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Bioorganic & Medicinal Chemistry
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October 12, 2000
Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors
R Silvestri, M Artico, G De Martino, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
5-Alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3, 4-dihydropyrimidin-4(3H)-ones: novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives
A Mai, M Artico, G Sbardella, et al.
Bioorganic & Medicinal Chemistry
|
June 1, 1996
5H-pyrrolo[1,2-b] [1,2,5]benzothiadiazepines (PBTDs): a novel class of non-nucleoside reverse transcriptase inhibitors
M Artico, R Silvestri, E Pagnozzi, et al.
Antiviral Chemistry & Chemotherapy
|
January 6, 1999
Synthesis and biological evaluation of 5H-indolo [3,2-b][1,5]benzothiazepine derivatives, designed as conformationally constrained analogues of the human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126
R Silvestri, M Artico, B Bruno, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
June 1, 1996
Synthesis and anti-HIV activity of 10,11-dihydropyrrolo [1,2-b][1,2,5]benzothiadiazepine-11-acetic acid 5,5-dioxide derivatives and related compounds
R Silvestri, M Artico, E Pagnozzi, et al.
Journal of Medicinal Chemistry
|
May 5, 2000
Structure-based design, synthesis, and biological evaluation of novel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations
M Artico, R Silvestri, E Pagnozzi, et al.
Immunogenetics
|
January 1, 1988
Polygenic control of quantitative antibody responsiveness: restrictions of the multispecific effect related to the selection antigen
O M Ibanez, D Mouton, S L Oliveira, et al.
FEMS Microbiology Immunology
|
December 1, 1989
Salmonella typhimurium infection in high and low antibody responder mice: inverse correlation between antibody responsiveness and resistance to infection
O A Sant'Anna, S Massa, D Mouton, et al.
Journal of Medicinal Chemistry
|
March 3, 1995
[[[(Thienylcarbonyl)alkyl]oxy]phenyl]- and [[[(pyrrylcarbonyl)alkyl]oxy]phenyl]oxazoline derivatives with potent and selective antihuman rhinovirus activity
S Massa, F Corelli, M Artico, et al.
Journal of Medicinal Chemistry
|
October 10, 1998
Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: synthesis, biological evaluation, and molecular modeling
M Artico, R Di Santo, R Costi, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 145) with videos related to
Sort By:
Page
of 15
Bioorganic & Medicinal Chemistry
|
October 12, 2000
Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors
R Silvestri, M Artico, G De Martino, et al.
Journal of Medicinal Chemistry
|
March 3, 1999
5-Alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3, 4-dihydropyrimidin-4(3H)-ones: novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives
A Mai, M Artico, G Sbardella, et al.
Bioorganic & Medicinal Chemistry
|
June 1, 1996
5H-pyrrolo[1,2-b] [1,2,5]benzothiadiazepines (PBTDs): a novel class of non-nucleoside reverse transcriptase inhibitors
M Artico, R Silvestri, E Pagnozzi, et al.
Antiviral Chemistry & Chemotherapy
|
January 6, 1999
Synthesis and biological evaluation of 5H-indolo [3,2-b][1,5]benzothiazepine derivatives, designed as conformationally constrained analogues of the human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126
R Silvestri, M Artico, B Bruno, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
June 1, 1996
Synthesis and anti-HIV activity of 10,11-dihydropyrrolo [1,2-b][1,2,5]benzothiadiazepine-11-acetic acid 5,5-dioxide derivatives and related compounds
R Silvestri, M Artico, E Pagnozzi, et al.
Journal of Medicinal Chemistry
|
May 5, 2000
Structure-based design, synthesis, and biological evaluation of novel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations
M Artico, R Silvestri, E Pagnozzi, et al.
Immunogenetics
|
January 1, 1988
Polygenic control of quantitative antibody responsiveness: restrictions of the multispecific effect related to the selection antigen
O M Ibanez, D Mouton, S L Oliveira, et al.
FEMS Microbiology Immunology
|
December 1, 1989
Salmonella typhimurium infection in high and low antibody responder mice: inverse correlation between antibody responsiveness and resistance to infection
O A Sant'Anna, S Massa, D Mouton, et al.
Journal of Medicinal Chemistry
|
March 3, 1995
[[[(Thienylcarbonyl)alkyl]oxy]phenyl]- and [[[(pyrrylcarbonyl)alkyl]oxy]phenyl]oxazoline derivatives with potent and selective antihuman rhinovirus activity
S Massa, F Corelli, M Artico, et al.
Journal of Medicinal Chemistry
|
October 10, 1998
Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: synthesis, biological evaluation, and molecular modeling
M Artico, R Di Santo, R Costi, et al.
Page
of 15