CHEBI:63514 - erysimoside

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ChEBI Name erysimoside
ChEBI ID CHEBI:63514
Definition A cardenolide glycoside that consists of strophanthidin having a β-D-glucopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl moiety attached at position 3.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C35H52O14
Net Charge 0
Average Mass 696.77900
Monoisotopic Mass 696.33571
InChI InChI=1S/C35H52O14/c1-17-30(49-31-29(42)28(41)27(40)24(14-36)48-31)23(38)12-26(46-17)47-19-3-8-33(16-37)21-4-7-32(2)20(18-11-25(39)45-15-18)6-10-35(32,44)22(21)5-9-34(33,43)13-19/h11,16-17,19-24,26-31,36,38,40-44H,3-10,12-15H2,1-2H3/t17-,19+,20-,21+,22-,23+,24-,26+,27-,28+,29-,30-,31+,32-,33+,34+,35+/m1/s1
InChIKey KQBVSIZPUWODNU-VRQSBXMXSA-N
SMILES [H][C@@]1(CC[C@]2(O)[C@]3([H])CC[C@]4(O)C[C@H](CC[C@]4(C=O)[C@@]3([H])CC[C@]12C)O[C@H]1C[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](C)O1)C1=CC(=O)OC1
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via saponin )
Application(s): cardioprotective agent
Any protective agent that is able to prevent damage to the heart.
(via cardiac glycoside )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing erysimoside (CHEBI:63514) has functional parent strophanthidin (CHEBI:38178)
erysimoside (CHEBI:63514) is a 14β-hydroxy steroid (CHEBI:36862)
erysimoside (CHEBI:63514) is a 19-oxo steroid (CHEBI:38149)
erysimoside (CHEBI:63514) is a 5β-hydroxy steroid (CHEBI:38195)
erysimoside (CHEBI:63514) is a cardenolide glycoside (CHEBI:38092)
erysimoside (CHEBI:63514) is a steroid aldehyde (CHEBI:131565)
erysimoside (CHEBI:63514) is a steroid saponin (CHEBI:61655)
IUPAC Name
(3β,5β)-3-{[β-D-glucopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl]oxy}-5,14-dihydroxy-19-oxocard-20(22)-enolide
Synonyms Sources
(3β,5β)-3-{[2,6-dideoxy-4-O-(β-D-glucopyranosyl)-β-D-ribo-hexopyranosyl]oxy}-5,14-dihydroxy-19-oxocard-20(22)-enolide IUPAC
Erizimoside ChemIDplus
Neoglucoerysimoside ChemIDplus
strophanthidin digilanobioside ChEBI
Registry Numbers Types Sources
7082-34-0 CAS Registry Number ChemIDplus
79099 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1218612 PubMed citation Europe PMC
14264100 PubMed citation Europe PMC
7739045 PubMed citation Europe PMC
Last Modified
17 March 2016