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Results: 1-18 |
Results: 18
RATIONAL DESIGN AND SYNTHESIS OF PHENETHYL-5-BROMOPYRIDYL THIOUREA DERIVATIVES AS POTENT NONNUCLEOSIDE INHIBITORS OF HIV REVERSE-TRANSCRIPTASE
Authors: VIG R MAO C VENKATACHALAM TK TUELAHLGREN L SUDBECK EA UCKUN FM
Citation: R. Vig et al., RATIONAL DESIGN AND SYNTHESIS OF PHENETHYL-5-BROMOPYRIDYL THIOUREA DERIVATIVES AS POTENT NONNUCLEOSIDE INHIBITORS OF HIV REVERSE-TRANSCRIPTASE, Bioorganic & medicinal chemistry, 6(10), 1998, pp. 1789-1797
STRUCTURE-BASED DESIGN OF PIPERIDINYLETHYL)]-N'-[2-(5-BROMOPYRIDYL]-THIOUREA AND IPERAZINYLETHYL)]-N'-[2-(5-BROMOPYRIDYL)]-THIOUREA AS POTENT NONNUCLEOSIDE INHIBITORS OF HIV-1 REVERSE-TRANSCRIPTASE
Authors: MAO C VIG R VENKATACHALAM TK SUDBECK EA UCKUN FM
Citation: C. Mao et al., STRUCTURE-BASED DESIGN OF PIPERIDINYLETHYL)]-N'-[2-(5-BROMOPYRIDYL]-THIOUREA AND IPERAZINYLETHYL)]-N'-[2-(5-BROMOPYRIDYL)]-THIOUREA AS POTENT NONNUCLEOSIDE INHIBITORS OF HIV-1 REVERSE-TRANSCRIPTASE, Bioorganic & medicinal chemistry letters, 8(16), 1998, pp. 2213-2218
LTHIOMETHYL)THIO]-6-(BENZYL)-PYRIMIDIN-4-(1H)-ONES AS POTENT NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS OF S-DABO SERIES
Authors: VIG R MAO C VENKATACHALAM TK TUELAHLGREN L SUDBECK EA UCKUN FM
Citation: R. Vig et al., LTHIOMETHYL)THIO]-6-(BENZYL)-PYRIMIDIN-4-(1H)-ONES AS POTENT NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS OF S-DABO SERIES, Bioorganic & medicinal chemistry letters, 8(12), 1998, pp. 1461-1466
ARYL PHOSPHATE DERIVATIVES OF 3'-DEOXYTHYMIDINE ARE NOT POTENT ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENTS
Authors: VIG R VENKATACHALAM TK JAN ST UCKUN FM
Citation: R. Vig et al., ARYL PHOSPHATE DERIVATIVES OF 3'-DEOXYTHYMIDINE ARE NOT POTENT ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENTS, Antiviral chemistry & chemotherapy, 9(5), 1998, pp. 439-443
D4T-5'-[P-BROMOPHENYL METHOXYALANINYL PHOSPHATE] AS A POTENT AND NONTOXIC ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENT
Authors: VIG R VENKATACHALAM TK UCKUN FM
Citation: R. Vig et al., D4T-5'-[P-BROMOPHENYL METHOXYALANINYL PHOSPHATE] AS A POTENT AND NONTOXIC ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENT, Antiviral chemistry & chemotherapy, 9(5), 1998, pp. 445-448
THE ENZYMATIC SULFATION OF GLYCOPROTEIN CARBOHYDRATE UNITS - BLOOD-GROUP T-HAPTEN SPECIFIC AND 2 OTHER DISTINCT GAL-3-O-SULFOTRANSFERASES AS EVIDENT FROM SPECIFICITIES AND KINETICS AND THE INFLUENCE OF SULFATEAND FUCOSE RESIDUES OCCURRING IN THE CARBOHYDRATE CHAIN ON C-3 SULFATION OF TERMINAL GAL
Authors: CHANDRASEKARAN EV JAIN RK VIG R MATTA KL
