Page last updated: 2024-12-05

1-nitronaphthalene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

## 1-Nitronaphthalene: A Versatile Molecule for Research

1-Nitronaphthalene is an organic compound with the molecular formula C₁₀H₇NO₂. It's a yellow solid at room temperature and is commonly used in various research fields due to its unique properties:

**Structure and Properties:**

* It has a planar, aromatic structure with a nitro group (-NO₂) attached to the first carbon atom of the naphthalene ring.
* It exhibits high thermal stability and is relatively non-reactive under normal conditions.
* It absorbs strongly in the UV-Vis region, making it suitable for various spectroscopic studies.
* It is fluorescent and can be used in fluorescence microscopy and other imaging techniques.

**Applications in Research:**

1. **Organic Synthesis:** 1-Nitronaphthalene serves as a building block for synthesizing various complex organic compounds, including pharmaceuticals, dyes, and polymers. Its nitro group can be easily reduced to an amine group, providing a versatile functional group for further reactions.

2. **Materials Science:** 1-Nitronaphthalene is a good candidate for organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Its high thermal stability and electronic properties make it suitable for these applications.

3. **Analytical Chemistry:** 1-Nitronaphthalene is used as a standard in analytical chemistry for calibration and validation of various analytical methods. Its distinct fluorescence properties make it useful for fluorescence spectroscopy and chromatography.

4. **Biomedical Research:** 1-Nitronaphthalene exhibits anti-inflammatory and analgesic properties, making it a potential target for the development of novel drugs. Its fluorescent properties are also valuable for imaging and tracking biological processes.

5. **Environmental Science:** 1-Nitronaphthalene is a potential environmental pollutant, as it is produced during the combustion of fossil fuels. Studying its environmental fate and transport is important for understanding its potential impact on ecosystems.

**Importance for Research:**

1-Nitronaphthalene is an important research tool due to its versatility and unique properties. Its use in organic synthesis, materials science, analytical chemistry, biomedical research, and environmental science highlights its diverse applications. Further research on 1-nitronaphthalene can lead to the development of novel materials, technologies, and therapeutic agents.

1-nitronaphthalene: RN given refers to cpd with locant for nitro moiety in 1 position [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-nitronaphthalene : A mononitronaphthalene substituted by a nitro group at position 1. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

mononitronaphthalene : A nitronaphthalene carrying a single nitro group at unspecified position. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

nitronaphthalene : A nitroarene that is naphthalene substituted by at least one nitro group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID6849
CHEMBL ID165373
CHEBI ID34104
SCHEMBL ID57184
MeSH IDM0066744

Synonyms (73)

Synonym
un2538
naphthalene, nitro-
naphthalene, mononitro-
mononitronaphthalene
wln: l66j bnw
.alpha.-nitronaphthalene
nitrol (pesticide)
nsc-9584
naphthalene, 1-nitro-
nci-c01956
86-57-7
nitrol
1-nitronaphthalene
nsc9584
inchi=1/c10h7no2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7
NCGC00091715-01
alpha-nitronaphthalene
1-nitronaphthaline
nitrol (van)
hsdb 2887
naphthalene, alpha-nitro-
einecs 201-684-5
ai3-00477
1-nitronaftalen [czech]
brn 1867714
nsc 9584
ccris 450
1-nitronaphthalene, 99%
NCGC00091715-02
CHEBI:34104 ,
1-nitro-naphthalene
CHEMBL165373 ,
N0212
bdbm50282618
AKOS000120000
1-nitro-4-phenylbenzene;4-nitro-1-biphenyl;4-nitro-bipheny
A24106
NCGC00091715-03
dtxsid7020978 ,
cas-86-57-7
NCGC00256373-01
dtxcid70978
tox21_302759
tox21_201407
NCGC00258958-01
27254-36-0
nitronaphthalene [un2538] [flammable solid]
nitronaphthalene
FT-0641778
a51np1dl2t ,
unii-a51np1dl2t
1-nitronaftalen
FT-0608156
AE-562/40180003
nitronaphthalene, 1-
1-nitronaphthalene [mi]
1-nitronaphthalene [hsdb]
1-nitronaphthalene [iarc]
SCHEMBL57184
1-nitronapthalene
nitro-naphthalene
alpha-nitro-naphthalene
STR03423
AC-29181
mfcd00003913
1-nitronaphthalene, bcr(r) certified reference material
1-nitronaphthalene, purum, >=98.0% (gc)
1-nitronaphthalene 10 microg/ml in cyclohexane
nitronaphthalin
Q14848739
EN300-19781
D97666
|a-nitronaphthalene

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The most toxic was 1-nitronaphthalene with no mice surviving doses greater than 1 mmol kg-1."( Comparative cytotoxicity of naphthalene and its monomethyl- and mononitro-derivatives in the mouse lung.
Dearden, LC; Do, DH; Kim, TS; Rasmussen, RE, 1986
)
0.59
" Pretreatment with Aroclor 1254 or beta-naphthoflavone (beta-NF) did not alter the LD50 of 1-NN."( 1-Nitronaphthalene toxicity in rat lung and liver: effects of inhibiting and inducing cytochrome P450 activity.
Carthew, P; Dinsdale, D; Verschoyle, RD; Wolf, CR, 1993
)
1.73
" From these experiments, we conclude that retinol pretreatment decreases the severity of 2-nitronaphthalene and paraquat-induced pulmonary toxicity, apparently by inhibiting the inflammatory responses associated with the progression of toxic injury."( Modulation of chemical-induced lung and liver toxicity by all-trans-retinol in the male Sprague-Dawley rat.
Sauer, JM; Sipes, IG, 1995
)
0.29

