CHEBI:1784 - biphenyl-4-amine

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ChEBI Name biphenyl-4-amine
Definition An aminobiphenyl that is biphenyl substituted by an amino group at position 4.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C12H11N
Net Charge 0
Average Mass 169.22248
Monoisotopic Mass 169.08915
InChI InChI=1S/C12H11N/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,13H2
SMILES Nc1ccc(cc1)-c1ccccc1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): 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.
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ChEBI Ontology
Outgoing biphenyl-4-amine (CHEBI:1784) has parent hydride biphenyl (CHEBI:17097)
biphenyl-4-amine (CHEBI:1784) has role carcinogenic agent (CHEBI:50903)
biphenyl-4-amine (CHEBI:1784) is a aminobiphenyl (CHEBI:22496)
Incoming 4'-aminobiphenyl-4-ol (CHEBI:35435) has functional parent biphenyl-4-amine (CHEBI:1784)
N-acetoxy-1,1'-biphenyl-4-amine (CHEBI:16395) has functional parent biphenyl-4-amine (CHEBI:1784)
N-hydroxy-4-acetylaminobiphenyl (CHEBI:16434) has functional parent biphenyl-4-amine (CHEBI:1784)
N-hydroxy-4-aminobiphenyl (CHEBI:16580) has functional parent biphenyl-4-amine (CHEBI:1784)
N-hydroxy-4-aminobiphenyl O-glucuronide (CHEBI:32649) has functional parent biphenyl-4-amine (CHEBI:1784)
N-hydroxy-4-aminobiphenyl O-sulfate (CHEBI:32701) has functional parent biphenyl-4-amine (CHEBI:1784)
Synonyms Sources
4-amino-1,1'-biphenyl ChemIDplus
4-Aminobiphenyl KEGG COMPOUND
4-aminodiphenyl ChemIDplus
4-biphenylamine ChemIDplus
biphenyl-4-ylamine NIST Chemistry WebBook
p-aminodiphenyl NIST Chemistry WebBook
p-biphenylamine ChemIDplus
p-phenylaniline NIST Chemistry WebBook
p-xenylamine ChemIDplus
paraaminodiphenyl NIST Chemistry WebBook
Manual Xrefs Databases
4-Aminobiphenyl Wikipedia
HMDB0013195 HMDB
View more database links
Registry Numbers Types Sources
365629 Gmelin Registry Number Gmelin
386533 Reaxys Registry Number Reaxys
386533 Beilstein Registry Number Beilstein
92-67-1 CAS Registry Number ChemIDplus
92-67-1 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
12778203 PubMed citation Europe PMC
15880493 PubMed citation Europe PMC
20433335 PubMed citation Europe PMC
841184 PubMed citation Europe PMC
8847111 PubMed citation Europe PMC
Last Modified
08 May 2014