<p>The oxofuran ring opening of 4-substituted <i>N</i>′-(5-aryl-2-oxofuran-3(2<i>H</i>)-ylidene)-benzhydrazides upon the reaction with different alkylamines gave new modified <i>N</i>-alkyl-2-aroylhydrazinylidene-4-oxobutanamides. The synthesized compounds demonstrated pronounced anti-inflammatory activity <i>in vivo</i> and proved themselves as promising drug candidates for the treatment of inflammation.</p>

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Synthesis and study of anti-inflammatory activity of N-alkyl-2-aroylhydrazinylidene-4-oxobutanamides

  • E. I. Denisova,
  • O. V. Zvereva,
  • D. V. Lipin,
  • S. V. Chashchina,
  • I. N. Chernov,
  • E. S. Denislamova,
  • D. A. Shipilovskikh,
  • N. M. Igidov

摘要

The oxofuran ring opening of 4-substituted N′-(5-aryl-2-oxofuran-3(2H)-ylidene)-benzhydrazides upon the reaction with different alkylamines gave new modified N-alkyl-2-aroylhydrazinylidene-4-oxobutanamides. The synthesized compounds demonstrated pronounced anti-inflammatory activity in vivo and proved themselves as promising drug candidates for the treatment of inflammation.