|
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide |
|
CHEBI:69326 |
|
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide |
|
A pseudoguaianolide with anti-inflammatory activity isolated from the aerial parts of Inula hupehensis. |
|
This entity has been manually annotated by the ChEBI Team.
|
|
|
|
Molfile
XML
SDF
|
|
|
|
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 |
ICKWITMQEROMDG-KRPLCOHASA-N |
C[C@H]1[C@@H]2[C@H](C[C@@H](C)[C@@H]3C=CC(=O)[C@@]3(C)[C@H]2O)OC1=O |
|
Inula hupehensis
(IPNI:225932-1)
|
Found in
aerial part
(BTO:0001658).
95% aqueous EtOH extract of dried and powdered aerial parts
See:
PubMed
|
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
|
|
anti-inflammatory agent
Any compound that has anti-inflammatory effects.
|
|
View more via ChEBI Ontology
Outgoing
|
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
has role
anti-inflammatory agent
(CHEBI:67079)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
has role
plant metabolite
(CHEBI:76924)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
is a
γ-lactone
(CHEBI:37581)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
is a
cyclic ketone
(CHEBI:3992)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
is a
organic heterotricyclic compound
(CHEBI:26979)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
is a
pseudoguaianolide
(CHEBI:76704)
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide
(CHEBI:69326)
is a
secondary alcohol
(CHEBI:35681)
|
|
(3S,3aS,4S,4aR,7aR,8R,9aS)-4-hydroxy-3,4a,8-trimethyl-3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione
|
21902549
|
Reaxys Registry Number
|
Reaxys
|
21894898
|
PubMed citation
|
Europe PMC
|
|