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Details

Stereochemistry ACHIRAL
Molecular Formula C14H15NO
Molecular Weight 213.275
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-HYDROXY-3,2'-DIMETHYL-4-AMINOBIPHENYL

SMILES

CC1=CC=CC=C1C2=CC=C(NO)C(C)=C2

InChI

InChIKey=UTWFEHCOAXSLRA-UHFFFAOYSA-N
InChI=1S/C14H15NO/c1-10-5-3-4-6-13(10)12-7-8-14(15-16)11(2)9-12/h3-9,15-16H,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H15NO
Molecular Weight 213.275
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Carcinogenicity of the N-hydroxy derivative of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine, 2-amino-3, 8-dimethyl-imidazo[4,5-f]quinoxaline and 3, 2'-dimethyl-4-aminobiphenyl in the rat.
2000-07-03
Dose dependence of N-hydroxy-3,2'-dimethyl-4-aminobiphenyl-induced rat prostate carcinogenesis.
1992-07
Preparation and characterization of antibodies against 3,2'-dimethyl-4-aminobiphenyl-modified DNA.
1989-08
Polymorphic expression of acetyl coenzyme A-dependent arylamine N-acetyltransferase and acetyl coenzyme A-dependent O-acetyltransferase-mediated activation of N-hydroxyarylamines by human bladder cytosol.
1989-05-01
Metabolism of aromatic amines: relationships of N-acetylation, O-acetylation, N,O-acetyltransfer and deacetylation in human liver and urinary bladder.
1989-04
Induction of repair synthesis of DNA in mammary and urinary bladder epithelial cells by N-hydroxy derivatives of carcinogenic arylamines.
1988-08-01
Acetylator genotype-dependent metabolic activation of carcinogenic N-hydroxyarylamines by S-acetyl coenzyme A-dependent enzymes of inbred hamster tissue cytosols: relationship to arylamine N-acetyltransferase.
1987-12
Acetyl coenzyme A-dependent metabolic activation of N-hydroxy-3,2'-dimethyl-4-aminobiphenyl and several carcinogenic N-hydroxy arylamines in relation to tissue and species differences, other acyl donors, and arylhydroxamic acid-dependent acyltransferases.
1986-06
DNA adducts formed from the probable proximate carcinogen, N-hydroxy-3,2' -dimethyl-4-aminobiphenyl, by acid catalysis or S-acetyl coenzyme A-dependent enzymatic esterification.
1985-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:48:51 GMT 2025
Edited
by admin
on Mon Mar 31 21:48:51 GMT 2025
Record UNII
AI7FN5EVN2
Record Status Validated (UNII)
Record Version
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Name Type Language
N-HYDROXY-3,2'-DIMETHYL-4-AMINOBIPHENYL
Systematic Name English
(1,1'-BIPHENYL)-4-AMINE, 2',3-DIMETHYL-N-HYDROXY-
Preferred Name English
Code System Code Type Description
FDA UNII
AI7FN5EVN2
Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025
PRIMARY
CAS
70786-72-0
Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025
PRIMARY
PUBCHEM
108211
Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID50221046
Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025
PRIMARY