dihydrooroxylin A
A dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 6. Isolated from Pisonia aculeata, it exhibits antitubercular 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 | C16H14O5 |
|---|---|
| Charge | 0 |
| Average mass | 286.283 Da |
| Monoisotopic mass | 286.08412 Da |
| Source | ChEBI |
| InChIKey | QUAPPCXFYKSDSV-UHFFFAOYSA-N |
COc1c(O)cc2c(c1O)C(=O)CC(c1ccccc1)O2
InChI=1S/C16H14O5/c1-20-16-11(18)8-13-14(15(16)19)10(17)7-12(21-13)9-5-3-2-4-6-9/h2-6,8,12,18-19H,7H2,1H3
Also called
- 5,7-dihydroxy-6-methoxy-2-phenyl-2,3-dihydro-4H-chromen-4-one
- 5,7-dihydroxy-6-methoxyflavanone
Cross-references
- hmdb:HMDB0037322
- lipidmaps:LMPK12140611
- reaxys:294379
Activity roles
- antitubercular agent
CHEBI:33231
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:67376 |
dihydrooroxylin A | antibioticmech:chebi-5411e5d51e |
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