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Results: 1-22 |
Results: 22
POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE STRUCTURALLY RELATED TO L-694,746
Authors: FRANCHETTI P PERLINI P ABUSHEIKHA G CAPPELLACCI L GRIFANTINI M LOI AG DEMONTIS A PANI A MARONGIU ME LACOLLA P
Citation: P. Franchetti et al., POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE STRUCTURALLY RELATED TO L-694,746, Antiviral chemistry & chemotherapy, 9(4), 1998, pp. 303-309
1,2,5-BENZOTHIADIAZEPINE AND PYRROLO[2,1-D][1,2,5]BENZOTHIADIAZEPINE DERIVATIVES WITH SPECIFIC ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVITY
Authors: DISANTO R COSTI R ARTICO M MASSA S MARONGIU ME LOI AG DEMONTIS A LACOLLA P
Citation: R. Disanto et al., 1,2,5-BENZOTHIADIAZEPINE AND PYRROLO[2,1-D][1,2,5]BENZOTHIADIAZEPINE DERIVATIVES WITH SPECIFIC ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVITY, Antiviral chemistry & chemotherapy, 9(2), 1998, pp. 127-137
SYNTHESIS AND BIOLOGICAL EVALUATION OF 5H-INDOLO[3,2-B][1,5]BENZOTHIAZEPINE DERIVATIVES, DESIGNED AS CONFORMATIONALLY CONSTRAINED ANALOGS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INHIBITOR L-737,126
Authors: SILVESTRI R ARTICO M BRUNO B MASSA S NOVELLINO E GRECO G MARONGIU ME PANI A DEMONTIS A LACOLLA P
Citation: R. Silvestri et al., SYNTHESIS AND BIOLOGICAL EVALUATION OF 5H-INDOLO[3,2-B][1,5]BENZOTHIAZEPINE DERIVATIVES, DESIGNED AS CONFORMATIONALLY CONSTRAINED ANALOGS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE INHIBITOR L-737,126, Antiviral chemistry & chemotherapy, 9(2), 1998, pp. 139-148
IN-VITRO AND IN-VIVO ANTIPROLIFERATIVE ACTIVITY OF IPCAP, A NEW PYRAZOLE NUCLEOSIDE ANALOG
Authors: PANI A MARONGIU ME PINNA E SCINTU F PERRA G DEMONTIS A MANFREDINI S LACOLLA P
Citation: A. Pani et al., IN-VITRO AND IN-VIVO ANTIPROLIFERATIVE ACTIVITY OF IPCAP, A NEW PYRAZOLE NUCLEOSIDE ANALOG, Anticancer research, 18(4A), 1998, pp. 2623-2630
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
-ARYLSULFONYL-3-(ALPHA-HYDROXYBENZYL)-1H-PYRROLES, A NOVEL CLASS OF ANTI-HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS
Authors: ARTICO M DISANTO R COSTI R MASSA S SCINTU F LOI AG DEMONTIS A LACOLLA P
Citation: M. Artico et al., -ARYLSULFONYL-3-(ALPHA-HYDROXYBENZYL)-1H-PYRROLES, A NOVEL CLASS OF ANTI-HIV-1 REVERSE-TRANSCRIPTASE INHIBITORS, Bioorganic & medicinal chemistry letters, 7(14), 1997, pp. 1931-1936
ARYLKETOTETRAMETHYLENE ANALOGS OF DISOXARIL WITH ANTI-HUMAN RHINOVIRUS-14 ACTIVITY
Authors: MAI A ARTICO M SBARDELLA G MASSA S DEMONTIS A PUDDU I MUSIU C LACOLLA P
Citation: A. Mai et al., ARYLKETOTETRAMETHYLENE ANALOGS OF DISOXARIL WITH ANTI-HUMAN RHINOVIRUS-14 ACTIVITY, Antiviral chemistry & chemotherapy, 8(3), 1997, pp. 235-242
