Isolation and structures of pipecolidepsins A and B, cytotoxic cyclic depsipeptides from the Madagascan sponge Homophymia lamellosa

J Nat Prod. 2014 Feb 28;77(2):298-303. doi: 10.1021/np400888e. Epub 2014 Jan 24.

Abstract

Two new cyclic depsipeptides, pipecolidepsins A and B (1 and 2), have been isolated from the sponge Homophymia lamellosa collected off the coast of Madagascar. Their structures were determined by a combination of NMR experiments and by LC-MS analysis of the amino acid fragments obtained by hydrolysis and derivatization using Marfey's reagent. In addition to several common amino acids, these peptides contain unusual residues, including 2-amino-3-hydroxy-4,5-dimethylhexanoic acid, 3-ethoxyasparagine, 3,4-dimethylglutamine, 4,7-diamino-2,3-dihydroxy-7-oxoheptanoic acid, and 3-hydroxyaspartic acid as well as a terminal 3-hydroxy-2,4,6-trimethylheptanoic acid residue. Pipecolidepsins A and B displayed cytotoxic activity against a panel of different human tumor cell lines.

MeSH terms

  • Animals
  • Aspartic Acid / analogs & derivatives
  • Depsipeptides / chemistry
  • Depsipeptides / isolation & purification*
  • Drug Screening Assays, Antitumor
  • Glutamine / analogs & derivatives
  • Humans
  • Madagascar
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Porifera / chemistry*

Substances

  • 3,4-dimethylglutamine
  • Depsipeptides
  • pipecolidepsin A
  • pipecolidepsin B
  • Glutamine
  • 3-hydroxyaspartic acid
  • Aspartic Acid