Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides
Academic Article
Publication Date:
2010
Citation:
Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides / F. Chimenti, B. Bizzarri, A. Bolasco, D. Secchi, P. Chimenti, A. Granese, S. Carradori, D. Rivanera, A. Zicari, M.M. Scaltrito, F. Sisto. - In: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - ISSN 0960-894X. - 20:16(2010), pp. 4922-4926. [10.1016/j.bmcl.2010.06.048]
abstract:
N-substituted-3-carboxamido-coumarin derivatives were prepared and evaluated for selective antibacterial activity against 20 isolates of Helicobacter pylori clinical strains, including five metronidazole resistant ones. Some of them possessed the best activity against H. pylori metronidazole resistant strains with MIC values lower than the drug reference (metronidazole). Furthermore, anti-inflammatory activity through the inhibition of the IL-8 production was investigated.
IRIS type:
01 - Articolo su periodico
Keywords:
Antimicrobial activity; Coumarin; Cytotoxicity; Helicobacter pylori
List of contributors:
F. Chimenti, B. Bizzarri, A. Bolasco, D. Secchi, P. Chimenti, A. Granese, S. Carradori, D. Rivanera, A. Zicari, M.M. Scaltrito, F. Sisto
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