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Costunolide

Catalog No. Bio-0308 Name InterBioScreen
CAS Number 553-21-9 Website http://www.ibscreen.com
M. F. C15H20O2 Telephone +7 49652 40091
M. W. 232.3181 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 126716

SYNONYMS

IUPAC name
(3aS,11aR)-6,10-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-2-one
IUPAC Traditional name
(3aS,11aR)-6,10-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-2-one

DATABASE IDS

CAS Number 553-21-9

PROPERTIES

Application(s) Shows antimycobacterial activity
Biological Source Constit. of costus root (Saussurea lappa) and Artemisia balchanorum. Also from Talauma mexicana and Cosmos sulphureus
Mechanism of Action Suppressive on cytotoxic T lymphocytes
Mechanism of Action Effective HO-1 inducer inhibiting macrophage-derived pro-inflammatory cytokines
Mechanism of Action Activator of Nrf2 leading to HO-1 expression

DETAILS

REFERENCES

  • Rao, A.S. et al., Tetrahedron, 1960, 9, 275, (isol)
  • Bouill, M.J. et al., Acta Cryst. B, 1976, 32, 3203, (cryst struct)
  • Kanasaki, T. et al., Agric. Biol. Chem., 1976, 40, 1239
  • Grieco, P.A. et al., J.O.C., 1977, 42, 1717, (synth)
  • Shibuya, H. et al., Chem. Lett., 1986, 85, (synth)
  • Takahashi, T. et al., Tetrahedron, 1987, 43, 5499, (synth)
  • Banerjee, A.K. et al., Tetrahedron, 1993, 49, 4761, (synth, rev)
  • Taniguchi, M. et al., Biosci., Biotechnol., Biochem., 1995, 59, 2064-2067, (activity)
  • Jacobsson, U. et al., Phytochemistry, 1995, 39, 839, (Costunolide, pmr, cmr)
  • Park, H.-J. et al., J. Nat. Prod., 1996, 59, 1128, (Costunolide, pmr, cmr)
  • Fischer, N.H. et al., Phytochemistry, 1998, 49, 559-564, (activity)
  • Jang, D.S. et al., Saengyak Hakhoechi, 1998, 29, 67-70, (activity)