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Nature Communications|October 10, 2023
Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2Sarath Ramachandran, Nikolai Makukhin, Kevin Haubrich, et al.
Bioorganic & Medicinal Chemistry|September 3, 2008
Improvement of water solubility of non-competitive AMPA receptor antagonists by complexation with beta-cyclodextrinRosanna Stancanelli, Vincenza Crupi, Laura De Luca, et al.
European Journal of Medicinal Chemistry|November 5, 2016
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitorsStefania Ferro, Laura De Luca, Maria Paola Germanò, et al.
Chemmedchem|February 27, 2016
In Vivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant AgentsElvira Bruno, Maria R Buemi, Laura De Luca, et al.
RSC Medicinal Chemistry|June 25, 2025
Structure-based design and evaluation of tyrosinase inhibitors targeting both human and mushroom isozymesSalvatore Mirabile, Giovanna Pitasi, Sonia Floris, et al.
Bioorganic & Medicinal Chemistry|January 14, 2014
Synthesis, modelling and biological characterization of 3-substituted-1H-indoles as ligands of GluN2B-containing N-methyl-d-aspartate receptorsRosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Journal of Medicinal Chemistry|April 11, 2018
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine FragmentsStefania Ferro, Batel Deri, Maria Paola Germanò, et al.
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