New verticillane diterpenoids from Cespitularia taeniata

Chem Biodivers. 2012 Mar;9(3):654-61. doi: 10.1002/cbdv.201100122.

Abstract

Chemical investigation of Cespitularia taeniata has led to the isolation of three new verticillanes, cespitulins E-G (1-3, resp.). The structures of these compounds were elucidated by spectroscopic analysis, especially HR-MS and 2D-NMR techniques. Compound 1 possesses a rare norverticillane skeleton with two adjacent OH groups at C(5) and C(6), while the seco-compound 2 with an aldehyde group at C(9) results from an unusual bond cleavage between C(9) and C(10). Pharmacological studies revealed that compound 3 exhibited significant activities on superoxide-anion generation and elastase release by human neutrophils in response to FMLP/CB. A plausible biogenetic pathway for compound 2 is also discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthozoa / chemistry*
  • Diterpenes / chemistry*
  • Diterpenes / isolation & purification
  • Diterpenes / pharmacology
  • Humans
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Molecular Conformation
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Pancreatic Elastase / metabolism
  • Superoxides / metabolism

Substances

  • Diterpenes
  • cespitulin E
  • cespitulin F
  • cespitulin G
  • verticillane
  • Superoxides
  • Pancreatic Elastase