InChI=1S/C20H24O6/c1-6-9(2)18(22)25-14-7-10(3)16-13(21)8-11(4)20(16,24)17-15(14)12(5)19(23)26-17/h6,11,14-15,17,24H,5,7-8H2,1-4H3/b9-6+/t11-,14+,15-,17+,20-/m1/s1 |
SKWQNPANRJEPQJ-JTOVZCNQSA-N |
[H][C@@]12[C@H](CC(C)=C3C(=O)C[C@@H](C)[C@]3(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
root
(BTO:0001188).
See:
PubMed
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Elephantopus mollis
(NCBI:txid318057)
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Found in
stem
(BTO:0001300).
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)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
has functional parent
tiglic acid
(CHEBI:9592)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
has role
antineoplastic agent
(CHEBI:35610)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
has role
metabolite
(CHEBI:25212)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
is a
γ-lactone
(CHEBI:37581)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
is a
enoate ester
(CHEBI:51702)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
is a
guaiane sesquiterpenoid
(CHEBI:36744)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
is a
organic heterotricyclic compound
(CHEBI:26979)
(4βH)-5α-hydroxy-8α-(2-methylbut-2-enoyloxy)-2-oxo-1(10),11(13)-guaiadien-12,6α-olide
(CHEBI:65832)
is a
tertiary alcohol
(CHEBI:26878)
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(3aR,4S,9R,9aR,9bS)-9a-hydroxy-6,9-dimethyl-3-methylidene-2,7-dioxo-2,3,3a,4,5,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-4-yl (2E)-2-methylbut-2-enoate
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18556305
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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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