Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1396891 | European Journal of Medicinal Chemistry | 2008 | 7 Pages |
Abstract
The synthesis of indolin-2-one derivatives substituted in the 3-position by an aminomethylene group bearing either an ornithine or a lysine residue is described. The inhibitory activities of these compounds toward a panel of eight kinases were examined. Furthermore, the antibacterial activities of the prepared compounds were tested against two Gram-positive bacteria Bacillus cereus and Streptomyces chartreusis, a Gram-negative bacterium Escherichia coli and a yeast Candida albicans.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Fadoua Bouchikhi, Emilie Rossignol, Martine Sancelme, Bettina Aboab, Fabrice Anizon, Doriano Fabbro, Michelle Prudhomme, Pascale Moreau,