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Synthesis and anti-inflammatory activity of three nitro chalcones.

Abstract
The aim of this study was to synthesize three nitro substituted chalcones and to evaluate their anti-inflammatory activity in the model of carrageenan induced edema in rats. The nitro chalcone were prepared by aldol condensation using of mechanical agitation and environmentally friendly solvents with 72-73% yields in approximately 2h. The three structures were evaluated on biological activity at dose of 200mg/kg and they showed anti-inflammatory protective effect by both oral and intraperitoneal administration, this effect was time dependent.
AuthorsAbraham Gómez-Rivera, Hidemí Aguilar-Mariscal, Nancy Romero-Ceronio, Luis F Roa-de la Fuente, Carlos E Lobato-García
JournalBioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 23 Issue 20 Pg. 5519-22 (Oct 15 2013) ISSN: 1464-3405 [Electronic] England
PMID24012185 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 The Authors. Published by Elsevier Ltd.. All rights reserved.
Chemical References
  • Anti-Inflammatory Agents
  • Chalcone
Topics
  • Administration, Oral
  • Animals
  • Anti-Inflammatory Agents (chemical synthesis, chemistry, therapeutic use)
  • Area Under Curve
  • Chalcone (chemical synthesis, chemistry, therapeutic use)
  • Disease Models, Animal
  • Edema (chemically induced, drug therapy)
  • ROC Curve
  • Rats

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