1-Nitronaphthalene-5,6-oxide (BioCAD00000001420)
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Metabolite Card
Formula: C10H7NO3 (189.0426)
SMILES: O=N(=O)C1=CC=CC2=C1C=CC1OC21
Synonyms [en]
1-Nitronaphthalene-5,6-oxide; 7bH-naphtho1; 2-boxirene; Q27115813; 4-nitro-1aH; DTXSID601343586
Last reviewed on 2024-06-28.
Cite this Page
1-Nitronaphthalene-5,6-oxide. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000001420). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
This compound belongs to the family of Nitronaphthalenes. These are polycyclic aromatic compounds containing a naphthalene moiety substituted by one or more nitro groups.
DBLinks
- CAS Registry Number:
- PubChem CID: 11954051
- ChEBI: 34105
- HMDB: HMDB0060331
- LipidMaps:
- KEGG: C14800
- BioCyc:
- NCBI MeSH:
- Wikipedia:
Other DBLinks
- PubChem: 11954051
- ChEBI: ChEBI:34105
- HMDB: HMDB0060331
- KEGG: C14800
- Metlin: METLIN_70332
- Coconut NaturalProduct: CNP0604918.0
Class / Ontology
- WishartLab ClassyFire: [Nitronaphthalenes] Nitronaphthalenes
- ChEBI: [CHEBI:34105] 1-Nitronaphthalene-5,6-oxide
| ID | EC Number | Name |
|---|---|---|
| KEGG:R07022 | 1.14.14.1 | 1-nitronaphthalene,NADPH:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing) |
| KEGG:R07025 | 2.5.1.18 | 1-nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene glutathione-lyase (epoxide-forming) |
| KEGG:R07026 | 2.5.1.18 | 1-nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene glutathione-lyase (epoxide-forming) |
| KEGG:R07027 | 3.3.2.9 | 1-nitronaphthalene-5,6-oxide hydrolase |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| PathBank:SMP0001941 | Glutathione Metabolism II |
| PathBank:SMP0122133 | Glutathione Metabolism II |