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PNAS Nexus
|
January 30, 2023
Pharmacological potentiators of the calcium signaling cascade identified by high-throughput screening
Michele Genovese, Daniela Guidone, Martina Buccirossi, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 1, 2010
Neuropeptide FF receptors have opposing modulatory effects on nociception
Jelveh Lameh, Fabio Bertozzi, Nicholas Kelly, et al.
Journal of Medicinal Chemistry
|
November 8, 2014
Synthesis, biological evaluation, and 3D QSAR study of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters as N-acylethanolamine acid amidase (NAAA) inhibitors
Stefano Ponzano, Anna Berteotti, Rita Petracca, et al.
Chemmedchem
|
May 16, 2014
3-Aminoazetidin-2-one derivatives as N-acylethanolamine acid amidase (NAAA) inhibitors suitable for systemic administration
Annalisa Fiasella, Andrea Nuzzi, Maria Summa, et al.
Journal of Medicinal Chemistry
|
April 26, 2013
Discovery of a new class of highly potent inhibitors of acid ceramidase: synthesis and structure-activity relationship (SAR)
Daniela Pizzirani, Chiara Pagliuca, Natalia Realini, et al.
Pharmacological Research
|
August 15, 2021
Inhibition of N-acylethanolamine-hydrolyzing acid amidase reduces T cell infiltration in a mouse model of multiple sclerosis
Stefania Sgroi, Elisa Romeo, Paolo Di Fruscia, et al.
Journal of Medicinal Chemistry
|
October 7, 2009
Discovery of selective nonpeptidergic neuropeptide FF2 receptor agonists
Gilles Gaubert, Fabio Bertozzi, Nicholas M Kelly, et al.
Journal of Medicinal Chemistry
|
February 10, 2025
Target Identification with Live-Cell Photoaffinity Labeling and Mechanism of Action Elucidation of ARN23765, a Highly Potent CFTR Corrector
Elisa Romeo, Francesco Saccoliti, Riccardo Ocello, et al.
Chemmedchem
|
January 10, 2014
Synthesis, structure-activity, and structure-stability relationships of 2-substituted-N-(4-oxo-3-oxetanyl) N-acylethanolamine acid amidase (NAAA) inhibitors
Romina Vitale, Giuliana Ottonello, Rita Petracca, et al.
European Journal of Medicinal Chemistry
|
February 12, 2016
Potent α-amino-β-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure-activity relationship (SAR) studies
Andrea Nuzzi, Annalisa Fiasella, Jose Antonio Ortega, et al.
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Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
PNAS Nexus
|
January 30, 2023
Pharmacological potentiators of the calcium signaling cascade identified by high-throughput screening
Michele Genovese, Daniela Guidone, Martina Buccirossi, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 1, 2010
Neuropeptide FF receptors have opposing modulatory effects on nociception
Jelveh Lameh, Fabio Bertozzi, Nicholas Kelly, et al.
Journal of Medicinal Chemistry
|
November 8, 2014
Synthesis, biological evaluation, and 3D QSAR study of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters as N-acylethanolamine acid amidase (NAAA) inhibitors
Stefano Ponzano, Anna Berteotti, Rita Petracca, et al.
Chemmedchem
|
May 16, 2014
3-Aminoazetidin-2-one derivatives as N-acylethanolamine acid amidase (NAAA) inhibitors suitable for systemic administration
Annalisa Fiasella, Andrea Nuzzi, Maria Summa, et al.
Journal of Medicinal Chemistry
|
April 26, 2013
Discovery of a new class of highly potent inhibitors of acid ceramidase: synthesis and structure-activity relationship (SAR)
Daniela Pizzirani, Chiara Pagliuca, Natalia Realini, et al.
Pharmacological Research
|
August 15, 2021
Inhibition of N-acylethanolamine-hydrolyzing acid amidase reduces T cell infiltration in a mouse model of multiple sclerosis
Stefania Sgroi, Elisa Romeo, Paolo Di Fruscia, et al.
Journal of Medicinal Chemistry
|
October 7, 2009
Discovery of selective nonpeptidergic neuropeptide FF2 receptor agonists
Gilles Gaubert, Fabio Bertozzi, Nicholas M Kelly, et al.
Journal of Medicinal Chemistry
|
February 10, 2025
Target Identification with Live-Cell Photoaffinity Labeling and Mechanism of Action Elucidation of ARN23765, a Highly Potent CFTR Corrector
Elisa Romeo, Francesco Saccoliti, Riccardo Ocello, et al.
Chemmedchem
|
January 10, 2014
Synthesis, structure-activity, and structure-stability relationships of 2-substituted-N-(4-oxo-3-oxetanyl) N-acylethanolamine acid amidase (NAAA) inhibitors
Romina Vitale, Giuliana Ottonello, Rita Petracca, et al.
European Journal of Medicinal Chemistry
|
February 12, 2016
Potent α-amino-β-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure-activity relationship (SAR) studies
Andrea Nuzzi, Annalisa Fiasella, Jose Antonio Ortega, et al.
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of 4