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Results: 1-25 | 26-31
Results: 1-25/31
1-Amino-6-chloro-2-(1H-pyrrol-2-yl)benzimidazole (RS 1350)
Authors: Pifferi, A Camalli, M Silvestri, R De Martino, G Massa, S Artico, M
Citation: A. Pifferi et al., 1-Amino-6-chloro-2-(1H-pyrrol-2-yl)benzimidazole (RS 1350), ACT CRYST E, 57, 2001, pp. o819-o821
1-{[4-(4-chlorophenyl)-1H-pyrrol-3-yl](2,4-dichloro-phenyl)methyl}-1H-imidazole (RDS 416)
Authors: Camalli, M Pifferi, A Costi, R Di Santo, R Massa, S Artico, M
Citation: M. Camalli et al., 1-{[4-(4-chlorophenyl)-1H-pyrrol-3-yl](2,4-dichloro-phenyl)methyl}-1H-imidazole (RDS 416), ACT CRYST E, 57, 2001, pp. O96-O98
B cell development and immunoglobulin gene transcription in the absence ofOct-2 and OBF-1
Authors: Schubart, K Massa, S Schubart, D Corcoran, LM Rolink, AG Matthias, P
Citation: K. Schubart et al., B cell development and immunoglobulin gene transcription in the absence ofOct-2 and OBF-1, NAT IMMUNOL, 2(1), 2001, pp. 69-74
Crystal structure of 7-chloropyrrolo[1,2-b][1,2,5]benzothiadiazepin-10(11H)-one-5,5-dioxide, C11H7N2O3ClS
Authors: Ettorre, A Silvestri, R Artico, M Massa, S La Colla, P
Citation: A. Ettorre et al., Crystal structure of 7-chloropyrrolo[1,2-b][1,2,5]benzothiadiazepin-10(11H)-one-5,5-dioxide, C11H7N2O3ClS, Z KRIST-NEW, 216(1), 2001, pp. 57-58
Growth inhibition by glucose oxidase system of enterotoxic Escherichia coli and Salmonella derby: in vitro studies
Authors: Massa, S Petruccioli, M Brocchi, GF Altieri, C Sinigaglia, M Spano, G
Citation: S. Massa et al., Growth inhibition by glucose oxidase system of enterotoxic Escherichia coli and Salmonella derby: in vitro studies, WORLD J MIC, 17(3), 2001, pp. 287-291
Evaluation of recovery methods to detect faecal streptococci in polluted waters
Authors: Massa, S Brocchi, GF Peri, G Altieri, C Mammina, C
Citation: S. Massa et al., Evaluation of recovery methods to detect faecal streptococci in polluted waters, LETT APPL M, 32(5), 2001, pp. 298-302
Detection of anthrax vaccine virulence factors by polymerase chain reaction
Authors: Fasanella, A Losito, S Trotta, T Adone, R Massa, S Ciuchini, F Chiocco, D
Citation: A. Fasanella et al., Detection of anthrax vaccine virulence factors by polymerase chain reaction, VACCINE, 19(30), 2001, pp. 4214-4218
The occurrence of Aeromonas spp. in natural mineral water and well water
Authors: Massa, S Altieri, C D'Angela, A
Citation: S. Massa et al., The occurrence of Aeromonas spp. in natural mineral water and well water, INT J F MIC, 63(1-2), 2001, pp. 169-173
A new facile and expeditious synthesis of N-hydroxy-N '-phenyloctanediamide, a potent inducer of terminal cytodifferentiation
Authors: Mai, A Esposito, M Sbardella, G Massa, S
Citation: A. Mai et al., A new facile and expeditious synthesis of N-hydroxy-N '-phenyloctanediamide, a potent inducer of terminal cytodifferentiation, ORG PREP PR, 33(4), 2001, pp. 391-394
Structure-based design, synthesis, and biological evaluation of conformationally restricted novel 2-alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as non-nucleoside inhibitors of HIV-1 reverse transcriptase
Authors: Mai, A Sbardella, G Artico, M Ragno, R Massa, S Novellino, E Greco, G Lavecchia, A Musiu, C La Colla, M Murgioni, C La Colla, P Loddo, R
Citation: A. Mai et al., Structure-based design, synthesis, and biological evaluation of conformationally restricted novel 2-alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as non-nucleoside inhibitors of HIV-1 reverse transcriptase, J MED CHEM, 44(16), 2001, pp. 2544-2554
3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors
Authors: Massa, S Mai, A Sbardella, G Esposito, M Ragno, R Loidl, P Brosch, G
Citation: S. Massa et al., 3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors, J MED CHEM, 44(13), 2001, pp. 2069-2072
Molecular mechanisms of extinction: old findings and new ideas
Authors: Massa, S Junker, S Matthias, P
Citation: S. Massa et al., Molecular mechanisms of extinction: old findings and new ideas, INT J BIO C, 32(1), 2000, pp. 23-40
Does the 2-methylthiomethyl substituent really confer high anti-HIV-1 activity to S-DABOS?