SYNTHESIS, STRUCTURE, AND ANTIPROLIFERATIVE ACTIVITY OF SELENOPHENFURIN, AN INOSINE 5'-MONOPHOSPHATE DEHYDROGENASE INHIBITOR ANALOG OF SELENAZOFURIN
Authors: FRANCHETTI P CAPPELLACCI L ABUSHEIKHA G JAYARAM HN GURUDUTT VV SINT T SCHNEIDER BP JONES WD GOLDSTEIN BM PERRA G DEMONTIS A LOI AG LACOLLA P GRIFANTINI M
Citation: P. Franchetti et al., SYNTHESIS, STRUCTURE, AND ANTIPROLIFERATIVE ACTIVITY OF SELENOPHENFURIN, AN INOSINE 5'-MONOPHOSPHATE DEHYDROGENASE INHIBITOR ANALOG OF SELENAZOFURIN, Journal of medicinal chemistry, 40(11), 1997, pp. 1731-1737
DIHYDRO(ALKYLTHIO)(NAPHTHYLMETHYL)OXOPYRIMIDINES - NOVEL NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS OF THE S-DABO SERIES
Authors: MAI A ARTICO M SBARDELLA G QUARTARONE S MASSA S LOI AG DEMONTIS A SCINTU F PUTZOLU M LACOLLA P
Citation: A. Mai et al., DIHYDRO(ALKYLTHIO)(NAPHTHYLMETHYL)OXOPYRIMIDINES - NOVEL NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS OF THE S-DABO SERIES, Journal of medicinal chemistry, 40(10), 1997, pp. 1447-1454
PYRAZOLE-RELATED NUCLEOSIDES - DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL -IODO-1-BETA-D-RIBOFURANOSYLPYRAZOLE-3-CARBOXYLATE (IPCAR), AND DERIVATIVES, AGAINST HUMAN LEUKEMIAS, LYMPHOMAS AND SOLID TUMORS CELL-LINES IN-VITRO
Authors: MANFREDINI S BAZZANINI R BARALDI PG SIMONI D VERTUANI S PANI A PINNA E SCINTU F DEMONTIS A LACOLLA P
Citation: S. Manfredini et al., PYRAZOLE-RELATED NUCLEOSIDES - DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL -IODO-1-BETA-D-RIBOFURANOSYLPYRAZOLE-3-CARBOXYLATE (IPCAR), AND DERIVATIVES, AGAINST HUMAN LEUKEMIAS, LYMPHOMAS AND SOLID TUMORS CELL-LINES IN-VITRO, Medicinal chemistry research, 6(5), 1996, pp. 293-311
METHYL-2-THIENYLKETOPOLYMETHYLENEOXYPHENYL DERIVATIVES OF ALKYL-SUBSTITUTED 4,5-DIHYDRO-OXAZOLES WITH ANTI-HUMAN PICORNAVIRUS ACTIVITY
Authors: MAI A ARTICO M MASSA S RAGNO R DEMONTIS A CORRIAS S SPIGA MG LACOLLA P
Citation: A. Mai et al., METHYL-2-THIENYLKETOPOLYMETHYLENEOXYPHENYL DERIVATIVES OF ALKYL-SUBSTITUTED 4,5-DIHYDRO-OXAZOLES WITH ANTI-HUMAN PICORNAVIRUS ACTIVITY, Antiviral chemistry & chemotherapy, 7(4), 1996, pp. 213-220
LBENZYL)-2-(2-METHYLPROPYL)THIO-4(3H)-PYRIMIDINONE (DABO-622)
Authors: ETTORRE A MAI A ARTICO M MASSA S DEMONTIS A LACOLLA P
Citation: A. Ettorre et al., LBENZYL)-2-(2-METHYLPROPYL)THIO-4(3H)-PYRIMIDINONE (DABO-622), Acta crystallographica. Section C, Crystal structure communications, 52, 1996, pp. 2115-2117
SYNTHESIS AND ANTIRHINOVIRUS ACTIVITY OF 3-(DIETHYLAMINO)-5-PHENYLISOXAZOLE DERIVATIVES
Authors: MAZZEI M GARZOGLIO R BALBI A GRANDI T DEMONTIS A CORRIAS S LACOLLA P
Citation: M. Mazzei et al., SYNTHESIS AND ANTIRHINOVIRUS ACTIVITY OF 3-(DIETHYLAMINO)-5-PHENYLISOXAZOLE DERIVATIVES, Il Farmaco, 51(5), 1996, pp. 351-359
