14 articles for S Di Micco
The following articles (labelled with PubMed ID or TBD) are for your review
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2,3-Dihydrobenzofuran privileged structures as new bioinspired lead compounds for the design of mPGES-1 inhibitors.

University of Salerno
Direct interaction of garcinol and related polyisoprenylated benzophenones of Garcinia cambogia fruits with the transcription factor STAT-1 as a likely mechanism of their inhibitory effect on cytokine signaling pathways.

University of Salerno
Synthesis and biological activity of cyclotetrapeptide analogues of the natural HDAC inhibitor FR235222.

University of Salerno
Novel pyrrole based CB2 agonists: New insights on CB2 receptor role in regulating neurotransmitters' tone.

University of Salerno
Design, Synthesis, and Pharmacological Characterization of a Potent Soluble Epoxide Hydrolase Inhibitor for the Treatment of Acute Pancreatitis.

University of Salerno
Rational design of the zonulin inhibitor AT1001 derivatives as potential anti SARS-CoV-2.

European Biomedical Research Institute of Salerno (Ebris)
Discovery and Optimization of Indoline-Based Compounds as Dual 5-LOX/sEH Inhibitors:

University Federico Ii of Naples
Identification of the 2-Benzoxazol-2-yl-phenol Scaffold as New Hit for JMJD3 Inhibition.

Institute of Biomolecular Chemistry (Icb)
Garcinol and Related Polyisoprenylated Benzophenones as Topoisomerase II Inhibitors: Biochemical and Molecular Modeling Studies.

European Biomedical Research Institute of Salerno (Ebris)
Identification of lead compounds as antagonists of protein Bcl-xL with a diversity-oriented multidisciplinary approach.

Universita Degli Studi Di Salerno
Synthesis, biological evaluation, and molecular docking of Ugi products containing a zinc-chelating moiety as novel inhibitors of histone deacetylases.

Universita Degli Studi Del Piemonte Orientale A. Avogadro
Discovery of new potent molecular entities able to inhibit mPGES-1.

University of Salerno
Identification by Inverse Virtual Screening of magnolol-based scaffold as new tankyrase-2 inhibitors.

University of Salerno
Discovery of new erbB4 inhibitors: Repositioning an orphan chemical library by inverse virtual screening.

University of Salerno