4-Aminobiphenyl (BioCAD00000004206)
{$topic}
Metabolite Card
Formula: C12H11N (169.0891)
SMILES: NC1=CC=C(C=C1)C1=CC=CC=C1
Synonyms [en]
4-aminobiphenyl; 4-biphenylamine; 4-Aminodiphenyl; p-Biphenylamine; Biphenyl-4-ylamine; Paraaminodiphenyl
Last reviewed on 2024-06-28.
Cite this Page
4-Aminobiphenyl. 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: BioCAD00000004206). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
4-Aminobiphenyl is an amine derivative of biphenyl. It is used to manufacture azo dyes. It is a known human carcinogen and so it has been largely replaced by less toxic compounds. It is similar to benzidine.
DBLinks
- CAS Registry Number: 92-67-1
- PubChem CID: 7102
- ChEBI: 1784
- HMDB: HMDB0013195
- LipidMaps:
- KEGG: C10998
- BioCyc:
- NCBI MeSH: 4-biphenylamine
- Wikipedia: 4-Aminobiphenyl
Other DBLinks
- CAS Registry Number: 116267-93-7
- CAS Registry Number: 2946-61-4
- CAS Registry Number: 92-67-1
- PubChem: 7102
- ChEBI: ChEBI:1784
- HMDB: HMDB0013195
- KEGG: C10998
- NCBI MeSH: 4-biphenylamine
- Wikipedia: 4-Aminobiphenyl
- RefMet: RM0020306
- MoNA: HMDB0013195_c_ms_100042
- MoNA: JP001641
- Metlin: METLIN_471
- Coconut NaturalProduct: CNP0049160.0
- Coconut NaturalProduct: CNP0320497.0
Class / Ontology
- WishartLab ClassyFire: [Biphenyls and derivatives] Biphenyls and derivatives
- RefMet: [Biphenyls] Biphenyls
- ChEBI: [CHEBI:1784] biphenyl-4-amine
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-211945 | Phase I - Functionalization of compounds |
| Reactome:R-BTA-211981 | Xenobiotics |
| Reactome:R-DRE-211897 | Cytochrome P450 - arranged by substrate type |
| Reactome:R-DRE-211957 | Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 |
| Reactome:R-HSA-211859 | Biological oxidations |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-211859 | Biological oxidations |
| Reactome:R-RNO-211945 | Phase I - Functionalization of compounds |
| Reactome:R-RNO-211981 | Xenobiotics |
| Reactome:R-SSC-211945 | Phase I - Functionalization of compounds |
| Reactome:R-SSC-211981 | Xenobiotics |
| Reactome:R-BTA-211859 | Biological oxidations |
| Reactome:R-DRE-211945 | Phase I - Functionalization of compounds |
| Reactome:R-DRE-211981 | Xenobiotics |
| Reactome:R-RNO-211859 | Biological oxidations |
| Reactome:R-SSC-1430728 | Metabolism |
| Reactome:R-SSC-211859 | Biological oxidations |
| Reactome:R-BTA-211897 | Cytochrome P450 - arranged by substrate type |
| Reactome:R-BTA-211957 | Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 |