InChI=1S/C36H52O12/c1- 31(2) 16- 9- 10- 21- 33(5) 13- 19- 28(36(8,45) 22(38) 12- 24(46- 19) 32(3,4) 44) 34(33,6) 14- 23(39) 35(21,7) 17(16) 11- 18(29(31) 43) 47- 30- 27(42) 26(41) 25(40) 20(15- 37) 48- 30/h9,11,17,19- 21,24- 28,30,37,40- 42,44- 45H,10,12- 15H2,1- 8H3/t17- ,19- ,20- ,21+,24+,25- ,26+,27- ,28+,30- ,33+,34- ,35+,36+/m1/s1 |
IWNXFVRPEIWIJJ-VPLPWDSJSA-N |
[H] [C@@] 12C[C@@] 3(C) [C@] 4([H] ) CC=C5[C@@] ([H] ) (C=C(O[C@@H] 6O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H] 6O) C(=O) C5(C) C) [C@] 4(C) C(=O) C[C@] 3(C) [C@@] 1([H] ) [C@@] (C) (O) C(=O) C[C@H] (O2) C(C) (C) O |
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Machilus yaoshansis
(NCBI:txid251260)
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Found in
root
(BTO:0001188).
Ethanolic extract of air-dried and powdered roots
See:
PubMed
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via (16alpha,20R,24S)-16,24-epoxy-2,20,25-trihydroxycucurbita-1,5-diene-3,11,22-trione 2-O-beta-D-glucopyranoside )
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
Outgoing
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(16alpha,20R,24S)- 16,24- epoxy- 2,20,25- trihydroxycucurbita- 1,5- diene- 3,11,22- trione 2- O- beta- D- glucopyranoside
(CHEBI:68909)
has role
metabolite
(CHEBI:25212)
(16alpha,20R,24S)- 16,24- epoxy- 2,20,25- trihydroxycucurbita- 1,5- diene- 3,11,22- trione 2- O- beta- D- glucopyranoside
(CHEBI:68909)
is a
cucurbitacin
(CHEBI:16219)
(16alpha,20R,24S)- 16,24- epoxy- 2,20,25- trihydroxycucurbita- 1,5- diene- 3,11,22- trione 2- O- beta- D- glucopyranoside
(CHEBI:68909)
is a
glycoside
(CHEBI:24400)
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22044245
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PubMed citation
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Europe PMC
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