ANTAGONIST MODULATION ACTIVITIES, AND VOLTAGE-CLAMP STUDIES OF ISOPROPYL DIMETHYL-3-NITRO-4-PYRIDINYLPYRIDINE-5-CARBOXYLATE RACEMATES AND ENANTIOMERS, Journal of medicinal chemistry, 38(15), 1995, pp. 2851-2859
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
ONE-STEP REDUCTION-WITTIG OLEFINATION OF METHYL PYROGLUTAMATE - CHIRAL SYNTHESES OF (5S)-5-ALKENYL-2-PYRROLIDINONES AND (S)-VIGABATRIN(R)
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, ONE-STEP REDUCTION-WITTIG OLEFINATION OF METHYL PYROGLUTAMATE - CHIRAL SYNTHESES OF (5S)-5-ALKENYL-2-PYRROLIDINONES AND (S)-VIGABATRIN(R), Synlett, (5), 1994, pp. 345-346
ENANTIOSELECTIVE SYNTHESES AND CALCIUM-CHANNEL MODULATING EFFECTS OF (-3-ISOPROPYL AND (-)-3-ISOPROPYL 5-(4-METHYLPHENETHYL) METHYL-4-(2-PYRIDYL)-3,5-PYRIDINEDICARBOXYLATES())
Authors: IQBAL N VO D MCEWEN CA WOLOWYK MW KNAUS EE
Citation: N. Iqbal et al., ENANTIOSELECTIVE SYNTHESES AND CALCIUM-CHANNEL MODULATING EFFECTS OF (-3-ISOPROPYL AND (-)-3-ISOPROPYL 5-(4-METHYLPHENETHYL) METHYL-4-(2-PYRIDYL)-3,5-PYRIDINEDICARBOXYLATES()), Chirality, 6(7), 1994, pp. 515-520
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 OF 5-[1-HYDROXY (OR METHOXY)-2,2-DIHALOETHYL]-2'-DEOXYURIDINES WITH ANTIVIRAL AND CYTOTOXIC ACTIVITY
Authors: KUMAR R KNAUS EE WIEBE LF ALLEN TM
Citation: R. Kumar et al., SYNTHESIS OF 5-[1-HYDROXY (OR METHOXY)-2,2-DIHALOETHYL]-2'-DEOXYURIDINES WITH ANTIVIRAL AND CYTOTOXIC ACTIVITY, Antiviral research, 24(4), 1994, pp. 315-325
A MECHANISM-BASED CLEAVAGE OF LACTAM-CARBAMATES
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, A MECHANISM-BASED CLEAVAGE OF LACTAM-CARBAMATES, Tetrahedron letters, 35(6), 1994, pp. 847-848
A REGIOSELECTIVE TANDEM REDUCTION - WITTIG-HORNER REACTION INVOLVING THE ALPHA-ESTER MOIETY OF DIETHYL ASPARTATE OR GLUTAMATE
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, A REGIOSELECTIVE TANDEM REDUCTION - WITTIG-HORNER REACTION INVOLVING THE ALPHA-ESTER MOIETY OF DIETHYL ASPARTATE OR GLUTAMATE, Tetrahedron letters, 35(15), 1994, pp. 2305-2308
ASYMMETRIC-SYNTHESIS OF BOTH ENANTIOMERS OF VIGABATRIN(R) - AN APPROACH USING METHIONINE AS THE CHIRAL POOL
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, ASYMMETRIC-SYNTHESIS OF BOTH ENANTIOMERS OF VIGABATRIN(R) - AN APPROACH USING METHIONINE AS THE CHIRAL POOL, Tetrahedron, 50(19), 1994, pp. 5569-5578
IMPROVED SYNTHESIS OF CHIRAL N-PROTECTED ALLYLIC AMINES
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, IMPROVED SYNTHESIS OF CHIRAL N-PROTECTED ALLYLIC AMINES, Synthesis, (12), 1994, pp. 1463-1466
RESOLUTION OF 5-VINYL-2-PYRROLIDINONE - A PRACTICAL SYNTHESIS OF (S)-VIGABATRIN AND (R)-VIGABATRIN
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, RESOLUTION OF 5-VINYL-2-PYRROLIDINONE - A PRACTICAL SYNTHESIS OF (S)-VIGABATRIN AND (R)-VIGABATRIN, Organic preparations and procedures international, 26(5), 1994, pp. 567-570
AN EFFICIENT ONE-POT CONVERSION OF ALPHA-AMINO-ACID ESTERS TO GAMMA-AMINO-ALPHA,BETA-UNSATURATED CARBOXYLATES
Authors: WEI ZY KNAUS EE
Citation: Zy. Wei et Ee. Knaus, AN EFFICIENT ONE-POT CONVERSION OF ALPHA-AMINO-ACID ESTERS TO GAMMA-AMINO-ALPHA,BETA-UNSATURATED CARBOXYLATES, Organic preparations and procedures international, 26(2), 1994, pp. 243-248
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
Risultati: 1-25 | 26-50 | 51-61