Gilberto Spadoni

Affiliations: 
Biomolecular Sciences University of Urbino 
Area:
Organic and Medicinal Chemistry
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Publications

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Mari M, Elisi GM, Bedini A, et al. (2022) 2-Arylmelatonin analogues: Probing the 2-phenyl binding pocket of melatonin MT and MT receptors. European Journal of Medicinal Chemistry. 243: 114762
Ferlenghi F, Mari M, Gobbi G, et al. (2021) N-(anilinoethyl)amide melatonergic ligands with improved water solubility and metabolic stability. Chemmedchem
Pala D, Scalvini L, Elisi GM, et al. (2020) New classes of potent heparanase inhibitors from ligand-based virtual screening. Journal of Enzyme Inhibition and Medicinal Chemistry. 35: 1685-1696
Elisi GM, Bedini A, Scalvini L, et al. (2020) Chiral Recognition of Flexible Melatonin Receptor Ligands Induced by Conformational Equilibria. Molecules (Basel, Switzerland). 25
Piomelli D, Scalvini L, Fotio Y, et al. (2020) N-acylethanolamine Acid Amidase (NAAA): Structure, Functions and Inhibition. Journal of Medicinal Chemistry
López-Canul M, Min SH, Posa L, et al. (2019) Melatonin MT and MT Receptors Exhibit Distinct Effects in the Modulation of Body Temperature across the Light/Dark Cycle. International Journal of Molecular Sciences. 20
Olivieri D, Tarroni R, Della Ca' N, et al. (2019) Front Cover Picture: Bis‐Alkoxycarbonylation of Acrylic Esters and Amides for the Synthesis of 2‐Alkoxycarbonyl or 2‐Carbamoyl Succinates (Adv. Synth. Catal. 3/2020) Advanced Synthesis & Catalysis. 362: 437-437
Olivieri D, Tarroni R, Della Ca' N, et al. (2019) Bis‐Alkoxycarbonylation of Acrylic Esters and Amides for the Synthesis of 2‐Alkoxycarbonyl or 2‐Carbamoyl Succinates Advanced Synthesis & Catalysis. 362: 533-544
Bedini A, Fraternale A, Crinelli R, et al. (2018) Design, synthesis and biological activity of hydrogen peroxide responsive arylboronate melatonin hybrids. Chemical Research in Toxicology
Spadoni G, Bedini A, Furiassi L, et al. (2018) Identification of bivalent ligands with melatonin receptor agonist and fatty acid amide hydrolase (FAAH) inhibitory activity that exhibit ocular hypotensive effect in the rabbit. Journal of Medicinal Chemistry
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