Marine natural meroterpenes: synthesis and antiproliferative activity

Mar Drugs. 2010 Feb 23;8(2):347-58. doi: 10.3390/md8020347.

Abstract

Meroterpenes are compounds of mixed biogenesis, isolated from plants, microorganisms and marine invertebrates. We have previously isolated and determined the structure for a series of meroterpenes extracted from the ascidian Aplidium aff. densum. Here, we demonstrate the chemical synthesis of three of them and their derivatives, and evaluate their biological activity on two bacterial strains, on sea urchin eggs, and on cancerous and healthy human cells.

Keywords: antiproliferative activity; didehydroconicol; epiconicol; meroterpene; methoxyconidiol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abietanes / chemical synthesis
  • Abietanes / pharmacology*
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Benzopyrans / chemical synthesis
  • Benzopyrans / pharmacology*
  • Cell Proliferation / drug effects
  • Humans
  • Hydroquinones / chemical synthesis
  • Hydroquinones / pharmacology*
  • Sea Urchins
  • Structure-Activity Relationship
  • Terpenes / chemical synthesis
  • Terpenes / pharmacology*
  • Urochordata / chemistry*

Substances

  • Abietanes
  • Anti-Bacterial Agents
  • Benzopyrans
  • Hydroquinones
  • Terpenes
  • conicol
  • didehydroconicol
  • methoxyconidiol