(+)-trans-fustin
The (2R,3R)-stereoisomer of fustin.
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
- fustin
CHEBI:5202
Chemical structure
| Molecular formula | C15H12O6 |
|---|---|
| Charge | 0 |
| Average mass | 288.255 Da |
| Monoisotopic mass | 288.06339 Da |
| Source | ChEBI |
| InChIKey | FNUPUYFWZXZMIE-LSDHHAIUSA-N |
O=C1c2ccc(O)cc2O[C@H](c2ccc(O)c(O)c2)[C@H]1O
InChI=1S/C15H12O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,14-18,20H/t14-,15+/m0/s1
Also called
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-chromen-4-one
- (+)-2,3-dihydrofisetin
- (+)-3,3',4',7-tetrahydroxyflavanone
- (+)-fustin
- (2R,3R)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4H-1-benzopyran-4-one
- (2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-4-one
- (2R,3R)-3,7,3',4'-tetrahydroxyflavanone
- (2R,3R)-fustin
- (2R-trans)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-4H-1-benzopyran-4-one
- fustin (2R,3R)-form
Cross-references
Activity roles
- antiviral agent
CHEBI:22587
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:228234 |
(+)-trans-fustin | antibioticmech:chebi-c713067564 |
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