Gilberto Spadoni

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

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Bedini A, Boutin JA, Legros C, et al. (2024) Industrial and academic approaches to the search for alternative melatonin receptor ligands: An historical survey. Journal of Pineal Research. 76: e12953
Bedini A, Elisi GM, Fanini F, et al. (2024) Binding and unbinding of potent melatonin receptor ligands: Mechanistic simulations and experimental evidence. Journal of Pineal Research. 76: e12941
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
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