asperlactone
A member of the class of butenolides that is furan-2(5H)-one substituted by (2S,3S)-3-methyloxiran-2-yl and (1S)-1-hydroxyethyl group at positions 3 and 5R, respectively. It is a secondary metabolite isolated from Aspergillus ochraceus that exhibits antifungal and antibacterial properties.
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
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CHEBI:26188 -
CHEBI:32955 -
CHEBI:35681 -
CHEBI:50523 - antibiotic antifungal agent
CHEBI:86478
Chemical structure
| Molecular formula | C9H12O4 |
|---|---|
| Charge | 0 |
| Average mass | 184.191 Da |
| Monoisotopic mass | 184.07356 Da |
| Source | ChEBI |
| InChIKey | VMLNPJDEXLLCQG-DGCAKLBHSA-N |
[H][C@]1([C@H](C)O)C=C([C@@H]2O[C@H]2C)C(=O)O1
InChI=1S/C9H12O4/c1-4(10)7-3-6(9(11)13-7)8-5(2)12-8/h3-5,7-8,10H,1-2H3/t4-,5-,7+,8+/m0/s1
Also called
- (5R)-5-[(1S)-1-hydroxyethyl]-3-[(2S,3S)-3-methyloxiran-2-yl]furan-2(5H)-one
- 5R-[(1S)-1-hydroxyethyl]-3-[(2S,3S)-3-methyl-2-oxiranyl]-2(5H)-furanone
Cross-references
Activity roles
- antibacterial agent
CHEBI:33282 - antifungal agent
CHEBI:35718
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:156386 |
asperlactone | antibioticmech:chebi-40deacf6c8 |
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