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Details

Stereochemistry ACHIRAL
Molecular Formula C16H9NO2
Molecular Weight 247.2482
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-NITROFLUORANTHENE

SMILES

[O-][N+](=O)C1=CC=C2C3=C(C=CC=C3)C4=C2C1=CC=C4

InChI

InChIKey=PIHGQKMEAMSUNA-UHFFFAOYSA-N
InChI=1S/C16H9NO2/c18-17(19)15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H

HIDE SMILES / InChI

Molecular Formula C16H9NO2
Molecular Weight 247.2482
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Multivariate QSAR study on the antimutagenic activity of flavonoids against 3-NFA on Salmonella typhimurium TA98.
2010-10
Differential effects of nitro-PAHs and amino-PAHs on cytokine and chemokine responses in human bronchial epithelial BEAS-2B cells.
2010-02-01
1-Nitropyrene stabilizes the mRNA of cytochrome P450 1a1, a carcinogen-metabolizing enzyme, via the Akt pathway.
2009-12
Signalling pathways involved in 1-nitropyrene (1-NP)-induced and 3-nitrofluoranthene (3-NF)-induced cell death in Hepa1c1c7 cells.
2009-11
3-nitrofluoranthene (3-NF)-induced apoptosis and programmed necrosis.
2009-07
3-Nitrofluoranthene (3-NF) but not 3-aminofluoranthene (3-AF) elicits apoptosis as well as programmed necrosis in Hepa1c1c7 cells.
2009-01-31
Absorption of nitro-polycyclic aromatic hydrocarbons by biomembrane models: effect of the medium lipophilicity.
2008-10
Singlet excited-state dynamics of nitropolycyclic aromatic hydrocarbons: direct measurements by femtosecond fluorescence up-conversion.
2007-02-01
Mutagenic activities and physicochemical properties of selected nitrobenzanthrones.
2006-11
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
A combined chemical and bioassay analysis of traffic-emitted polycyclic aromatic hydrocarbons.
2004-12-01
Derivatised carbon powder electrodes: reagentless pH sensors.
2004-07-08
Induction of CYP1A1, CYP1A2, and CYP1B1 mRNAs by nitropolycyclic aromatic hydrocarbons in various human tissue-derived cells: chemical-, cytochrome P450 isoform-, and cell-specific differences.
2002-06
Catechins are not major components responsible for anti-genotoxic effects of tea extracts against nitroarenes.
2001-09-20
Porphyrins with exocyclic rings. 16. Synthesis and spectroscopic characterization of fluoranthoporphyrins, a new class of highly conjugated porphyrin chromophores.
2001-05-04
Photodegradation of nitro-PAHs in viscous organic media used as models of organic aerosols.
2001-01-01
Bioactivation of diesel exhaust particle extracts and their major nitrated polycyclic aromatic hydrocarbon components, 1-nitropyrene and dinitropyrenes, by human cytochromes P450 1A1, 1A2, and 1B1.
2000-12-20
Nitration of carcinogenic and non-carcinogenic polycyclic aromatic hydrocarbons results in products able to induce transformation of Syrian hamster cells.
1983
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:46:45 GMT 2025
Edited
by admin
on Mon Mar 31 18:46:45 GMT 2025
Record UNII
R9796OQK2M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-NITROFLUORANTHENE
Systematic Name English
NSC-57468
Preferred Name English
4-NITROFLUORANTHENE
Systematic Name English
3-NITROFLUORANTHENE [IARC]
Common Name English
NITROFLUORANTHENE, 3-
Systematic Name English
FLUORANTHENE, 3-NITRO-
Systematic Name English
Code System Code Type Description
MESH
C033643
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
PRIMARY
NSC
57468
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
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EPA CompTox
DTXSID0074976
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
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FDA UNII
R9796OQK2M
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
PRIMARY
PUBCHEM
13462
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
PRIMARY
CAS
892-21-7
Created by admin on Mon Mar 31 18:46:45 GMT 2025 , Edited by admin on Mon Mar 31 18:46:45 GMT 2025
PRIMARY