Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides
โ Scribed by Franco Chimenti; Bruna Bizzarri; Adriana Bolasco; Daniela Secci; Paola Chimenti; Arianna Granese; Simone Carradori; Daniela Rivanera; Alessandra Zicari; M. Maddalena Scaltrito; Francesca Sisto
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 270 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-894X
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โฆ Synopsis
a b s t r a c t 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.
๐ SIMILAR VOLUMES
Synthesis and Photobiological Activity of N-Substituted 2-Oxo-2H-1benzopyran-3-(thio)carboxamides. -Piperidine-catalyzed condensation of benzaldehydes (I) with the malonic derivatives (II) gives a variety of polyfunctional coumarins ( III) (12 examples). They react readily with methyl iodide to the