apigenin 7-O-β-D-glucoside(1−)
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.).
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C21H19O10 |
|---|---|
| Charge | -1 |
| Average mass | 431.373 Da |
| Monoisotopic mass | 431.09837 Da |
| Source | ChEBI |
| InChIKey | KMOUJOKENFFTPU-QNDFHXLGSA-M |
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
InChI=1S/C21H20O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-7,16,18-24,26-28H,8H2/p-1/t16-,18-,19+,20-,21-/m1/s1
Also called
- 7-(β-D-glucopyranosyloxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-5-olate
- apigenin 7-O-β-D-glucoside
Activity roles
- antibacterial agent
CHEBI:33282
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:77722 |
apigenin 7-O-β-D-glucoside(1−) | antibioticmech:chebi-14d8f9c82d |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories