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European Journal of Medicinal Chemistry
|
September 23, 2022
2-Arylmelatonin analogues: Probing the 2-phenyl binding pocket of melatonin MT<sub>1</sub> and MT<sub>2</sub> receptors
Michele Mari, Gian Marco Elisi, Annalida Bedini, et al.
Pharmaceuticals (Basel, Switzerland)
|
April 23, 2022
4-Heteroaryl Substituted Amino-3,5-Dicyanopyridines as New Adenosine Receptor Ligands: Novel Insights on Structure-Activity Relationships and Perspectives
Daniela Catarzi, Flavia Varano, Erica Vigiani, et al.
Journal of Medicinal Chemistry
|
October 16, 2004
Synthesis and biological evaluation of novel N6-[4-(substituted)sulfonamidophenylcarbamoyl]adenosine-5'-uronamides as A3 adenosine receptor agonists
Pier Giovanni Baraldi, Francesca Fruttarolo, Mojgan Aghazadeh Tabrizi, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 14, 2020
Structural investigation on thiazolo[5,4-d]pyrimidines to obtain dual-acting blockers of CD73 and adenosine A<sub>2A</sub> receptor as potential antitumor agents
Flavia Varano, Daniela Catarzi, Fabrizio Vincenzi, et al.
Journal of Medicinal Chemistry
|
August 9, 2002
Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist
Anna Maconi, Giorgia Pastorin, Tatiana Da Ros, et al.
Journal of Medicinal Chemistry
|
January 19, 2007
Synthesis and biological evaluation of novel 1-deoxy-1-[6-[((hetero)arylcarbonyl)hydrazino]- 9H-purin-9-yl]-N-ethyl-beta-D-ribofuranuronamide derivatives as useful templates for the development of A2B adenosine receptor agonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Chemmedchem
|
October 4, 2022
Synthesis of Unsymmetrical Squaramides as Allosteric GSK-3β Inhibitors Promoting β-Catenin-Mediated Transcription of TCF/LEF in Retinal Pigment Epithelial Cells
Gabriele Carullo, Laura Bottoni, Silvia Pasquini, et al.
Psychopharmacology
|
May 26, 2023
MAM-2201 acute administration impairs motor, sensorimotor, prepulse inhibition, and memory functions in mice: a comparison with its analogue AM-2201
Giorgia Corli, Micaela Tirri, Sabrine Bilel, et al.
Journal of Medicinal Chemistry
|
June 29, 2012
7-Oxo-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxamides as selective CB(2) cannabinoid receptor ligands: structural investigations around a novel class of full agonists
Pier Giovanni Baraldi, Giulia Saponaro, Allan R Moorman, et al.
Molecular Pharmacology
|
March 25, 2005
Expression, pharmacological profile, and functional coupling of A2B receptors in a recombinant system and in peripheral blood cells using a novel selective antagonist radioligand, [3H]MRE 2029-F20
Stefania Gessi, Katia Varani, Stefania Merighi, et al.
Page
of 24
Search research articles
Search
Showing results (181-190 of 239) with videos related to
Sort By:
Page
of 24
European Journal of Medicinal Chemistry
|
September 23, 2022
2-Arylmelatonin analogues: Probing the 2-phenyl binding pocket of melatonin MT<sub>1</sub> and MT<sub>2</sub> receptors
Michele Mari, Gian Marco Elisi, Annalida Bedini, et al.
Pharmaceuticals (Basel, Switzerland)
|
April 23, 2022
4-Heteroaryl Substituted Amino-3,5-Dicyanopyridines as New Adenosine Receptor Ligands: Novel Insights on Structure-Activity Relationships and Perspectives
Daniela Catarzi, Flavia Varano, Erica Vigiani, et al.
Journal of Medicinal Chemistry
|
October 16, 2004
Synthesis and biological evaluation of novel N6-[4-(substituted)sulfonamidophenylcarbamoyl]adenosine-5'-uronamides as A3 adenosine receptor agonists
Pier Giovanni Baraldi, Francesca Fruttarolo, Mojgan Aghazadeh Tabrizi, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 14, 2020
Structural investigation on thiazolo[5,4-d]pyrimidines to obtain dual-acting blockers of CD73 and adenosine A<sub>2A</sub> receptor as potential antitumor agents
Flavia Varano, Daniela Catarzi, Fabrizio Vincenzi, et al.
Journal of Medicinal Chemistry
|
August 9, 2002
Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist
Anna Maconi, Giorgia Pastorin, Tatiana Da Ros, et al.
Journal of Medicinal Chemistry
|
January 19, 2007
Synthesis and biological evaluation of novel 1-deoxy-1-[6-[((hetero)arylcarbonyl)hydrazino]- 9H-purin-9-yl]-N-ethyl-beta-D-ribofuranuronamide derivatives as useful templates for the development of A2B adenosine receptor agonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Chemmedchem
|
October 4, 2022
Synthesis of Unsymmetrical Squaramides as Allosteric GSK-3β Inhibitors Promoting β-Catenin-Mediated Transcription of TCF/LEF in Retinal Pigment Epithelial Cells
Gabriele Carullo, Laura Bottoni, Silvia Pasquini, et al.
Psychopharmacology
|
May 26, 2023
MAM-2201 acute administration impairs motor, sensorimotor, prepulse inhibition, and memory functions in mice: a comparison with its analogue AM-2201
Giorgia Corli, Micaela Tirri, Sabrine Bilel, et al.
Journal of Medicinal Chemistry
|
June 29, 2012
7-Oxo-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxamides as selective CB(2) cannabinoid receptor ligands: structural investigations around a novel class of full agonists
Pier Giovanni Baraldi, Giulia Saponaro, Allan R Moorman, et al.
Molecular Pharmacology
|
March 25, 2005
Expression, pharmacological profile, and functional coupling of A2B receptors in a recombinant system and in peripheral blood cells using a novel selective antagonist radioligand, [3H]MRE 2029-F20
Stefania Gessi, Katia Varani, Stefania Merighi, et al.
Page
of 24