Biological effects of prenylated hydroquinones: structure-activity relationship studies in antimicrobial, brine shrimp, and fish lethality assays

J Nat Prod. 1994 Dec;57(12):1711-6. doi: 10.1021/np50114a015.

Abstract

Twenty-three hydroquinone and quinone derivatives were assayed for antimicrobial effects and brine shrimp and fish lethalities, to establish relevant structure-activity relationships (SAR). Linear 2-prenyl-1,4-hydroquinones used for bioassay were obtained either by isolation from the sponge Ircinia spinosula or by synthesis. Corresponding quinones, as well as hydroquinones possessing saturated side-chains composed of one to eight isopentane units, were also synthesized and biologically evaluated. Terpenoid 1,4-benzoquinones displayed moderate antimicrobial activity against three microorganisms, SAR studies indicate the optimum length of the side-chain is in the range of five to fifteen carbon atoms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology*
  • Anti-Infective Agents / toxicity
  • Artemia
  • Bacteria / drug effects*
  • Cyprinodontiformes / physiology*
  • Drug Screening Assays, Antitumor
  • Fungi / drug effects*
  • Hydroquinones / chemistry
  • Hydroquinones / pharmacology*
  • Hydroquinones / toxicity
  • Microbial Sensitivity Tests
  • Porifera / chemistry*
  • Structure-Activity Relationship
  • Terpenes / chemistry
  • Terpenes / pharmacology*
  • Terpenes / toxicity

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Hydroquinones
  • Terpenes