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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO3
Molecular Weight 153.1354
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-NITROANISOLE

SMILES

COC1=CC=CC=C1[N+]([O-])=O

InChI

InChIKey=CFBYEGUGFPZCNF-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7NO3
Molecular Weight 153.1354
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Early Detection of Genotoxic Urinary Bladder Carcinogens by Immunohistochemistry for γ-H2AX.
2015-12
Identification of rat cytochromes P450 metabolizing N-(2-methoxyphenyl)hydroxylamine, a human metabolite of the environmental pollutants and carcinogens o-anisidine and o-nitroanisole.
2010
Genotoxic mechanisms for the carcinogenicity of the environmental pollutants and carcinogens o-anisidine and 2-nitroanisole follow from adducts generated by their metabolite N-(2-methoxyphenyl)-hydroxylamine with deoxyguanosine in DNA.
2009-03
Rat cytochromes P450 oxidize 2-nitrophenol, a human metabolite of carcinogenic 2-nitroanisole.
2009
Cytochrome P450-mediated metabolism of N-(2-methoxyphenyl)-hydroxylamine, a human metabolite of the environmental pollutants and carcinogens o-anisidine and o-nitroanisole.
2008-12
Oxidation of carcinogenic 2-nitroanisole by rat cytochromes P450 - similarity between human and rat enzymes.
2008-09
Structure and performance of silica-based monolithic HPLC columns.
2008-08
In vivo Comet assay on isolated kidney cells to distinguish genotoxic carcinogens from epigenetic carcinogens or cytotoxic compounds.
2007-06-15
Tumorigenic potential and the molecular mechanism of the carcinogenic effect exerted by 2-nitroanisole.
2007-01-05
Oxidative detoxication of carcinogenic 2-nitroanisole by human, rat and rabbit cytochrome P450.
2006-12
Carcinogenic pollutants o-nitroanisole and o-anisidine are substrates and inducers of cytochromes P450.
2005-12
Association of liver hemangiosarcoma and secondary iron overload in B6C3F1 mice--the National Toxicology Program experience.
2004-06-18
Enzymes involved in the metabolism of the carcinogen 2-nitroanisole: evidence for its oxidative detoxication by human cytochromes P450.
2004-05
Identification of a genotoxic mechanism for 2-nitroanisole carcinogenicity and of its carcinogenic potential for humans.
2004-05
o-Nitroanisole.
2004
3-pyrrolines are mechanism-based inactivators of the quinone-dependent amine oxidases but only substrates of the flavin-dependent amine oxidases.
2002-10-16
o-Nitroanisole.
2002
Transcriptional activation of stress genes and cytotoxicity in human liver carcinoma cells (HepG2) exposed to 2,4,6-trinitrotoluene, 2,4-dinitrotoluene, and 2,6-dinitrotoluene.
2001-06
Synthesis and antibacterial activity of 5-nitrofuryl and 3-methoxy-2-nitrophenyl derivatives of 6 beta-aminopenicillanic, 7 beta-aminocephalosporanic and 7 beta-aminodesacetoxy-cephalosporanic acids.
2001
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:46:18 GMT 2025
Edited
by admin
on Mon Mar 31 18:46:18 GMT 2025
Record UNII
ZRE7HLZ17K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-NITROANISOLE
HSDB  
Preferred Name English
O-NITROANISOLE
MI  
Common Name English
NSC-5506
Code English
2-METHOXYNITROBENZENE
Systematic Name English
NITROANISOLE, O-
Common Name English
O-NITROBENZENE METHYL ETHER
Common Name English
2-METHOXY-1-NITROBENZENE
Systematic Name English
ANISOLE, O-NITRO-
Common Name English
1-METHOXY-2-NITROBENZENE
Systematic Name English
O-NITROANISOLE [MI]
Common Name English
2-NITROANISOLE [HSDB]
Common Name English
O-METHOXYNITROBENZENE
Common Name English
O-NITROPHENYL METHYL ETHER
Common Name English
1-NITRO-2-METHOXYBENZENE
Systematic Name English
2-NITROANISOLE [IARC]
Common Name English
2-NITROMETHOXYBENZENE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C45179
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
Code System Code Type Description
FDA UNII
ZRE7HLZ17K
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
WIKIPEDIA
o-Nitroanisole
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
NSC
5506
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
MESH
C005328
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
HSDB
5186
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
SMS_ID
300000053549
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-052-1
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
CHEBI
48722
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
NCI_THESAURUS
C44312
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY NCIT
CAS
91-23-6
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
PUBCHEM
7048
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY
MERCK INDEX
m7941
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID3020962
Created by admin on Mon Mar 31 18:46:18 GMT 2025 , Edited by admin on Mon Mar 31 18:46:18 GMT 2025
PRIMARY