ACYCLIC NUCLEOTIDES RELATED TO CLITOCINE - SYNTHESIS AND ANTI-HIV ACTIVITY
Authors: FRANCHETTI P CAPPELLACCI L SHEIKHA GA GRIFANTINI M LOI AG DEMONTIS A SPIGA MG LACOLLA P
Citation: P. Franchetti et al., ACYCLIC NUCLEOTIDES RELATED TO CLITOCINE - SYNTHESIS AND ANTI-HIV ACTIVITY, Nucleosides & nucleotides, 14(3-5), 1995, pp. 607-610
[[[(THIENYLCARBONYL)ALKYL]OXY]PHENYL] AND [[[(PYRRYLCARBONYL)ALKYL]OXY]PHENYL]OXAZOLINE DERIVATIVES WITH POTENT AND SELECTIVE ANTIHUMAN RHINOVIRUS ACTIVITY
Authors: MASSA S CORELLI F ARTICO M MAI A RAGNO R DEMONTIS A LOI AG CORRIAS S MARONGIU ME LACOLLA P
Citation: S. Massa et al., [[[(THIENYLCARBONYL)ALKYL]OXY]PHENYL] AND [[[(PYRRYLCARBONYL)ALKYL]OXY]PHENYL]OXAZOLINE DERIVATIVES WITH POTENT AND SELECTIVE ANTIHUMAN RHINOVIRUS ACTIVITY, Journal of medicinal chemistry, 38(5), 1995, pp. 803-809
SYNTHESIS AND ANTIVIRAL ACTIVITY OF 8-AZA ANALOGS OF CHIRAL [2-(PHOSPHONOMETHOXY)PROPYL]GUANINES
Authors: FRANCHETTI P ABUSHEIKHA G CAPPELLACCI L GRIFANTINI M DEMONTIS A PIRAS G LOI AG LACOLLA P
Citation: P. Franchetti et al., SYNTHESIS AND ANTIVIRAL ACTIVITY OF 8-AZA ANALOGS OF CHIRAL [2-(PHOSPHONOMETHOXY)PROPYL]GUANINES, Journal of medicinal chemistry, 38(20), 1995, pp. 4007-4013
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
8-AZA-ANALOGS OF PMEA AND PMEG - SYNTHESIS AND IN-VITRO ANTI-HIV ACTIVITY
Authors: FRANCHETTI P SHEIKHA GA CAPPELLACCI L MESSINA L GRIFANTINI M LOI AG DEMONTIS A SPIGA MG LACOLLA P
Citation: P. Franchetti et al., 8-AZA-ANALOGS OF PMEA AND PMEG - SYNTHESIS AND IN-VITRO ANTI-HIV ACTIVITY, Nucleosides & nucleotides, 13(8), 1994, pp. 1707-1719
8-AZA-1-DEAZAPURINE NUCLEOSIDES AS ANTIVIRAL AGENTS
Authors: FRANCHETTI P MESSINI L CAPPELLACCI L SHEIKHA GA GRIFANTINI M GUARRACINO P DEMONTIS A LOI AG MARONGIU ME LACOLLA P
Citation: P. Franchetti et al., 8-AZA-1-DEAZAPURINE NUCLEOSIDES AS ANTIVIRAL AGENTS, Nucleosides & nucleotides, 13(8), 1994, pp. 1739-1755
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
SYNTHESIS OF NEW 3,5-DISUBSTITUTED ISOXAZOLES WITH SPECIFIC ANTI-GROUP-B RHINOVIRUS ACTIVITY IN-VITRO
Authors: MAZZEI M BALBI A SOTTOFATTORI E GARZOGLIO R DEMONTIS A CORRIAS S LACOLLA P
Citation: M. Mazzei et al., SYNTHESIS OF NEW 3,5-DISUBSTITUTED ISOXAZOLES WITH SPECIFIC ANTI-GROUP-B RHINOVIRUS ACTIVITY IN-VITRO, European journal of medicinal chemistry, 28(9), 1993, pp. 669-674
SYNTHESIS AND EVALUATION OF THE ANTIVIRAL ACTIVITY OF ACYCLIC NUCLEOSIDES CARRYING FLUORINE AND SULFUR SUBSTITUENTS
Authors: BRAVO P RESNATI G VIANI F DEMONTIS A CORRIAS S LACOLLA P
Citation: P. Bravo et al., SYNTHESIS AND EVALUATION OF THE ANTIVIRAL ACTIVITY OF ACYCLIC NUCLEOSIDES CARRYING FLUORINE AND SULFUR SUBSTITUENTS, Il Farmaco, 48(8), 1993, pp. 1113-1120
Risultati: 1-22 |