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Synthesis and anti-influenza activity of aminoalkyl rupestonates.

Abstract
A series of aminoalkyl rupestonates were designed and synthesized by reacting rupestonic acid with 1,ω-dibromoalkanes, followed by amination. All of the new compounds were bioassayed in vitro to determine their activities against influenza A (H3N2, H1N1) and B viruses. The results showed that compounds 5a-5g, which each contain a 1H-1,2,4-triazolyl moiety, were found to be the most potent set of compounds. Compound 5g was demonstrated to possess the highest inhibitory activity against influenza H3N2 and H1N1, with IC(50) values of 0.97 and 0.42 μM, respectively. Our results also indicated that compounds 2g, 3g, 4g and 5g, which contain ten-CH(2)-unit spacers between the rupestonic acid and amino functional groups, were the most potent inhibitors of influenza H1N1 among the synthesized compounds. Unfortunately, most of the synthesized compounds did not show an obvious activity against influenza B; the only exceptions were compounds 5d and 5f, which had IC(50) values of 17.3 and 3.2 μM, respectively. Compounds 4g and 5g were potent inhibitors of influenza H1N1, and they might be potentially developed as new lead anti-influenza virus compounds. Further studies of the mechanism of action are underway.
AuthorsJiangyu Zhao, Haji Akber Aisa
JournalBioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 22 Issue 6 Pg. 2321-5 (Mar 15 2012) ISSN: 1464-3405 [Electronic] England
PMID22341943 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Ltd. All rights reserved.
Chemical References
  • Antiviral Agents
  • Azulenes
  • Sesquiterpenes
  • rupestonic acid
Topics
  • Amination
  • Animals
  • Antiviral Agents (chemical synthesis, pharmacology)
  • Azulenes (chemical synthesis, pharmacology)
  • Cell Line
  • Dogs
  • Halogenation
  • Humans
  • Influenza A Virus, H1N1 Subtype (drug effects)
  • Influenza A Virus, H3N2 Subtype (drug effects)
  • Influenza B virus (drug effects)
  • Influenza, Human (drug therapy, virology)
  • Sesquiterpenes (chemical synthesis, pharmacology)
  • Structure-Activity Relationship

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