2-NITROSOFLUORENE

O=NC1=CC=C2C(CC3=CC=CC=C23)=C1

InChIKey=XZWGJDANCSXBDW-UHFFFAOYSA-N

InChI=1S/C13H9NO/c15-14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7H2

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

PubMed

Title	Date	PubMed
Cadmium alters the biotransformation of carcinogenic aromatic amines by arylamine N-acetyltransferase xenobiotic-metabolizing enzymes: molecular, cellular, and in vivo studies.	2010-12	20810355
Isoform-selective inactivation of human arylamine N-acetyltransferases by reactive metabolites of carcinogenic arylamines.	2009-12	19842618
Human arylamine N-acetyltransferase 1: in vitro and intracellular inactivation by nitrosoarene metabolites of toxic and carcinogenic arylamines.	2008-10	18759501
Aromatic amines in experimental cancer research: tissue-specific effects, an old problem and new solutions.	2007-03	17453932
Mass spectrometric investigation of the mechanism of inactivation of hamster arylamine N-acetyltransferase 1 by N-hydroxy-2-acetylaminofluorene.	2004-03	15025497

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:40:26 GMT 2025` Edited by `admin` on `Mon Mar 31 19:40:26 GMT 2025`
Record UNII	34E9V9B29K
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

2-NITROSOFLUORENE

Systematic Name

English

2-NITROSOFLUORENE [HSDB]

Preferred Name

English

9H-FLUORENE, 2-NITROSO-

Systematic Name

English

NITROSOFLUORENE, 2-

Systematic Name

English

FLUORENE, 2-NITROSO-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID2075211