deoxyviolacein
A member of the class of oxindoles resulting from formal oxidative coupling between the 3-position of 1,3-dihydro-2H-indol-2-one and the 3-position of 1,3-dihydro-2H-pyrrol-2-one, which is substituted at the 5 position by a 1H-indol-3-yl group, where the newly-formed double bond has E configuration.
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 | C20H13N3O2 |
|---|---|
| Charge | 0 |
| Average mass | 327.343 Da |
| Monoisotopic mass | 327.10078 Da |
| Source | ChEBI |
| InChIKey | OJUJNNKCVPCATE-QGOAFFKASA-N |
O=C1NC(c2cnc3ccccc23)=C/C1=C1\C(=O)Nc2ccccc21
InChI=1S/C20H13N3O2/c24-19-13(18-12-6-2-4-8-16(12)22-20(18)25)9-17(23-19)14-10-21-15-7-3-1-5-11(14)15/h1-10,21H,(H,22,25)(H,23,24)/b18-13+
Also called
- (3E)-3-[5-(1H-indol-3-yl)-2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene]-1,3-dihydro-2H-indol-2-one
Cross-references
- kegg.compound:C21133
- metacyc.compound:CPD-14318
- reaxys:10779335
Patents and articles
Activity roles
- antibacterial agent
CHEBI:33282 - antifungal agent
CHEBI:35718
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:131915 |
deoxyviolacein | antibioticmech:chebi-038273f766 |
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
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories