EB
Emanuela BERRINO
University of Florence, University of Naples Federico II
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Enzyme function and inhibition · Synthesis and biological activity · Cholinesterase and Neurodegenerative Diseases
0000-0002-4258-0678
Employment
Employment history is unavailable.
Education
- 2016 - 2020
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University of Naples Federico II Chimica e Tecnologia Farmaceutiche (CTF)2010 - 2015
Projects & Funding
Projects & funding information is unavailable.
Publications (55)
- First-in-class nonsteroidal anti-inflammatory drug and carbonic anhydrase inhibitor hybrid compounds as effective antimycobacterial agents Save
- Novel Insights on Benzo[b]thiophene Analogues for MAO-B Inhibition and Neuroprotection: Design, Synthesis, Molecular Modelling Studies and Biological Activity Save
- In Vitro CO-Releasing and Antioxidant Properties of Sulfonamide-Based CAI-CORMs in a H2O2-Stimulated Human Achilles Tendon-Derived Cell Model Save
- Design, synthesis, molecular modelling investigation and biological studies of novel human carbonic anhydrase inhibitors based on coumalic acid Save
- Glycosylium Ions in Superacid Mimic the Transition State of Enzyme Reactions Save
- Carbon Monoxide Release from Aryl-Propargyl Dicobalt(0)Hexacarbonyl Derivatives: A Computational and Experimental Study Save
- Accumulation, Characterization and Reactivity of Chiral Ammonium‐Carboxonium Dications in Superacid Save
- Accumulation, Characterization and Reactivity of Chiral Ammonium‐Carboxonium Dications in Superacid Save
- Carbon Monoxide Release from Aryl-Propargyl Dicobalt(0)Hexacarbonyl Derivatives: A Computational and Experimental Study Save
- A Multitarget Approach against Neuroinflammation: Alkyl Substituted Coumarins as Inhibitors of Enzymes Involved in Neurodegeneration Save
- Uncovering Novel Capsaicin Inhibitory Activity towards Human Carbonic Anhydrase Isoforms IX and XII by Combining In Silico and In Vitro Studies Save
- Angiotensin-converting enzyme Save
- Novel Insights on CAI–CORM hybrids. Evaluation of the CO releasing properties and pain-relieving activity of differently substituted coumarins for the treatment of rheumatoid arthritis Save
- New 1H‐indole‐2,3‐dione 3‐thiosemicarbazones with 3‐sulfamoylphenyl moiety as selective carbonic anhydrase inhibitors Save
- Novel Insights on Human Carbonic Anhydrase Inhibitors Based on Coumalic Acid: Design, Synthesis, Molecular Modeling Investigation, and Biological Studies Save
- New 1 H ‐indole‐2,3‐dione 3‐thiosemicarbazones with 3‐sulfamoylphenyl moiety as selective carbonic anhydrase inhibitors Save
- Modulating the Efficacy of Carbonic Anhydrase Inhibitors through Fluorine Substitution Save
- Modulating the Efficacy of Carbonic Anhydrase Inhibitors through Fluorine Substitution Save
- Dual Carbonic Anhydrase IX/XII Inhibitors and Carbon Monoxide Releasing Molecules Modulate LPS-Mediated Inflammation in Mouse Macrophages Save
- A novel class of dual-acting DCH-CORMs counteracts oxidative stress-induced inflammation in human primary tenocytes Save