Citation: Ev. Chandrasekaran et al., THE ENZYMATIC SULFATION OF GLYCOPROTEIN CARBOHYDRATE UNITS - BLOOD-GROUP T-HAPTEN SPECIFIC AND 2 OTHER DISTINCT GAL-3-O-SULFOTRANSFERASES AS EVIDENT FROM SPECIFICITIES AND KINETICS AND THE INFLUENCE OF SULFATEAND FUCOSE RESIDUES OCCURRING IN THE CARBOHYDRATE CHAIN ON C-3 SULFATION OF TERMINAL GAL, Glycobiology, 7(6), 1997, pp. 753-768
SELECTIN INHIBITION - SYNTHESIS AND EVALUATION OF NOVEL SIALYLATED, SULFATED AND FUCOSYLATED OLIGOSACCHARIDES, INCLUDING THE MAJOR CAPPING GROUP OF GLYCAM-1
Authors: KOENIG A JAIN R VIG R NORGARDSUMNICHT KE MATTA KL VARKI A
Citation: A. Koenig et al., SELECTIN INHIBITION - SYNTHESIS AND EVALUATION OF NOVEL SIALYLATED, SULFATED AND FUCOSYLATED OLIGOSACCHARIDES, INCLUDING THE MAJOR CAPPING GROUP OF GLYCAM-1, Glycobiology, 7(1), 1997, pp. 79-93
MONOLITHIC MAGNETIC HALL SENSOR USING DYNAMIC QUADRATURE OFFSET CANCELLATION
Authors: BILOTTI A MONREAL G VIG R
Citation: A. Bilotti et al., MONOLITHIC MAGNETIC HALL SENSOR USING DYNAMIC QUADRATURE OFFSET CANCELLATION, IEEE journal of solid-state circuits, 32(6), 1997, pp. 829-836
SELECTIN LIGANDS - 2,3,4-TRI-O-ACETYL-6-O-PIVALOYL-ALPHA BETA-GALACTOPYRANOSYL HALIDE AS NOVEL GLYCOSYL DONOR FOR THE SYNTHESIS OF 3-O-SIALYL OR 3-O-SULFO LE(X) AND LE(A) TYPE STRUCTURES/
Authors: JAIN RK VIG R LOCKE RD MOHAMMAD A MATTA KL
Citation: Rk. Jain et al., SELECTIN LIGANDS - 2,3,4-TRI-O-ACETYL-6-O-PIVALOYL-ALPHA BETA-GALACTOPYRANOSYL HALIDE AS NOVEL GLYCOSYL DONOR FOR THE SYNTHESIS OF 3-O-SIALYL OR 3-O-SULFO LE(X) AND LE(A) TYPE STRUCTURES/, Chemical communications, (1), 1996, pp. 65-67
NUCLEOSIDE CONJUGATES .15. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF ANTI-HIV NUCLEOSIDE CONJUGATES OF ETHER AND THIOETHER PHOSPHOLIPIDS
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R WEST CR MANOUILOV KK CHU CK
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .15. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF ANTI-HIV NUCLEOSIDE CONJUGATES OF ETHER AND THIOETHER PHOSPHOLIPIDS, Journal of medicinal chemistry, 39(9), 1996, pp. 1771-1777
SELECTIN LIGANDS - SYNTHESIS OF 3'-O-SIALYL-6'-O-SULFO LEWIS(A), NEUAC-ALPHA-2-]3(6-O-SO3NA)GAL-BETA-1-]3 (FUC-ALPHA-1-]4) GLCNAC-BETA-OME
Authors: VIG R JAIN RK PISKORZ CF MATTA KL
Citation: R. Vig et al., SELECTIN LIGANDS - SYNTHESIS OF 3'-O-SIALYL-6'-O-SULFO LEWIS(A), NEUAC-ALPHA-2-]3(6-O-SO3NA)GAL-BETA-1-]3 (FUC-ALPHA-1-]4) GLCNAC-BETA-OME, Journal of the Chemical Society, Chemical Communications, (20), 1995, pp. 2073-2074
NUCLEOSIDE CONJUGATES .14. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF ETHER LIPIDS WITH IMPROVED WATER SOLUBILITY