Authors: Sbardella, G Mai, A Artico, M Massa, S Marceddu, T Vargiu, L Marongiu, ME La Colla, P
Citation: G. Sbardella et al., Does the 2-methylthiomethyl substituent really confer high anti-HIV-1 activity to S-DABOS?, MED CHEM RE, 10(1), 2000, pp. 30-39
Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors
Authors: Silvestri, R Artico, M De Martino, G Novellino, E Greco, G Lavecchia, A Massa, S Loi, AG Doratiotto, S La Colla, P
Citation: R. Silvestri et al., Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors, BIO MED CH, 8(9), 2000, pp. 2305-2309
Antimycobacterial pyrroles: Synthesis, anti-Mycobacterium tuberculosis activity and QSAR studies
Authors: Ragno, R Marshall, GR Di Santo, R Costi, R Massa, S Rompei, R Artico, M
Citation: R. Ragno et al., Antimycobacterial pyrroles: Synthesis, anti-Mycobacterium tuberculosis activity and QSAR studies, BIO MED CH, 8(6), 2000, pp. 1423-1432
1-[2-(Diphenylmethoxy)ethyl]-2-methyl-5-nitroimidazole: a potent lead for the design of novel NNRTIs
Authors: Silvestri, R Artico, M Massa, S Marceddu, T De Montis, F La Colla, P
Citation: R. Silvestri et al., 1-[2-(Diphenylmethoxy)ethyl]-2-methyl-5-nitroimidazole: a potent lead for the design of novel NNRTIs, BIOORG MED, 10(3), 2000, pp. 253-256
Structure-activity relationship studies on potential non-nucleoside DABO-like inhibitors of HIV-1 reverse transcriptase
Authors: Costi, R Di Santo, R Artico, M Massa, S Lavecchia, A Marceddu, T Sanna, L La Colla, P Marongiu, ME
Citation: R. Costi et al., Structure-activity relationship studies on potential non-nucleoside DABO-like inhibitors of HIV-1 reverse transcriptase, ANTIVIR CHE, 11(2), 2000, pp. 117-133
Chiral resolution and molecular modeling investigation of rac-2-cyclopentylthio-6[1-(2,6-difluorophenyl)ethyl]-3,4-dihydro-5-methylpyrimidin-4(3H)-one (MC-1047), a potent anti-HIV-1 reverse transcriptase agent of the DABO class
Authors: Quaglia, MG Mai, A Sbardella, G Artico, M Ragno, R Massa, S Del Piano, D Setzu, G Doratiotto, S Cotichini, V
Citation: Mg. Quaglia et al., Chiral resolution and molecular modeling investigation of rac-2-cyclopentylthio-6[1-(2,6-difluorophenyl)ethyl]-3,4-dihydro-5-methylpyrimidin-4(3H)-one (MC-1047), a potent anti-HIV-1 reverse transcriptase agent of the DABO class, CHIRALITY, 13(2), 2000, pp. 75-80
Reductive smiles rearrangement of 1-[(5-chloro-2-nitrophenyl)sulfonyl]-1H-pyrrole-2-carbohydrazide to 1-amino-6-chloro-2-(1H-pyrrol-2-yl)benzimidazole
Authors: Silvestri, R Pifferi, A De Martino, G Massa, S Saturnino, C Artico, M
Citation: R. Silvestri et al., Reductive smiles rearrangement of 1-[(5-chloro-2-nitrophenyl)sulfonyl]-1H-pyrrole-2-carbohydrazide to 1-amino-6-chloro-2-(1H-pyrrol-2-yl)benzimidazole, HETEROCYCLE, 53(10), 2000, pp. 2163
Effects of transient global ischemia and kainate on poly(ADP-ribose) polymerase (PARP) gene expression and proteolytic cleavage in gerbil and rat brains
Authors: Liu, JL Ying, WH Massa, S Duriez, PJ Swanson, RA Poirier, GG Sharp, FR
Citation: Jl. Liu et al., Effects of transient global ischemia and kainate on poly(ADP-ribose) polymerase (PARP) gene expression and proteolytic cleavage in gerbil and rat brains, MOL BRAIN R, 80(1), 2000, pp. 7-16
Structure-based design, synthesis, and biological evaluation of navel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations
Authors: Artico, M Silvestri, R Pagnozzi, E Bruno, B Novellino, E Greco, G Massa, S Ettorre, A Loi, AG Scintu, F La Colla, P
Citation: M. Artico et al., Structure-based design, synthesis, and biological evaluation of navel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations, J MED CHEM, 43(9), 2000, pp. 1886-1891
Note: Susceptibility to chlorine of Aeromonas hydrophila strains
Authors: Massa, S Armuzzi, R Tosques, M Canganella, F Trovatelli, LD
Citation: S. Massa et al., Note: Susceptibility to chlorine of Aeromonas hydrophila strains, J APPL MICR, 86(1), 1999, pp. 169-173
Pyridinylpyrrolyl analogs of isoniazid: Synthesis and antimycobacterial activities
Authors: Costi, R Artico, M Di Santo, R De Martino, G Massa, S Deidda, D Lampis, G Pompei, R
Citation: R. Costi et al., Pyridinylpyrrolyl analogs of isoniazid: Synthesis and antimycobacterial activities, MED CHEM RE, 9(6), 1999, pp. 408-423
N-[4-(1,1 '-biphenylyl)methyl]-4-(4-thiomorpholinylmethyl) benzenamines, anew class of synthetic antituberculosis agents active against Mycobacterium avium
Authors: Mai, A Sbardella, G Artico, M Massa, S Lampis, G Deidda, D Pompei, R
Citation: A. Mai et al., N-[4-(1,1 '-biphenylyl)methyl]-4-(4-thiomorpholinylmethyl) benzenamines, anew class of synthetic antituberculosis agents active against Mycobacterium avium, MED CHEM RE, 9(3), 1999, pp. 149-161
Nitroquinolones with broad-spectrum antimycobacterial activity in vitro
Authors: Artico, M Mai, A Sbardella, G Massa, S Musiu, C Lostia, S Demontis, F La Colla, P
Citation: M. Artico et al., Nitroquinolones with broad-spectrum antimycobacterial activity in vitro, BIOORG MED, 9(12), 1999, pp. 1651-1656
Risultati: 1-25 | 26-31