InChI=1S/C20H22O5/c1- 6- 9(2) 19(22) 24- 14- 8- 11(4) 15- 13(21) 7- 10(3) 16(15) 18- 17(14) 12(5) 20(23) 25- 18/h6,10,14,17- 18H,4- 5,7- 8H2,1- 3H3/b9- 6+/t10- ,14+,17- ,18- /m1/s1 |
QFLXCTZTPACOEB-MIQTUIGVSA-N |
[H][C@@]12[C@H](CC(=C)C3=C([C@H](C)CC3=O)[C@H]1OC(=O)C2=C)OC(=O)C(\C)=C\C |
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Elephantopus mollis
(NCBI:txid318057)
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Found in
stem
(BTO:0001300).
See:
PubMed
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Elephantopus mollis
(NCBI:txid318057)
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Found in
root
(BTO:0001188).
See:
PubMed
|
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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View more via ChEBI Ontology
Outgoing
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(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
has functional parent
tiglic acid
(CHEBI:9592)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
has role
antineoplastic agent
(CHEBI:35610)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
has role
metabolite
(CHEBI:25212)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
is a
γ-lactone
(CHEBI:37581)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
is a
enoate ester
(CHEBI:51702)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
is a
enone
(CHEBI:51689)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
is a
guaiane sesquiterpenoid
(CHEBI:36744)
(4βH)- 8α- (2- methylbut- 2- enoyloxy)- 2- oxo- 1(5),10(14),11(13)- guaiatrien- 12,6α- olide
(CHEBI:65833)
is a
organic heterotricyclic compound
(CHEBI:26979)
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(3aR,4S,9R,9bS)- 9- methyl- 3,6- dimethylidene- 2,7- dioxo- 2,3,3a,4,5,6,7,8,9,9b- decahydroazuleno[4,5- b]furan- 4- yl (2E)- 2- methylbut- 2- enoate
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18556304
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Reaxys Registry Number
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Reaxys
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18239317
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PubMed citation
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Europe PMC
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