Pestaloquinols A and B, isoprenylated epoxyquinols from Pestalotiopsis sp

J Nat Prod. 2011 Feb 25;74(2):286-91. doi: 10.1021/np100723t. Epub 2011 Feb 8.

Abstract

Two new isoprenylated epoxyquinol derivatives, pestaloquinols A (2) and B (3), and their putative biosynthetic precursor, cytosporin D (1), were isolated from the crude extract of the plant endophytic fungus Pestalotiopsis sp. The structures of these compounds were elucidated primarily by NMR experiments. Pestaloquinols A (2) and B (3) possess a previously undescribed nonacyclic ring system and showed cytotoxicity against HeLa cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • Benzopyrans / chemistry
  • Benzopyrans / isolation & purification*
  • Benzopyrans / pharmacology
  • Drug Screening Assays, Antitumor
  • Epoxy Compounds / chemistry
  • Epoxy Compounds / isolation & purification*
  • Epoxy Compounds / pharmacology
  • HeLa Cells
  • Humans
  • Hydroquinones / chemistry
  • Hydroquinones / isolation & purification*
  • Hydroquinones / pharmacology
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Xylariales / chemistry*

Substances

  • Antineoplastic Agents
  • Benzopyrans
  • Epoxy Compounds
  • Hydroquinones
  • cytosporin D
  • pestaloquinol A
  • pestaloquinol B