Marilines A-C: novel phthalimidines from the sponge-derived fungus Stachylidium sp

Chemistry. 2012 Jul 9;18(28):8827-34. doi: 10.1002/chem.201103278. Epub 2012 Jun 18.

Abstract

A marine-derived fungus of the genus Stachylidium was isolated from the sponge Callyspongia cf. C. flammea. Chemical investigation of the bioactive fungal extract led to the isolation of the novel phthalimidine derivatives marilines A(1) (1a), A(2) (1b), B (2), and C (3). The absolute configurations of the enantiomeric compounds 1a and 1b were assigned by a combination of experimental circular dichroism (CD) investigations and quantum chemical CD calculations. The skeleton of marilines is most unusual, and its biosynthesis is suggested to require uncommon biochemical reactions in fungal secondary metabolism. Both enantiomers, marilines A(1) (1a) and A(2) (1b), inhibited human leukocyte elastase (HLE) with an IC(50) value of 0.86 μM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ascomycota / chemistry*
  • Humans
  • Leukocyte Elastase / antagonists & inhibitors*
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Phthalimides / chemistry
  • Phthalimides / isolation & purification*
  • Phthalimides / pharmacology
  • Porifera / microbiology*

Substances

  • Phthalimides
  • mariline A
  • mariline B
  • mariline C
  • phthalimidine
  • Leukocyte Elastase