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Results: 1-9 |
Results: 9
GEOMETRICALLY AND CONFORMATIONALLY RESTRAINED CINNAMOYL COMPOUNDS AS INHIBITORS OF HIV-1 INTEGRASE - SYNTHESIS, BIOLOGICAL EVALUATION, AND MOLECULAR MODELING
Authors: ARTICO M DISANTO R COSTI R NOVELLINO E GRECO G MASSA S TRAMONTANO E MARONGIU ME DEMONTIS A LACOLLA P
Citation: M. Artico et al., GEOMETRICALLY AND CONFORMATIONALLY RESTRAINED CINNAMOYL COMPOUNDS AS INHIBITORS OF HIV-1 INTEGRASE - SYNTHESIS, BIOLOGICAL EVALUATION, AND MOLECULAR MODELING, Journal of medicinal chemistry, 41(21), 1998, pp. 3948-3960
BIOCHEMICAL-CHARACTERIZATION OF THE HIV-1 INTEGRASE 3'-PROCESSING ACTIVITY AND ITS INHIBITION BY PHOSPHOROTHIOATE OLIGONUCLEOTIDES
Authors: TRAMONTANO E LACOLLA P CHENG YC
Citation: E. Tramontano et al., BIOCHEMICAL-CHARACTERIZATION OF THE HIV-1 INTEGRASE 3'-PROCESSING ACTIVITY AND ITS INHIBITION BY PHOSPHOROTHIOATE OLIGONUCLEOTIDES, Biochemistry, 37(20), 1998, pp. 7237-7243
SYNTHESIS AND ANTIVIRAL ACTIVITY OF NEW 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS), SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
Authors: MASSA S MAI A ARTICO M SBARDELLA G TRAMONTANO E LOI AG SCANO P LACOLLA P
Citation: S. Massa et al., SYNTHESIS AND ANTIVIRAL ACTIVITY OF NEW 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS), SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1, Antiviral chemistry & chemotherapy, 6(1), 1995, pp. 1-8
SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF THIO ANALOGS OF DIHYDROALKOXYBENZYLOXOPYRIMIDINES
Authors: MAI A ARTICO M SBARDELLA G MASSA S LOI AG TRAMONTANO E SCANO P LACOLLA P
Citation: A. Mai et al., SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF THIO ANALOGS OF DIHYDROALKOXYBENZYLOXOPYRIMIDINES, Journal of medicinal chemistry, 38(17), 1995, pp. 3258-3263
CHARACTERIZATION OF THE ANTI-HIV-1 ACTIVITY OF 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS), NEW NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS
Authors: TRAMONTANO E MARONGIU ME DEMONTIS A LOI AG ARTICO M MASSA S MAI A LACOLLA P
Citation: E. Tramontano et al., CHARACTERIZATION OF THE ANTI-HIV-1 ACTIVITY OF 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS), NEW NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS, The New microbiologica, 17(4), 1994, pp. 269-279
SYNTHESIS AND EVALUATION OF THE ANTI-HTV ACTIVITY OF AZA AND DEAZA ANALOGS OF ISODDA AND THEIR PHOSPHATES AS PRODRUGS
Authors: FRANCHETTI P CAPPELLACCI L GRIFANTINI M MESSINI L SHEIKHA GA LOI AG TRAMONTANO E DEMONTIS A SPIGA MG LACOLLA P
Citation: P. Franchetti et al., SYNTHESIS AND EVALUATION OF THE ANTI-HTV ACTIVITY OF AZA AND DEAZA ANALOGS OF ISODDA AND THEIR PHOSPHATES AS PRODRUGS, Journal of medicinal chemistry, 37(21), 1994, pp. 3534-3541
3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS) - A NEW CLASS OF SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
Authors: ARTICO M MASSA S MAI A MARONGIU ME PIRAS G TRAMONTANO E LACOLLA P
Citation: M. Artico et al., 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS) - A NEW CLASS OF SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1, Antiviral chemistry & chemotherapy, 4(6), 1993, pp. 361-368
IDENTIFICATION OF THE AMINO-ACID IN THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INVOLVED IN THE PYROPHOSPHATE BINDING OF ANTIVIRAL NUCLEOSIDE TRIPHOSPHATE ANALOGS AND PHOSPHONOFORMATE - IMPLICATIONS FOR MULTIPLE-DRUG RESISTANCE
Authors: IM GJ TRAMONTANO E GONZALEZ CJ CHENG YC
Citation: Gj. Im et al., IDENTIFICATION OF THE AMINO-ACID IN THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INVOLVED IN THE PYROPHOSPHATE BINDING OF ANTIVIRAL NUCLEOSIDE TRIPHOSPHATE ANALOGS AND PHOSPHONOFORMATE - IMPLICATIONS FOR MULTIPLE-DRUG RESISTANCE, Biochemical pharmacology, 46(12), 1993, pp. 2307-2313
INVITRO SELECTION AND MOLECULAR CHARACTERIZATION OF HUMAN IMMUNODEFICIENCY VIRUS-1 RESISTANT TO NONNUCLEOSIDE INHIBITORS OF REVERSE-TRANSCRIPTASE
Authors: MELLORS JW DUTSCHMAN GE IM GJ TRAMONTANO E WINKLER SR CHENG YC
Citation: Jw. Mellors et al., INVITRO SELECTION AND MOLECULAR CHARACTERIZATION OF HUMAN IMMUNODEFICIENCY VIRUS-1 RESISTANT TO NONNUCLEOSIDE INHIBITORS OF REVERSE-TRANSCRIPTASE, Molecular pharmacology, 41(3), 1992, pp. 446-451
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