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CHEBI:32211 - tetrangomycin
| Formula | C19H14O5 |
| Net Charge | 0 |
| Average Mass | 322.316 |
| Monoisotopic Mass | 322.08412 |
| SMILES | C[C@]1(O)CC(=O)c2c(ccc3c2C(=O)c2cccc(O)c2C3=O)C1 |
| InChI | InChI=1S/C19H14O5/c1-19(24)7-9-5-6-11-16(14(9)13(21)8-19)18(23)10-3-2-4-12(20)15(10)17(11)22/h2-6,20,24H,7-8H2,1H3/t19-/m1/s1 |
| InChIKey | UGEKKXLEYACFTD-LJQANCHMSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Streptomyces cyanogenus (ncbitaxon:80860) | - | PubMed (21188999) | Ethyl acetate extract of broth Strain: S 136 |
| Roles Classification |
|---|
| Biological Roles: | antimicrobial agent A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans. bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| tetrangomycin (CHEBI:32211) is a angucycline antibiotic (CHEBI:70737) |
| tetrangomycin (CHEBI:32211) is a cyclic ketone (CHEBI:3992) |
| tetrangomycin (CHEBI:32211) is a phenols (CHEBI:33853) |
| tetrangomycin (CHEBI:32211) is a tertiary alcohol (CHEBI:26878) |
| Incoming Relation(s) |
| moromycin A (CHEBI:66403) has functional parent tetrangomycin (CHEBI:32211) |
| moromycin B (CHEBI:66404) has functional parent tetrangomycin (CHEBI:32211) |
| IUPAC Name |
|---|
| (3R)-3,8-dihydroxy-3-methyl-3,4-dihydrotetraphene-1,7,12(2H)-trione |
| Synonyms | Source |
|---|---|
| Tetrangomycin | KEGG COMPOUND |
| (−)-tetrangomycin | ChEBI |
| (+)-3,4-dihydro-3,8-dihydroxy-3-methylbenz(a)anthracene- 1,7,12(2H)-trione | ChemIDplus |
| Citations |
|---|