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Chemmedchem|June 5, 2013
Inhibition of Leishmania infantum trypanothione reductase by azole-based compounds: a comparative analysis with its physiological substrate by X-ray crystallographyPaola Baiocco, Giovanna Poce, Salvatore Alfonso, et al.Bioorganic & Medicinal Chemistry|May 18, 2013
A class of pyrrole derivatives endowed with analgesic/anti-inflammatory activityClaudio Battilocchio, Giovanna Poce, Salvatore Alfonso, et al.European Journal of Medicinal Chemistry|November 8, 2012
Improving the solubility of a new class of antiinflammatory pharmacodynamic hybrids, that release nitric oxide and inhibit cycloxygenase-2 isoenzymeMariangela Biava, Claudio Battilocchio, Giovanna Poce, et al.Journal of Medicinal Chemistry|October 6, 2007
Cyclooxygenase-2 inhibitors. 1,5-diarylpyrrol-3-acetic esters with enhanced inhibitory activity toward cyclooxygenase-2 and improved cyclooxygenase-2/cyclooxygenase-1 selectivityMariangela Biava, Giulio Cesare Porretta, Giovanna Poce, et al.Plos One|February 26, 2013
Improved BM212 MmpL3 inhibitor analogue shows efficacy in acute murine model of tuberculosis infectionGiovanna Poce, Robert H Bates, Salvatore Alfonso, et al.Journal of Medicinal Chemistry|October 14, 2011
Novel analgesic/anti-inflammatory agents: diarylpyrrole acetic esters endowed with nitric oxide releasing propertiesMariangela Biava, Giulio Cesare Porretta, Giovanna Poce, et al.Antimicrobial Agents and Chemotherapy|October 26, 2011
MmpL3 is the cellular target of the antitubercular pyrrole derivative BM212Valentina La Rosa, Giovanna Poce, Julio Ortiz Canseco, et al.Pageof 2