exiguaflavanone A
A tetrahydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5, 7, 2' and 6' and a lavandulyl group at position 8. Isolated from Sophora exigua and Artemisia indica, it exhibits antimalarial 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 | C25H28O6 |
|---|---|
| Charge | 0 |
| Average mass | 424.493 Da |
| Monoisotopic mass | 424.18859 Da |
| Source | ChEBI |
| InChIKey | FPUREMWTZVLZBZ-QRQCRPRQSA-N |
[H][C@@]1(c2c(O)cccc2O)CC(=O)c2c(O)cc(O)c(C[C@@H](CC=C(C)C)C(=C)C)c2O1
InChI=1S/C25H28O6/c1-13(2)8-9-15(14(3)4)10-16-19(28)11-20(29)24-21(30)12-22(31-25(16)24)23-17(26)6-5-7-18(23)27/h5-8,11,15,22,26-29H,3,9-10,12H2,1-2,4H3/t15-,22+/m1/s1
Also called
- (2S)-2-(2,6-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2,3-dihydro-4H-chromen-4-one
Cross-references
- lipidmaps:LMPK12140111
- reaxys:5362663
Activity roles
- antimalarial
CHEBI:38068
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65891 |
exiguaflavanone A | antibioticmech:chebi-b5bcf06dd9 |
2026-08-30 |
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories