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Antiviral Chemistry & Chemotherapy
|
May 20, 2000
Structure-activity relationship studies on potential non-nucleoside DABO-like inhibitors of HIV-1 reverse transcriptase
R Costi, R Di Santo, M Artico, et al.
Journal of Medicinal Chemistry
|
June 8, 2000
Synthesis, molecular modeling, and opioid receptor affinity of 9, 10-diazatricyclo[4.2.1.1(2,5)]decanes and 2,7-diazatricyclo[4.4.0. 0(3,8)]decanes structurally related to 3,8-diazabicyclo[3.2. 1]octanes
P Vianello, A Albinati, G A Pinna, et al.
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
|
December 1, 2001
[1,2,4]Triazino[4,3-a]benzimidazole acetic acid derivatives: a new class of selective aldose reductase inhibitors
F Da Settimo, G Primofiore, A Da Settimo, et al.
Journal of Medicinal Chemistry
|
July 21, 2001
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: a new class of selective A1 adenosine receptor antagonists
F Da Settimo, G Primofiore, S Taliani, et al.
Journal of Medicinal Chemistry
|
June 29, 2001
Novel N-(arylalkyl)indol-3-ylglyoxylylamides targeted as ligands of the benzodiazepine receptor: synthesis, biological evaluation, and molecular modeling analysis of the structure-activity relationships
G Primofiore, F D Settimo, S Taliani, et al.
Journal of Neuroscience Research
|
January 13, 2015
Inhibition of anandamide hydrolysis enhances noradrenergic and GABAergic transmission in the prefrontal cortex and basolateral amygdala of rats subjected to acute swim stress
Gaurav Bedse, Adele Romano, Bianca Tempesta, et al.
Journal of Medicinal Chemistry
|
November 23, 2012
New 2-(aryloxy)-3-phenylpropanoic acids as peroxisome proliferator-activated receptor α/γ dual agonists able to upregulate mitochondrial carnitine shuttle system gene expression
A Laghezza, G Pochetti, A Lavecchia, et al.
Journal of Medicinal Chemistry
|
July 27, 2001
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
A Mai, G Sbardella, M Artico, et al.
Journal of Medicinal Chemistry
|
November 16, 2011
Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity
L Porcelli, F Gilardi, A Laghezza, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Antiviral Chemistry & Chemotherapy
|
May 20, 2000
Structure-activity relationship studies on potential non-nucleoside DABO-like inhibitors of HIV-1 reverse transcriptase
R Costi, R Di Santo, M Artico, et al.
Journal of Medicinal Chemistry
|
June 8, 2000
Synthesis, molecular modeling, and opioid receptor affinity of 9, 10-diazatricyclo[4.2.1.1(2,5)]decanes and 2,7-diazatricyclo[4.4.0. 0(3,8)]decanes structurally related to 3,8-diazabicyclo[3.2. 1]octanes
P Vianello, A Albinati, G A Pinna, et al.
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
|
December 1, 2001
[1,2,4]Triazino[4,3-a]benzimidazole acetic acid derivatives: a new class of selective aldose reductase inhibitors
F Da Settimo, G Primofiore, A Da Settimo, et al.
Journal of Medicinal Chemistry
|
July 21, 2001
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: a new class of selective A1 adenosine receptor antagonists
F Da Settimo, G Primofiore, S Taliani, et al.
Journal of Medicinal Chemistry
|
June 29, 2001
Novel N-(arylalkyl)indol-3-ylglyoxylylamides targeted as ligands of the benzodiazepine receptor: synthesis, biological evaluation, and molecular modeling analysis of the structure-activity relationships
G Primofiore, F D Settimo, S Taliani, et al.
Journal of Neuroscience Research
|
January 13, 2015
Inhibition of anandamide hydrolysis enhances noradrenergic and GABAergic transmission in the prefrontal cortex and basolateral amygdala of rats subjected to acute swim stress
Gaurav Bedse, Adele Romano, Bianca Tempesta, et al.
Journal of Medicinal Chemistry
|
November 23, 2012
New 2-(aryloxy)-3-phenylpropanoic acids as peroxisome proliferator-activated receptor α/γ dual agonists able to upregulate mitochondrial carnitine shuttle system gene expression
A Laghezza, G Pochetti, A Lavecchia, et al.
Journal of Medicinal Chemistry
|
July 27, 2001
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
A Mai, G Sbardella, M Artico, et al.
Journal of Medicinal Chemistry
|
November 16, 2011
Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity
L Porcelli, F Gilardi, A Laghezza, et al.
Page
of 2