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Molecules (Basel, Switzerland)|September 23, 2020
Chemoinformatic Database Building and in Silico Hit-Identification of Potential Multi-Targeting Bioactive Compounds Extracted from Mushroom SpeciesAnnalisa Maruca, Federica Moraca, Roberta Rocca, et al.European Journal of Medicinal Chemistry|June 29, 2013
Exploring 4-substituted-2-thiazolylhydrazones from 2-, 3-, and 4-acetylpyridine as selective and reversible hMAO-B inhibitorsPaola Chimenti, Anél Petzer, Simone Carradori, et al.European Journal of Medicinal Chemistry|May 27, 2024
MAATrica: a measure for assessing consistency and methods in medicinal and nutraceutical chemistry papersGiulia Panzarella, Alessandro Gallo, Sandra Coecke, et al.Bioorganic & Medicinal Chemistry Letters|June 9, 2006
Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2H-benzopyran]-3-carboxamidesFranco Chimenti, Daniela Secci, Adriana Bolasco, et al.Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|October 25, 2016
SGK1, the New Player in the Game of Resistance: Chemo-Radio Molecular Target and Strategy for InhibitionCristina Talarico, Vincenzo Dattilo, Lucia D'Antona, et al.Journal of Medicinal Chemistry|April 22, 2009
Chalcones: a valid scaffold for monoamine oxidases inhibitorsFranco Chimenti, Rossella Fioravanti, Adriana Bolasco, et al.Bioorganic & Medicinal Chemistry|April 26, 2005
Biocatalysed synthesis of beta-O-glucosides from 9-fluorenon-2-carbohydroxyesters. Part 3: IFN-inducing and anti-HSV-2 propertiesStefano Alcaro, Adriana Arena, Rosaria Di Bella, et al.Drug Resistance Updates : Reviews and Commentaries in Antimicrobial and Anticancer Chemotherapy|February 8, 2011
Molecular and structural aspects of clinically relevant mutations related to the approved non-nucleoside inhibitors of HIV-1 reverse transcriptaseStefano Alcaro, Claudia Alteri, Anna Artese, et al.Bioorganic & Medicinal Chemistry|July 10, 2010
Investigations on the 2-thiazolylhydrazyne scaffold: synthesis and molecular modeling of selective human monoamine oxidase inhibitorsFranco Chimenti, Adriana Bolasco, Daniela Secci, et al.Journal of Medicinal Chemistry|February 3, 2007
Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitorsFranco Chimenti, Rossella Fioravanti, Adriana Bolasco, et al.Pageof 13