CHEBI:68383 - stigmasterol 3-O-β-D-glucoside

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ChEBI Name stigmasterol 3-O-β-D-glucoside
ChEBI ASCII Name stigmasterol 3-O-beta-D-glucoside
Definition A steroid saponin that is (3β,22E)-stigmasta-5,22-dien-3-ol attached to a β-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It is isolated from Symplocos lancifolia.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C35H58O6
Net Charge 0
Average Mass 574.83140
Monoisotopic Mass 574.42334
InChI InChI=1S/C35H58O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h8-10,20-22,24-33,36-39H,7,11-19H2,1-6H3/b9-8+/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1
SMILES [H][C@@]1(O[C@H]2CC[C@@]3(C)C(C2)=CC[C@]2([H])[C@]3([H])CC[C@]3(C)[C@]([H])(CC[C@@]23[H])[C@H](C)\C=C\[C@@H](CC)C(C)C)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Metabolite of Species Details
Symplocos lancifolia (NCBI:txid239704) Found in leaf (BTO:0000713). Dried, powdered leaves extracted with boiling 80% methanol See: PubMed
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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing stigmasterol 3-O-β-D-glucoside (CHEBI:68383) has functional parent stigmasterol (CHEBI:28824)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) has parent hydride stigmastane (CHEBI:26773)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) has role metabolite (CHEBI:25212)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) is a β-D-glucoside (CHEBI:22798)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) is a monosaccharide derivative (CHEBI:63367)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) is a phytosterols (CHEBI:26125)
stigmasterol 3-O-β-D-glucoside (CHEBI:68383) is a steroid saponin (CHEBI:61655)
(3β,22E)-stigmasta-5,22-dien-3-yl β-D-glucopyranoside
Synonym Source
stigmasteryl 3-β-D-glucoside UniProt
Registry Number Type Source
4302422 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21288041 PubMed citation Europe PMC
Last Modified
15 November 2019