Michele Mari

Affiliations: 
Biomolecular Sciences University of Urbino 
Area:
Organic and Medicinal Chemistry
Google:
"https://scholar.google.it/citations?user=x-zUbsIAAAAJ&hl=it&authuser=1"
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Publications

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Varone E, Retini M, Cherubini A, et al. (2025) Small molecule-mediated inhibition of the oxidoreductase ERO1A restrains aggressive breast cancer by impairing VEGF and PD-L1 in the tumor microenvironment. Cell Death & Disease. 16: 105
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
Bartoccini F, Mari M, Retini M, et al. (2020) Single‐Step Synthesis of Dehydroalanine Derivatives via a Brønsted Acid‐Catalyzed Multicomponent Reaction Chemistryselect. 5: 3330-3336
Retini M, Bartolucci S, Bartoccini F, et al. (2019) Concise and Convergent Enantioselective Total Syntheses of (+)- and (-)-Fumimycin. The Journal of Organic Chemistry
Bartoccini F, Venturi S, Retini M, et al. (2019) Total Synthesis of (-)-Clavicipitic Acid via γ,γ-Dimethylallyltryptophan (DMAT) and Chemoselective C-H Hydroxylation. The Journal of Organic Chemistry
Bartoccini F, Mari M, Retini M, et al. (2019) Large-Scale Preparation of N-Butanoyl-l-glutathione (C4-GSH) Organic Process Research & Development. 23: 2069-2073
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
Bartoccini F, Mari M, Retini M, et al. (2018) Organocatalytic Aza-Friedel-Crafts/Lactonization Domino Reaction of Naphthols and Phenols with 2-Acetamidoacrylate to Naphtho- and Benzofuranones Bearing a Quaternary Center at the C3 Position. The Journal of Organic Chemistry
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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