CHEBI:59030 - oleandrin

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ChEBI Name oleandrin
Definition A steroid saponin that consists of oleandrigenin having a 2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl residue attached to the oxygen function at position 3.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C32H48O9
Net Charge 0
Average Mass 576.71810
Monoisotopic Mass 576.32983
InChI InChI=1S/C32H48O9/c1-17-29(35)24(37-5)14-27(39-17)41-21-8-10-30(3)20(13-21)6-7-23-22(30)9-11-31(4)28(19-12-26(34)38-16-19)25(40-18(2)33)15-32(23,31)36/h12,17,20-25,27-29,35-36H,6-11,13-16H2,1-5H3/t17-,20+,21-,22-,23+,24-,25-,27-,28-,29-,30-,31+,32-/m0/s1
SMILES [H][C@]12CC[C@]3([H])[C@]([H])(CC[C@]4(C)[C@H]([C@H](C[C@]34O)OC(C)=O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](OC)[C@@H](O)[C@H](C)O1
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 oleandrin (CHEBI:59030) has functional parent oleandrigenin (CHEBI:63508)
oleandrin (CHEBI:59030) is a 14β-hydroxy steroid (CHEBI:36862)
oleandrin (CHEBI:59030) is a cardenolide glycoside (CHEBI:38092)
oleandrin (CHEBI:59030) is a steroid ester (CHEBI:47880)
oleandrin (CHEBI:59030) is a steroid saponin (CHEBI:61655)
Synonyms Sources
Foliandrin ChemIDplus
Folinerin ChemIDplus
Neriolin ChemIDplus
Neriostene ChemIDplus
Oleandrina ChemIDplus
Manual Xrefs Databases
3399 DrugCentral
Oleandrin Wikipedia
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Registry Numbers Types Sources
101529 Reaxys Registry Number Reaxys
465-16-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10438974 PubMed citation Europe PMC
23073998 PubMed citation Europe PMC
24172227 PubMed citation Europe PMC
24375780 PubMed citation Europe PMC
24431454 PubMed citation Europe PMC
26444270 PubMed citation Europe PMC
Last Modified
22 February 2017