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Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 29, 2017
Naphthoquinone amino acid derivatives, synthesis and biological activity as proteasome inhibitors
Mauro Marastoni, Claudio Trapella, Alessandra Scotti, et al.
Expert Opinion on Therapeutic Targets
|
April 16, 2008
The P2X7 receptor as a therapeutic target
Romeo Romagnoli, Pier Giovanni Baraldi, Olga Cruz-Lopez, et al.
Bioorganic Chemistry
|
May 6, 2021
Concise synthesis and biological evaluation of 2-Aryl-3-Anilinobenzo[b]thiophene derivatives as potent apoptosis-inducing agents
Romeo Romagnoli, Delia Preti, Ernest Hamel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 17, 2009
Adenosine modulates HIF-1{alpha}, VEGF, IL-8, and foam cell formation in a human model of hypoxic foam cells
Stefania Gessi, Eleonora Fogli, Valeria Sacchetto, et al.
Journal of Medicinal Chemistry
|
September 9, 2020
Biased Agonism at Nociceptin/Orphanin FQ Receptors: A Structure Activity Study on N/OFQ(1-13)-NH<sub>2</sub>
Salvatore Pacifico, Federica Ferrari, Valentina Albanese, et al.
ACS Medicinal Chemistry Letters
|
July 18, 2019
Synthesis and Biological Activity of Peptide α-Ketoamide Derivatives as Proteasome Inhibitors
Salvatore Pacifico, Valeria Ferretti, Valentina Albanese, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
March 24, 2005
New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2
Pier Giovanni Baraldi, Romeo Romagnoli, Mojgan Aghazadeh Tabrizi, et al.
European Journal of Medicinal Chemistry
|
May 17, 2003
Recent developments in the field of A2A and A3 adenosine receptor antagonists
Pier Giovanni Baraldi, Mojgan Aghazadeh Tabrizi, Andrea Bovero, et al.
Bioorganic & Medicinal Chemistry
|
December 30, 2011
Pyrrolo- and pyrazolo-[3,4-e][1,2,4]triazolo[1,5-c]pyrimidines as adenosine receptor antagonists
Pier Giovanni Baraldi, Giulia Saponaro, Mojgan Aghazadeh Tabrizi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 21, 2025
Design and synthesis of 1,4,8-triazaspiro[4.5]decan-2-one derivatives as novel mitochondrial permeability transition pore inhibitors
Valentina Albanese, Gaia Pedriali, Martina Fabbri, et al.
Page
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Search research articles
Search
Showing results (21-30 of 98) with videos related to
Sort By:
Page
of 10
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 29, 2017
Naphthoquinone amino acid derivatives, synthesis and biological activity as proteasome inhibitors
Mauro Marastoni, Claudio Trapella, Alessandra Scotti, et al.
Expert Opinion on Therapeutic Targets
|
April 16, 2008
The P2X7 receptor as a therapeutic target
Romeo Romagnoli, Pier Giovanni Baraldi, Olga Cruz-Lopez, et al.
Bioorganic Chemistry
|
May 6, 2021
Concise synthesis and biological evaluation of 2-Aryl-3-Anilinobenzo[b]thiophene derivatives as potent apoptosis-inducing agents
Romeo Romagnoli, Delia Preti, Ernest Hamel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 17, 2009
Adenosine modulates HIF-1{alpha}, VEGF, IL-8, and foam cell formation in a human model of hypoxic foam cells
Stefania Gessi, Eleonora Fogli, Valeria Sacchetto, et al.
Journal of Medicinal Chemistry
|
September 9, 2020
Biased Agonism at Nociceptin/Orphanin FQ Receptors: A Structure Activity Study on N/OFQ(1-13)-NH<sub>2</sub>
Salvatore Pacifico, Federica Ferrari, Valentina Albanese, et al.
ACS Medicinal Chemistry Letters
|
July 18, 2019
Synthesis and Biological Activity of Peptide α-Ketoamide Derivatives as Proteasome Inhibitors
Salvatore Pacifico, Valeria Ferretti, Valentina Albanese, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
March 24, 2005
New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2
Pier Giovanni Baraldi, Romeo Romagnoli, Mojgan Aghazadeh Tabrizi, et al.
European Journal of Medicinal Chemistry
|
May 17, 2003
Recent developments in the field of A2A and A3 adenosine receptor antagonists
Pier Giovanni Baraldi, Mojgan Aghazadeh Tabrizi, Andrea Bovero, et al.
Bioorganic & Medicinal Chemistry
|
December 30, 2011
Pyrrolo- and pyrazolo-[3,4-e][1,2,4]triazolo[1,5-c]pyrimidines as adenosine receptor antagonists
Pier Giovanni Baraldi, Giulia Saponaro, Mojgan Aghazadeh Tabrizi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 21, 2025
Design and synthesis of 1,4,8-triazaspiro[4.5]decan-2-one derivatives as novel mitochondrial permeability transition pore inhibitors
Valentina Albanese, Gaia Pedriali, Martina Fabbri, et al.
Page
of 10