InChI=1S/C30H44O7/c1-25(2,36)12-11-21(33)30(8,37)23-19(32)14-27(5)20-10-9-16-17(13-18(31)24(35)26(16,3)4)29(20,7)22(34)15-28(23,27)6/h9,11-12,17-20,23,31-32,36-37H,10,13-15H2,1-8H3/b12-11+/t17-,18+,19-,20+,23+,27+,28-,29+,30+/m1/s1 |
SRPHMISUTWFFKJ-QJNWWGCFSA-N |
[H][C@@]12C[C@H](O)C(=O)C(C)(C)C1=CC[C@@]1([H])[C@]3(C)C[C@@H](O)[C@]([H])([C@@](C)(O)C(=O)\C=C\C(C)(C)O)[C@@]3(C)CC(=O)[C@@]21C |
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allelochemical
A class of secondary metabolites developed by many plants to influence the behaviour, growth or survival of herbivores, and thus acting as a defence against herbivory.
(via cucurbitacin )
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View more via ChEBI Ontology
(2S,4R,23E)-2,16,20,25-tetrahydroxy-9β,10,14-trimethyl-4,9-cyclo-9,10-seco-16α-cholesta-5,23-diene-1,11,22-trione
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(23E)-2β,16α,20,25- tetrahydroxy-9β-methyl-19-nor-10α-lanosta-5,23-diene-3,11,22-trione
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ChEBI
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(23E)-2β,16α,20,25-tetrahydroxy-10α-cucurbita-5,23-diene-3,11,22-trione
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ChEBI
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Elatericin A
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ChemIDplus
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Elatericine A
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ChemIDplus
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2068583
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Reaxys Registry Number
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Reaxys
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3877-86-9
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CAS Registry Number
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ChemIDplus
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19185617
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PubMed citation
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Europe PMC
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20926322
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PubMed citation
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Europe PMC
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21184524
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PubMed citation
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Europe PMC
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4384331
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PubMed citation
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Europe PMC
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8858910
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PubMed citation
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Europe PMC
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