Synthesis and pharmacological activities of some condensed 4-chloro-2,2-dialkyl chromene-3-carbaldehyde derivatives

Acta Pharm. 2008 Mar;58(1):15-27. doi: 10.2478/v10007-007-0042-4.

Abstract

Some new hydrazono 5a,b, thiosemicarbazono 6a-c, and oximo chromenes 7a-c were prepared via the reaction of the corresponding beta-chlorocarbaldehyde 3 with hydrazine, aromatic hydrazine, thiosemicarbazide and hydroxylamine hydrochloride, respectively. In addition, ether derivatives 8a-h were prepared from the corresponding aldoximes 7a-c. The new products were tested for anti-inflammatory and ulcerogenic score activities compared to indomethacin.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis*
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity
  • Benzopyrans / chemical synthesis*
  • Benzopyrans / chemistry
  • Benzopyrans / pharmacology
  • Benzopyrans / toxicity
  • Drug Design*
  • Drug Evaluation, Preclinical
  • Edema / drug therapy
  • Edema / physiopathology
  • Female
  • Lethal Dose 50
  • Male
  • Mice
  • Molecular Structure
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Stomach Ulcer / chemically induced*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Benzopyrans