N-HYDROXY-2-AMINOFLUORENE

ONC1=CC2=C(C=C1)C3=C(C2)C=CC=C3

InChIKey=JJCLXJPUTJMRTM-UHFFFAOYSA-N

InChI=1S/C13H11NO/c15-14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8,14-15H,7H2

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Preferential carcinogen-DNA adduct formation at codons 12 and 14 in the human K-ras gene and their possible mechanisms.	2003 Aug 26	12924950
Prostate expression of N-acetyltransferase 1 (NAT1) and 2 (NAT2) in rapid and slow acetylator congenic Syrian hamster.	2003 Mar	12618593
Mass spectrometric investigation of the mechanism of inactivation of hamster arylamine N-acetyltransferase 1 by N-hydroxy-2-acetylaminofluorene.	2004 Mar	15025497
Aromatic amines in experimental cancer research: tissue-specific effects, an old problem and new solutions.	2007 Mar	17453932

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:52:41 GMT 2023` Edited by `admin` on `Fri Dec 15 18:52:41 GMT 2023`
Record UNII	61M94X4V24
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

N-HYDROXY-2-AMINOFLUORENE

Systematic Name

English

9H-FLUOREN-2-AMINE, N-HYDROXY-

Systematic Name

English

HYDROXY-2-AMINOFLUORENE, N-

Systematic Name

English

N-HYDROXY-2-FLUORENAMINE

Systematic Name

English

N-FLUORENE-2-YL-HYDROXYLAMINE [HSDB]

Common Name

English

N-2-FLUORENYLHYDROXYLAMINE

Systematic Name

English

HYDROXYLAMINE, N-FLUOREN-2-YL-

Systematic Name

English

2-(HYDROXYAMINO)FLUORENE

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID50201045