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Journal of Medicinal Chemistry|September 1, 2006
Carbonic anhydrase inhibitors: Hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tumor-associated isoform IXGiuseppina De Simone, Rosa Maria Vitale, Anna Di Fiore, et al.Journal of Natural Products|February 26, 2024
Phytochemical Characterization and TRPA1/TRPM8 Modulation Profile of the Cannabigerol-Rich <i>Cannabis sativa</i> L. Chemotype IVErnesto Gargiulo, Aniello Schiano Moriello, Emanuele Benetti, et al.Biochimica Et Biophysica Acta. General Subjects|January 7, 2019
Identification and characterization of phytocannabinoids as novel dual PPARα/γ agonists by a computational and in vitro experimental approachEnrico D'Aniello, Tariq Fellous, Fabio Arturo Iannotti, et al.Journal of Natural Products|February 4, 2010
Rare casbane diterpenoids from the Hainan soft coral Sinularia depressaYan Li, Marianna Carbone, Rosa Maria Vitale, et al.Biochimica Et Biophysica Acta. General Subjects|March 11, 2018
Chaperone-like effect of ceftriaxone on HEWL aggregation: A spectroscopic and computational studyPaolo Ruzza, Rosa Maria Vitale, Rohanah Hussain, et al.European Journal of Medicinal Chemistry|May 14, 2014
Structure-activity relationships and molecular modelling of new 5-arylidene-4-thiazolidinone derivatives as aldose reductase inhibitors and potential anti-inflammatory agentsRosanna Maccari, Rosa Maria Vitale, Rosaria Ottanà, et al.Data in Brief|June 16, 2018
Spectroscopy data of ceftriaxone-lysozyme interaction and computational studiesPaolo Ruzza, Rosa Maria Vitale, Rohanah Hussain, et al.The Journal of Biological Chemistry|May 9, 2007
Insights into the structural basis of the GADD45beta-mediated inactivation of the JNK kinase, MKK7/JNKK2Salvatore Papa, Simona M Monti, Rosa Maria Vitale, et al.Marine Drugs|October 21, 2020
Design, Synthesis and In Vitro Experimental Validation of Novel TRPV4 Antagonists Inspired by Labdane DiterpenesSarah Mazzotta, Gabriele Carullo, Aniello Schiano Moriello, et al.Journal of Medicinal Chemistry|September 4, 2018
Elongation of the Hydrophobic Chain as a Molecular Switch: Discovery of Capsaicin Derivatives and Endogenous Lipids as Potent Transient Receptor Potential Vanilloid Channel 2 AntagonistsAniello Schiano Moriello, Silvia López Chinarro, Olalla Novo Fernández, et al.Pageof 7