| Titolo |
Pubblicato in |
Anno |
| New pyridine derivatives as inhibitors of acetylcholinesterase and amyloid aggregation |
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY |
2017 |
| New indole derivatives against C. albicans biofilm |
ESOC |
2017 |
| In vitro screening of 2-(1H-imidazol-1-yl)-1-phenylethanol derivatives as antiprotozoal agents and docking studies on Trypanosoma cruzi CYP51 |
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY |
2016 |
| Discovery of in vitro antitubercular agents through in silico ligand-based approaches |
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY |
2016 |
| Diaryl disulfides as novel stabilizers of tumor suppressor Pdcd4 |
PLOS ONE |
2016 |
| New N,N-dimethylcarbamate inhibitors of acetylcholinesterase: design synthesis and biological evaluation |
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY |
2016 |
| Exploring the anti-biofilm activity of cinnamic acid derivatives in Candida albicans |
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS |
2016 |
| Efficient synthesis of 3,5-dicarbamoyl-1,4-dihydropyridines from pyridinium salts. Key molecules in understanding NAD(P)+/NAD(P)H pathways |
JOURNAL OF HETEROCYCLIC CHEMISTRY |
2015 |
| Design, synthesis and evaluation of 3,4-dihydroxybenzoic acid derivatives as antioxidants, bio-metal chelating agents and acetylcholinesterase inhibitors |
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY |
2015 |
| (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies |
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY |
2015 |
| N‑substituted quinolinonyl diketo acid derivatives as HIV integrase strand transfer inhibitors and their activity against RNase H function of reverse transcriptase |
JOURNAL OF MEDICINAL CHEMISTRY |
2015 |
| Discovery of N-aryl-naphthylamines as in vitro inhibitors of the interaction between HIV integrase and the cofactor LEDGF/p75 |
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY |
2015 |
| Structure−activity relationship of pyrrolyl diketo acid derivatives as dual Inhibitors of HIV‑1 integrase and reverse transcriptase ribonuclease H domain |
JOURNAL OF MEDICINAL CHEMISTRY |
2015 |
