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Analytical Chemistry|February 15, 2003
Enantioselective hydrolysis of some 2-aryloxyalkanoic acid methyl esters and isosteric analogues using a penicillin G acylase-based HPLC monolithic silica columnGabriella Massolini, Enrica Calleri, Antonio Lavecchia, et al.Biomolecules|May 16, 2023
Biological Screening and Crystallographic Studies of Hydroxy γ-Lactone Derivatives to Investigate PPARγ Phosphorylation InhibitionDavide Capelli, Giulia Cazzaniga, Matteo Mori, et al.Journal of Chemical Information and Modeling|June 9, 2016
An Effective Virtual Screening Protocol To Identify Promising p53-MDM2 InhibitorsPaolo Tortorella, Antonio Laghezza, Milena Durante, et al.Molecules (Basel, Switzerland)|July 28, 2022
Food Industry Byproducts as Starting Material for Innovative, Green Feed Formulation: A Sustainable Alternative for Poultry FeedingLeonardo Brunetti, Rosalba Leuci, Maria Antonietta Colonna, et al.European Journal of Medicinal Chemistry|November 15, 2012
Design, synthesis and biological evaluation of 5-hydroxy, 5-substituted-pyrimidine-2,4,6-triones as potent inhibitors of gelatinases MMP-2 and MMP-9Orazio Nicolotti, Marco Catto, Ilenia Giangreco, et al.Journal of the American Society of Nephrology : JASN|December 25, 2003
Investigations of pharmacologic properties of the renal CLC-K1 chloride channel co-expressed with barttin by the use of 2-(p-Chlorophenoxy)propionic acid derivatives and other structurally unrelated chloride channels blockersAntonella Liantonio, Michael Pusch, Alessandra Picollo, et al.Proceedings of the National Academy of Sciences of the United States of America|January 25, 2008
Molecular switch for CLC-K Cl- channel block/activation: optimal pharmacophoric requirements towards high-affinity ligandsAntonella Liantonio, Alessandra Picollo, Giuseppe Carbonara, et al.Acta Crystallographica. Section D, Biological Crystallography|July 10, 2014
Structural basis of the transactivation deficiency of the human PPARγ F360L mutant associated with familial partial lipodystrophyClorinda Lori, Alessandra Pasquo, Roberta Montanari, et al.Journal of Medicinal Chemistry|September 11, 2018
Identification of the First PPARα/γ Dual Agonist Able To Bind to Canonical and Alternative Sites of PPARγ and To Inhibit Its Cdk5-Mediated PhosphorylationAntonio Laghezza, Luca Piemontese, Carmen Cerchia, et al.European Journal of Medicinal Chemistry|December 13, 2021
Development of novel phenoxyalkylpiperidines as high-affinity Sigma-1 (σ1) receptor ligands with potent anti-amnesic effectFrancesca S Abatematteo, Philip D Mosier, Mauro Niso, et al.Pageof 9