Microwave assisted synthesis and anti-influenza virus activity of 1-adamantyl substituted N-(1-thia-4-azaspiro[4.5]decan-4-yl)carboxamide derivatives

Goktas F., Vanderlinden E., Naesens L., Cesur N., Cesur Z.

BIOORGANIC & MEDICINAL CHEMISTRY, vol.20, no.24, pp.7155-7159, 2012 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 20 Issue: 24
  • Publication Date: 2012
  • Doi Number: 10.1016/j.bmc.2012.09.064
  • Journal Name: BIOORGANIC & MEDICINAL CHEMISTRY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.7155-7159
  • Keywords: Adamantane, Spirothiazolidinone, Microwave, Antiviral, Influenza virus, Hemagglutinin, INFLUENZA-A VIRUS, HEMAGGLUTININ, INHIBITORS, AGENTS
  • Istanbul University Affiliated: Yes

Abstract

A microwave-assisted three-component one-pot cyclocondensation method was applied for the synthesis of novel N-(1-thia-4-azaspiro[4.5] decan-4-yl)carboxamide compounds carrying an adamantyl moiety. The structures of the compounds were confirmed by spectral and elemental analysis. All compounds were evaluated for antiviral activity against influenza A (H1N1 and H3N2) and influenza B virus in MDCK cell cultures. The compounds displayed a confined structure-activity relationship. The N-(2,8-dimethyl-3-oxo-1-thia-4-azaspiro[4.5] dec-4-yl)adamantane-1-carboxamide 3b was the most potent inhibitor [antiviral EC50: 1.4 mu M against influenza A/H3N2 virus]. Its strong inhibitory effect in a virus hemolysis assay supports that 3b acts as an influenza virus fusion inhibitor by preventing the conformational change of the influenza virus hemagglutinin at low pH. (C) 2012 Elsevier Ltd. All rights reserved.