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(1-R,5-R,6-S,7-S,8-S,10-R,11-S)-6-HYDROXY-4-OXOPSEUDOGUAI-2-(3)-EN-12,8-OLIDE

Compound with spectra: 1 NMR

(1-R,5-R,6-S,7-S,8-S,10-R,11-S)-6-HYDROXY-4-OXOPSEUDOGUAI-2-(3)-EN-12,8-OLIDE
SpectraBase Compound ID FpkvfWSJwUy
InChI InChI=1S/C15H20O4/c1-7-6-10-12(8(2)14(18)19-10)13(17)15(3)9(7)4-5-11(15)16/h4-5,7-10,12-13,17H,6H2,1-3H3/t7-,8+,9+,10+,12-,13+,15+/m1/s1
InChIKey ICKWITMQEROMDG-KRPLCOHASA-N
Mol Weight 264.32 g/mol
Molecular Formula C15H20O4
Exact Mass 264.136159 g/mol
Enantiomer InChIKey ICKWITMQEROMDG-MQCIBALXSA-N

View Spectrum of (1-R,5-R,6-S,7-S,8-S,10-R,11-S)-6-HYDROXY-4-OXOPSEUDOGUAI-2-(3)-EN-12,8-OLIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
HELENALIN,11-B,13-DIHYDRO
PLENOLIN-A
Desacetyl-1-epi-isotenulin
PLENOLIN
TENULIN,DESACETYL,1-EPI,ISO
DESACETYL-ISOTENULIN
Desacetyl-1-epi-isotenulin
Tetrahydro-1-epi-allohelenalin
4-Oxo-6-hydroxy-pseudoguai-11(13)-en-8,12-olide
PSEUDOGUAI-11(13)-EN-12,8-A-OLISE,6-A-HYDROXY-4-OXO
3-Oxo-14-hydro-5.alpha.,4,6,11beta.-eudesman-12,6-olide methyl acetal
AULACOCARPINOLIDE
CORONALACTONE
Title Journal or Book Year
Pseudoguaianolides and Guaianolides from Inula hupehensis as Potential Anti-inflammatory Agents Journal of Natural Products 2011

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