acacetin-7-O-β-D-galactopyranoside
A glycosyloxyflavone that is the 7-O-β-D-galactopyranosyl derivative of acacetin. It is isolated from the flowering heads of Chrysanthemum morifolium and has been found to possess potent anti-HIV activity.
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 | C22H22O10 |
|---|---|
| Charge | 0 |
| Average mass | 446.408 Da |
| Monoisotopic mass | 446.1213 Da |
| Source | ChEBI |
| InChIKey | NLZCOTZRUWYPTP-WHCFWRGISA-N |
COc1ccc(-c2cc(=O)c3c(O)cc(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)cc3o2)cc1
InChI=1S/C22H22O10/c1-29-11-4-2-10(3-5-11)15-8-14(25)18-13(24)6-12(7-16(18)31-15)30-22-21(28)20(27)19(26)17(9-23)32-22/h2-8,17,19-24,26-28H,9H2,1H3/t17-,19+,20+,21-,22-/m1/s1
Also called
- 5-hydroxy-2-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl β-D-galactopyranoside
- 5,7-dihydroxy-4'-methoxyflavone-7-O-β-D-galactopyranoside
- 7-(β-D-galactopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
Cross-references
- reaxys:1359476
Activity roles
- anti-HIV agent
CHEBI:64946
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65361 |
acacetin-7-O-β-D-galactopyranoside | antibioticmech:chebi-0a135145b0 |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories