licorisoflavan A
A member of the class of hydroxyisoflavans that is the 7-O-methyl derivative of licoricidin. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial 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 | C27H34O5 |
|---|---|
| Charge | 0 |
| Average mass | 438.564 Da |
| Monoisotopic mass | 438.24062 Da |
| Source | ChEBI |
| InChIKey | GDAAEAXMNLVRCZ-SFHVURJKSA-N |
[H][C@@]1(c2ccc(O)c(CC=C(C)C)c2O)COc2cc(OC)c(CC=C(C)C)c(OC)c2C1
InChI=1S/C27H34O5/c1-16(2)7-9-20-23(28)12-11-19(26(20)29)18-13-22-25(32-15-18)14-24(30-5)21(27(22)31-6)10-8-17(3)4/h7-8,11-12,14,18,28-29H,9-10,13,15H2,1-6H3/t18-/m0/s1
Also called
- 4-[(3R)-5,7-dimethoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol
- (+)-2',4'-dihydroxy-5,7-dimethoxy-6,3'-diprenylisoflavan
- 5-O-methyllicoricidin
- 7-O-methyllicoricidin
Cross-references
- cas:129314-37-0
- hmdb:HMDB0034184
- lipidmaps:LMPK12080046
- reaxys:5461708
Activity roles
- antibacterial agent
CHEBI:33282
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:69083 |
licorisoflavan A | antibioticmech:chebi-aab8f4637a |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories