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Pharmaceuticals (Basel, Switzerland)|July 27, 2024
A Dynamic and Effective Peptide-Based Strategy for Promptly Addressing Emerging SARS-CoV-2 Variants of ConcernMichela Murdocca, Isabella Romeo, Gennaro Citro, et al.
Bioinformatics (Oxford, England)|January 9, 2013
Detecting and understanding genetic and structural features in HIV-1 B subtype V3 underlying HIV-1 co-receptor usageMengjie Chen, Valentina Svicher, Anna Artese, et al.
Archiv Der Pharmazie|April 21, 2025
Discover the Power of Lithospermic Acid as Human Carbonic Anhydrase VA and Pancreatic Lipase Inhibitor Through In Silico and In Vitro StudiesEmanuele Liborio Citriniti, Roberta Rocca, Giosuè Costa, et al.
Journal of Medicinal Chemistry|January 27, 2007
Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivativesFranco Chimenti, Elias Maccioni, Daniela Secci, et al.
Chemmedchem|March 24, 2016
Hit Identification of a Novel Dual Binder for h-telo/c-myc G-Quadruplex by a Combination of Pharmacophore Structure-Based Virtual Screening and Docking RefinementRoberta Rocca, Giosuè Costa, Anna Artese, et al.
Biochimica Et Biophysica Acta. General Subjects|December 28, 2016
Identification of G-quadruplex DNA/RNA binders: Structure-based virtual screening and biophysical characterizationRoberta Rocca, Federica Moraca, Giosuè Costa, et al.
ACS Medicinal Chemistry Letters|May 22, 2020
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XIIRita Meleddu, Simona Distinto, Filippo Cottiglia, et al.
European Journal of Pharmacology|July 20, 2002
Modeling and biological evaluation of 3,3'-(1,2-ethanediyl)bis[2-(4-methoxyphenyl)-thiazolidin-4-one], a new synthetic cyclooxygenase-2 inhibitorRosaria Ottaná, Emanuela Mazzon, Laura Dugo, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitorsFranco Chimenti, Rossella Fioravanti, Adriana Bolasco, et al.
Current Medicinal Chemistry|May 25, 2006
Synthesis, biological evaluation and 3D-QSAR of 1,3,5-trisubstituted-4,5-dihydro-(1H)-pyrazole derivatives as potent and highly selective monoamine oxidase A inhibitorsFranco Chimenti, Adriana Bolasco, Fedele Manna, et al.
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