erylatissin A
A member of the class of 7-hydroxyisoflavones in which isoflavone is substituted by hydroxy groups at the 7 and 3' positions, a methoxy group at the 4' position and a prenyl group at position 5'. Isolated from the stem wood of Erythrina latissima, it exhibits antimicrobial and radical scavenging activities.
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 | C21H20O5 |
|---|---|
| Charge | 0 |
| Average mass | 352.386 Da |
| Monoisotopic mass | 352.13107 Da |
| Source | ChEBI |
| InChIKey | CEXYMYPXHMUTTJ-UHFFFAOYSA-N |
COc1c(O)cc(-c2coc3cc(O)ccc3c2=O)cc1CC=C(C)C
InChI=1S/C21H20O5/c1-12(2)4-5-13-8-14(9-18(23)21(13)25-3)17-11-26-19-10-15(22)6-7-16(19)20(17)24/h4,6-11,22-23H,5H2,1-3H3
Also called
- 7-hydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-4H-chromen-4-one
- 7,3'-dihydroxy-4'-methoxy-5'-(γ,γ-dimethylallyl)isoflavone
Cross-references
- reaxys:10587410
Activity roles
- antimicrobial agent
CHEBI:33281
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65863 |
erylatissin A | antibioticmech:chebi-db2dfa5226 |
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