Rita Meleddu
Via Ospedale 72
Cagliari, 09124, Italy
Cagliari, 09124, Italy
Last Updated: 09/26/2026
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Found 35 publications
Structure-based virtual screening leads to the discovery of a 4,5-dihydropyrazole derivative as the first dual inhibitor of West Nile virus NS3 helicase and protease.
Journal: European journal of medicinal chemistry
Published: June 23, 2026
The natural coumarin 7-methoxy-8-isopentenyloxycoumarin alleviates LPS-induced inflammation by suppressing NF-κB and the MAPK/AP-1 pathways and accelerating COX-2 proteasomal degradation.
Journal: European journal of pharmacology
Published: January 23, 2026
Synthesis and Evaluation of Thiazolidinone-Isatin Hybrids for Selective Inhibition of Cancer-Related Carbonic Anhydrases.
Journal: ACS medicinal chemistry letters
Published: December 12, 2024
Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase Inhibitors.
Journal: Molecules (Basel, Switzerland)
Published: July 31, 2024
New Structural Features of Isatin Dihydrothiazole Hybrids for Selective Carbonic Anhydrase Inhibitors.
Journal: ACS medicinal chemistry letters
Published: June 15, 2024
Exploring the 1-(4-Nitrophenyl)-3-arylprop-2-en-1-one Scaffold for the Selective Inhibition of Monoamine Oxidase B.
Journal: ACS medicinal chemistry letters
Published: May 29, 2024
Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: December 07, 2023
2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: October 23, 2023
5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action.
Journal: Frontiers in cellular and infection microbiology
Published: March 24, 2023
Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase-associated RNase H function.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: March 15, 2021
Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions.
Journal: Molecules (Basel, Switzerland)
Published: February 22, 2021
Last Updated: 09/26/2026