Compound
apigenin 7-O-beta-D-glucoside
A flavonoid oxoanion that is the conjugate base of apigenin 7-O-β-D-glucoside, obtained by deprotonation of the 7-hydroxy group. Major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
Definition from ChEBI (CHEBI:77722), read 2026-09-23. CC BY 4.0.
Structure
- Class
- Organic compound, anion
- Formula
- C21H19O10
- Mass
- 431.373 g/mol
- Charge
- -1
- InChIKey
- KMOUJOKENFFTPU-QNDFHXLGSA-M
- SMILES
- O=c1cc(-c2ccc(O)cc2)oc2cc(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)cc([O-])c12
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
1 statement
1 statement · 1 reference database · Subject: apigenin 7-O-beta-D-glucoside · Sources: Rhea
- apigenin 7-O-beta-D-glucoside is a substrate of LCTProteinRhea RHEA:69679Inferred only
Reactions
4 reactions
CHEBI:73883+apigenin 7-O-beta-D-glucosideCHEBI:77640+UDP+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:19153CC BY 4.0Reference data
apigenin+UDP-alpha-D-glucoseapigenin 7-O-beta-D-glucoside+UDP+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:59760CC BY 4.0Reference data
apigenin 7-O-beta-D-glucoside+malonyl-CoACHEBI:169949+coenzyme A(4-)
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:67348CC BY 4.0Reference data
apigenin 7-O-beta-D-glucoside+waterapigenin+beta-D-glucose
Catalysed by LCT
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:69679CC BY 4.0Reference data
Other names
2 names
Resolves to: apigenin 7-O-beta-D-glucoside
- Systematic name
- 7-(beta-D-glucopyranosyloxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-5-olate7-(β-D-glucopyranosyloxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-5-olate