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CHEBI:145029 - steviolmonoside

ChEBI IDCHEBI:145029
ChEBI Namesteviolmonoside
Stars
DefinitionA β-D-glucoside resulting from the formal condensation the tertiary allylic hydroxy group of steviol with β-D-glucopyranose.
Last Modified22 August 2023
SubmitterGareth Owen
DownloadsMolfile
FormulaC26H40O8
Net Charge0
Average Mass480.598
Monoisotopic Mass480.27232
SMILES[H][C@]12CC[C@]34CC(=C)[C@](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)(CC[C@@]3([H])[C@]1(C)CCC[C@@]2(C)C(=O)O)C4
InChIInChI=1S/C26H40O8/c1-14-11-25-9-5-16-23(2,7-4-8-24(16,3)22(31)32)17(25)6-10-26(14,13-25)34-21-20(30)19(29)18(28)15(12-27)33-21/h15-21,27-30H,1,4-13H2,2-3H3,(H,31,32)/t15-,16+,17+,18-,19+,20-,21+,23-,24-,25-,26+/m1/s1
InChIKeyQSIDJGUAAUSPMG-CULFPKEHSA-N
Species of MetaboliteComponentSourceComments
Stevia rebaudiana (ncbitaxon:55670) - PubMed (17397883)
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
ChEBI Ontology
Outgoing Relation(s)
steviolmonoside (CHEBI:145029) has functional parent steviol (CHEBI:145024)
steviolmonoside (CHEBI:145029) is a ent-kaurane diterpenoid (CHEBI:36760)
steviolmonoside (CHEBI:145029) is a bridged compound (CHEBI:35990)
steviolmonoside (CHEBI:145029) is a diterpene glycoside (CHEBI:71939)
steviolmonoside (CHEBI:145029) is a monocarboxylic acid (CHEBI:25384)
steviolmonoside (CHEBI:145029) is a tetracyclic diterpenoid (CHEBI:52557)
steviolmonoside (CHEBI:145029) is a β-D-glucoside (CHEBI:22798)
steviolmonoside (CHEBI:145029) is conjugate acid of steviolmonoside(1−) (CHEBI:145010)
Incoming Relation(s)
steviolbioside (CHEBI:145030) has functional parent steviolmonoside (CHEBI:145029)
steviolmonoside(1−) (CHEBI:145010) is conjugate base of steviolmonoside (CHEBI:145029)
IUPAC Name 
13α-(β-D-glucopyranosyloxy)-5β,8α,9β,10α-kaur-16-en-18-oic acid
Synonyms  Source
glucosilsteviolChemIDplus
steviolmonosideChemIDplus
13-O-beta-D-glucopyranosyl steviolChemIDplus
13-O-β-D-glucopyranosyl steviolChemIDplus
steviol-13-O-D-glucopyranosideChEBI
Manual XrefsDatabases
CPD-14502MetaCyc
C00034697KNApSAcK
Registry NumbersSources
CAS:60129-60-4ChemIDplus
Citations