2007
DOI: 10.1007/s11094-007-0107-1
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Synthesis and antimicrobial activity of substituted amides and hydrazides of N-acyl-5-bromanthranilic acids

Abstract: A series of 17 new substituted amides and hydrazides of N-acyl-5-bromanthranilic acids were synthesized. The antimicrobial activity of these compounds with respect to St. aureus and E. coli was evaluated. It was found that of N-chloracetyl-5-bromanthranlic acid methylamide and hydrazide significantly suppressed the growth of test microbes, with a minimum inhibitory concentration of 15.6 mg/ml against St. aureus and 15.6 -31.5 mg/ml against E. coli. The other tested compounds were significantly less active. 483… Show more

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Cited by 4 publications
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“…2 Furthermore, the corresponding N-acyl anthranilic amide 16 was obtained in 87% yield via the aminolysis of benzoxazinone with tryptamine (Scheme 5). 17 In summary, we have developed a silver-catalyzed practical synthesis of valuable N-acyl anthranilic acids from readily available anthranils and carboxylic acids. This protocol is likely achieved via a Ag 2 O-catalyzed imino-ketene generation from anthranils.…”
Section: ■ Introductionmentioning
confidence: 99%
“…2 Furthermore, the corresponding N-acyl anthranilic amide 16 was obtained in 87% yield via the aminolysis of benzoxazinone with tryptamine (Scheme 5). 17 In summary, we have developed a silver-catalyzed practical synthesis of valuable N-acyl anthranilic acids from readily available anthranils and carboxylic acids. This protocol is likely achieved via a Ag 2 O-catalyzed imino-ketene generation from anthranils.…”
Section: ■ Introductionmentioning
confidence: 99%
“…В работах [3][4] разработаны QSAR модели молекулярного дизайна для производных антраниловой кислоты, учитывающих противомикробную, анальгетическую и противовоспалительную активность.…”
Section: Introductionunclassified