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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