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(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone |
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CHEBI:70554 |
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(+)-(5S,6S,7S,8R,10R)-6-hydroxy-7,8-epoxy-12-oxo-abieta-9(11),13-dien-20-oic acid 6,20-lactone |
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An abietane diterpenoid isolated from the stem bark of Fraxinus sieboldiana. |
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![](images/goldenstar.gif) ![](images/goldenstar.gif)
This entity has been manually annotated by the ChEBI Team.
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Molfile
XML
SDF
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InChI=1S/C20H24O4/c1- 10(2) 11- 9- 20- 13(8- 12(11) 21) 19- 7- 5- 6- 18(3,4) 15(19) 14(16(20) 24- 20) 23- 17(19) 22/h8- 10,14- 16H,5- 7H2,1- 4H3/t14- ,15- ,16- ,19- ,20+/m0/s1 |
CMURQFGSNXTIKZ-IEYYFSCXSA-N |
CC(C)C1=C[C@]23O[C@H]2[C@H]2OC(=O)[C@@]4(CCCC(C)(C)[C@H]24)C3=CC1=O |
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Fraxinus sieboldiana
(NCBI:txid490850)
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Found in
stem
(BTO:0001300).
Previous component: stem bark; EtOAc soluble fraction of 95% ethanolic extract of air-dried stem bark
See:
PubMed
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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View more via ChEBI Ontology
Outgoing
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(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone
(CHEBI:70554)
has role
plant metabolite
(CHEBI:76924)
(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone
(CHEBI:70554)
is a
abietane diterpenoid
(CHEBI:36762)
(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone
(CHEBI:70554)
is a
cyclic terpene ketone
(CHEBI:36130)
(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone
(CHEBI:70554)
is a
diterpene lactone
(CHEBI:49193)
(+)- (5S,6S,7S,8R,10R)- 6- hydroxy- 7,8- epoxy- 12- oxo- abieta- 9(11),13- dien- 20- oic acid 6,20- lactone
(CHEBI:70554)
is a
epoxide
(CHEBI:32955)
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(4aR,5aS,6S,6aS,10aR)- 7,7- dimethyl- 3- (propan- 2- yl)- 6,6a,7,8,9,10- hexahydro- 2H,5aH- 6,10a- (epoxymethano)phenanthro[8a,9- b]oxirene- 2,11- dione
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21097459
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Reaxys Registry Number
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Reaxys
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20961093
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PubMed citation
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Europe PMC
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