InChI=1S/C32H46O8/c1-17(33)40-27(2,3)13-12-23(36)32(9,39)25-21(35)15-29(6)22-11-10-18-19(14-20(34)26(38)28(18,4)5)31(22,8)24(37)16-30(25,29)7/h10,12-13,19-22,25,34-35,39H,11,14-16H2,1-9H3/b13-12+/t19-,20+,21-,22+,25+,29+,30-,31+,32+/m1/s1 |
IXQKXEUSCPEQRD-DKRGWESNSA-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)OC(C)=O)[C@@]3(C)CC(=O)[C@@]21C |
|
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 )
|
|
View more via ChEBI Ontology
(2S,4R,23E)-2,16β,20-trihydroxy-9β,10,14-trimethyl-1,11,22-trioxo-4,9-cyclo-9,10-secocholesta-5,23-dien-25-yl acetate
|
1,2-dihydro-α-elaterin
|
ChemIDplus
|
2β,16α,20,25-tetrahydroxy-9-methyl-19-nor-9β,10α-lanosta-5,23-diene-3,11,22-trione, 25-acetate
|
ChemIDplus
|
2β,16α,20,25-tetrahydroxy-9-methyl-3,11,22-trioxo-19-nor-9β,10α-lanosta-5,23-dien-25-yl acetate
|
ChEBI
|
cucurbitacin B
|
UniProt
|
2068869
|
Reaxys Registry Number
|
Reaxys
|
6199-67-3
|
CAS Registry Number
|
ChemIDplus
|
18309509
|
PubMed citation
|
Europe PMC
|
18442812
|
PubMed citation
|
Europe PMC
|
18561312
|
PubMed citation
|
Europe PMC
|
19700240
|
PubMed citation
|
Europe PMC
|
20153103
|
PubMed citation
|
Europe PMC
|
20483353
|
PubMed citation
|
Europe PMC
|
21344491
|
PubMed citation
|
Europe PMC
|
4384331
|
PubMed citation
|
Europe PMC
|
5640163
|
PubMed citation
|
Europe PMC
|
|