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R HUI SW WEST CR
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .14. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF ETHER LIPIDS WITH IMPROVED WATER SOLUBILITY, Journal of medicinal chemistry, 38(10), 1995, pp. 1629-1634
SYNTHESIS OF METHYL ACETAMIDO-2-DEOXY-6-O-SULFO-BETA-D-GLUCOPYRANOSIDE SODIUM-SALT AS A POTENTIAL LIGAND FOR SELECTIN MOLECULES (VOL 266, PG 279, 1995)
Authors: VIG R JAIN RK MATTA KL
Citation: R. Vig et al., SYNTHESIS OF METHYL ACETAMIDO-2-DEOXY-6-O-SULFO-BETA-D-GLUCOPYRANOSIDE SODIUM-SALT AS A POTENTIAL LIGAND FOR SELECTIN MOLECULES (VOL 266, PG 279, 1995), Carbohydrate research, 272(1), 1995, pp. 3-3
SYNTHESIS OF METHYL ACETAMIDO-2-DEOXY-6-O-SULFO-BETA-D-GLUCOPYRANOSIDE SODIUM-SALT AS A POTENTIAL LIGAND FOR SELECTIN MOLECULES
Authors: VIG R JAIN RK MATTA KL
Citation: R. Vig et al., SYNTHESIS OF METHYL ACETAMIDO-2-DEOXY-6-O-SULFO-BETA-D-GLUCOPYRANOSIDE SODIUM-SALT AS A POTENTIAL LIGAND FOR SELECTIN MOLECULES, Carbohydrate research, 266(2), 1995, pp. 279-284
TOTAL SYNTHESIS OF 3'-O-SIALYL, 6'-O-SULFO LEWIS(X), O3NA)GA1-BETA-1-]4(FUC-ALPHA-1-]3)-GLCNAC-BETA-OME - A MAJOR CAPPING GROUP OF GLYCAM-I
Authors: JAIN RK VIG R RAMPAL R CHANDRASEKARAN EV MATTA KL
Citation: Rk. Jain et al., TOTAL SYNTHESIS OF 3'-O-SIALYL, 6'-O-SULFO LEWIS(X), O3NA)GA1-BETA-1-]4(FUC-ALPHA-1-]3)-GLCNAC-BETA-OME - A MAJOR CAPPING GROUP OF GLYCAM-I, Journal of the American Chemical Society, 116(26), 1994, pp. 12123-12124
SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINECONJUGATES OF OPTICAL ISOMERS OF ETHER AND THIOETHER LIPIDS
Authors: HONG CI AN SH NECHAEV A KIRISITS AJ VIG R WEST CR
Citation: Ci. Hong et al., SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINECONJUGATES OF OPTICAL ISOMERS OF ETHER AND THIOETHER LIPIDS, Lipids, 28(11), 1993, pp. 1021-1026
NUCLEOSIDE CONJUGATES .13. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF THIOETHER LIPIDS WITH IMPROVED WATER SOLUBILITY
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R WEST CR
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .13. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF THIOETHER LIPIDS WITH IMPROVED WATER SOLUBILITY, Journal of medicinal chemistry, 36(12), 1993, pp. 1785-1790
SYNTHESIS OF (E)-9-OXO-2-DECENOIC ACID AND (E)-10-HYDROXY-2-DECENOIC ACID
Authors: TREHEN IR VIG R SINGH V SHARMA S KAD GL
Citation: Ir. Trehen et al., SYNTHESIS OF (E)-9-OXO-2-DECENOIC ACID AND (E)-10-HYDROXY-2-DECENOIC ACID, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 31(4), 1992, pp. 257-259
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