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| Formula | C9H6N2O3 |
| Net Charge | 0 |
| Average Mass | 190.158 |
| Monoisotopic Mass | 190.03784 |
| SMILES | O=[N+]([O-])c1cc[n+]([O-])c2ccccc12 |
| InChI | InChI=1S/C9H6N2O3/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6H |
| InChIKey | YHQDZJICGQWFHK-UHFFFAOYSA-N |
| Wikipedia |
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| Roles Classification |
|---|
| Biological Role: | carcinogenic agent A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 4-nitroquinoline N-oxide (CHEBI:16907) has role carcinogenic agent (CHEBI:50903) |
| 4-nitroquinoline N-oxide (CHEBI:16907) is a C-nitro compound (CHEBI:35716) |
| 4-nitroquinoline N-oxide (CHEBI:16907) is a quinoline N-oxide (CHEBI:26508) |
| IUPAC Name |
|---|
| 4-nitroquinoline 1-oxide |
| Synonyms | Source |
|---|---|
| 4-Nitroquinoline N-oxide | KEGG COMPOUND |
| 4-Nitroquinoline 1-oxide | KEGG COMPOUND |
| 4-nitroquinoline N-oxide | ChEBI |
| 4-nitroquinoline 1-oxide | ChEBI |
| 4-Nitroquinoline-1-oxide | ChemIDplus |
| 4-Nitroquinoline-N-oxide | ChemIDplus |
| UniProt Name | Source |
|---|---|
| 4-nitroquinoline N-oxide | UniProt |
| Manual Xrefs | Databases |
|---|---|
| C03474 | KEGG COMPOUND |
| C03474 | KEGG COMPOUND |
| 4-Nitroquinoline_1-oxide | Wikipedia |
| Registry Numbers | Sources |
|---|---|
| Reaxys:165756 | Reaxys |
| CAS:56-57-5 | KEGG COMPOUND |
| CAS:56-57-5 | NIST Chemistry WebBook |
| Citations |
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