Compound
rebaudioside M
A rebaudioside that is rebaudioside A in which the the hydroxy groups at positions 2 and 3 of the β-D-glucosyl ester moiety have both been converted to the corresponding β-D-glucoside. Found in very low concentraitions in the leaves of Stevia Rebaudiana, it is more than 200 times sweeter than sucrose.
Definition from ChEBI (CHEBI:145019), read 2026-09-23. CC BY 4.0.
CHEBI:145019ChEBI
Structure
No three-dimensional record for this entry.
- Class
- Organic compound
- Formula
- C56H90O33
- Mass
- 1291.303 g/mol
- Charge
- 0
- InChIKey
- GSGVXNMGMKBGQU-PHESRWQRSA-N
- SMILES
- [H][C@]12CC[C@]34CC(=C)[C@](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@H]5O[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[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C4
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
What the reference databases state
Chemical structure
- rebaudioside M has the functional parent rebaudioside ACompoundChEBI CHEBI:145019Inferred only
- rebaudioside M has the functional parent rebaudioside DCompoundChEBI CHEBI:145019Inferred only
Reactions
1 reaction
rebaudioside D+UDP-alpha-D-glucoserebaudioside M+UDP+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:61776CC BY 4.0Reference data
Other names
7 names
Resolves to: rebaudioside M
- Also called
- Reb MReb XReb-MReb-Xrebaudioside X
- Systematic name
- beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-1-O-(13alpha-{[beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-glucopyranosyl]oxy}-18-oxo-5beta,8alpha,9beta,10alpha-kaur-16-en-18-yl)-beta-D-glucopyranoseβ-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-1-O-(13α-{[β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl]oxy}-18-oxo-5β,8α,9β,10α-kaur-16-en-18-yl)-β-D-glucopyranose