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Giorgio Tarzia

University of Urbino

254

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N-acylethanolamine Acid Amidase (NAAA): Structure, Functions and Inhibition.

2020 Journal of Medicinal Chemistry
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Pharmacokinetics, pharmacodynamics and safety studies on URB937, a peripherally restricted fatty acid amide hydrolase inhibitor, in rats

2019 Journal of Pharmacy and Pharmacology
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PT628. First in class melatonin MT2 receptors agonists for neuropathic pain

2016 The International Journal of Neuropsychopharmacology
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Selective melatonin MT2 receptor ligands relieve neuropathic pain through modulation of brainstem descending antinociceptive pathways.

2015 Pain
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A Potent Systemically Active N-Acylethanolamine Acid Amidase Inhibitor that Suppresses Inflammation and Human Macrophage Activation

2015 ACS Chemical Biology
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Potent, Metabolically Stable 2‐Alkyl‐8‐(2H‐1,2,3‐triazol‐2‐yl)‐9H‐adenines as Adenosine A2A Receptor Ligands

2015 ChemMedChem
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The organic chemistry of drug design and drug action

2015
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Structural determinants of peripheral O-arylcarbamate FAAH inhibitors render them dual substrates for Abcb1 and Abcg2 and restrict their access to the brain.

2014 Pharmacological Research
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Towards the development of 5-HT7 ligands combining serotonin-like and arylpiperazine moieties

2014 European Journal of Medicinal Chemistry
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Melatonin, selective and non-selective MT1/MT2 receptors agonists: Differential effects on the 24-h vigilance states

2014 Neuroscience Letters
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Citations (17)