Dosage Studied

ExcerptRelevanceReference
" This study examined the dose-response and durational effects of m-xylene inhalation on cytochrome P-450 activities in the respiratory tract and liver as well as the effects of these CYP450 alterations on 1-nitronaphthalene (1-NN)-induced respiratory or hepatic toxicity."( Inhibition of rat respiratory-tract cytochrome P-450 activity after acute low-level m-xylene inhalation: role in 1-nitronaphthalene toxicity.
Foy, JW; Schatz, RA, 2004
)
0.72
" BALF and lung tissue were obtained 24 h after dosing from these animals and matched control rats post-mortem."( Characterization of the biochemical effects of 1-nitronaphthalene in rats using global metabolic profiling by NMR spectroscopy and pattern recognition.
Azmi, J; Connelly, J; Griffin, JL; Holmes, E; Nicholson, JK; Shore, RF,
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
mononitronaphthaleneA nitronaphthalene carrying a single nitro group at unspecified position.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (7)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency89.43130.007215.758889.3584AID1224835
GLI family zinc finger 3Homo sapiens (human)Potency0.24340.000714.592883.7951AID1259369
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency44.66840.011212.4002100.0000AID1030
estrogen nuclear receptor alphaHomo sapiens (human)Potency0.12310.000229.305416,493.5996AID743075
aryl hydrocarbon receptorHomo sapiens (human)Potency30.84110.000723.06741,258.9301AID743085; AID743122
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency53.87190.000627.21521,122.0200AID651741; AID743202; AID743219
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (15)

Processvia Protein(s)Taxonomy
regulation of autophagyHistone acetyltransferase KAT8Homo sapiens (human)
negative regulation of epithelial to mesenchymal transitionHistone acetyltransferase KAT8Homo sapiens (human)
neurogenesisHistone acetyltransferase KAT8Homo sapiens (human)
myeloid cell differentiationHistone acetyltransferase KAT8Homo sapiens (human)
negative regulation of type I interferon productionHistone acetyltransferase KAT8Homo sapiens (human)
post-embryonic hemopoiesisHistone acetyltransferase KAT8Homo sapiens (human)
transcription initiation-coupled chromatin remodelingHistone acetyltransferase KAT8Homo sapiens (human)
negative regulation of DNA-templated transcriptionHistone acetyltransferase KAT8Homo sapiens (human)
positive regulation of DNA-templated transcriptionHistone acetyltransferase KAT8Homo sapiens (human)
oogenesisHistone acetyltransferase KAT8Homo sapiens (human)
regulation of mRNA processingHistone acetyltransferase KAT8Homo sapiens (human)
positive regulation of transcription initiation by RNA polymerase IIHistone acetyltransferase KAT8Homo sapiens (human)
positive regulation of skeletal muscle satellite cell differentiationHistone acetyltransferase KAT8Homo sapiens (human)
regulation of mitochondrial transcriptionHistone acetyltransferase KAT8Homo sapiens (human)
regulation of transcription by RNA polymerase IIHistone acetyltransferase KAT8Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (13)

Processvia Protein(s)Taxonomy
histone H4K5 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
histone H4K8 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
histone H4K16 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
transcription coactivator activityHistone acetyltransferase KAT8Homo sapiens (human)
protein bindingHistone acetyltransferase KAT8Homo sapiens (human)
histone H4 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
enzyme bindingHistone acetyltransferase KAT8Homo sapiens (human)
histone H4K5 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
histone H4K8 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
metal ion bindingHistone acetyltransferase KAT8Homo sapiens (human)
histone H4K16 acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingHistone acetyltransferase KAT8Homo sapiens (human)
peptide-lysine-N-acetyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
protein propionyltransferase activityHistone acetyltransferase KAT8Homo sapiens (human)
transcription coregulator activityHistone acetyltransferase KAT8Homo sapiens (human)
chromatin bindingHistone acetyltransferase KAT8Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (12)

Processvia Protein(s)Taxonomy
nucleusHistone acetyltransferase KAT8Homo sapiens (human)
chromosomeHistone acetyltransferase KAT8Homo sapiens (human)
kinetochoreHistone acetyltransferase KAT8Homo sapiens (human)
nucleusHistone acetyltransferase KAT8Homo sapiens (human)
nucleoplasmHistone acetyltransferase KAT8Homo sapiens (human)
mitochondrionHistone acetyltransferase KAT8Homo sapiens (human)
nuclear matrixHistone acetyltransferase KAT8Homo sapiens (human)
NSL complexHistone acetyltransferase KAT8Homo sapiens (human)
MSL complexHistone acetyltransferase KAT8Homo sapiens (human)
histone acetyltransferase complexHistone acetyltransferase KAT8Homo sapiens (human)
MLL1 complexHistone acetyltransferase KAT8Homo sapiens (human)
chromatinHistone acetyltransferase KAT8Homo sapiens (human)
NuA4 histone acetyltransferase complexHistone acetyltransferase KAT8Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1507709Inhibition of N-terminal His6-tagged KAT8 catalytic domain (125 to 458 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) using SGRGKGGKGLGKGGAKRHRK-NH2 as substrate after 5 mins in presence of Ac-CoA by fluorescence assay2017European journal of medicinal chemistry, Aug-18, Volume: 136The relevance of K
AID200690Mutagenic activity in an Ames test on Salmonella Typhimurium TA98; Activity is log of revertants/nmol1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Structure-activity relationship of mutagenic aromatic and heteroaromatic nitro compounds. Correlation with molecular orbital energies and hydrophobicity.
AID23442Partition coefficient (logP)1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Structure-activity relationship of mutagenic aromatic and heteroaromatic nitro compounds. Correlation with molecular orbital energies and hydrophobicity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (58)

TimeframeStudies, This Drug (%)All Drugs %
pre-19908 (13.79)18.7374
1990's16 (27.59)18.2507
2000's20 (34.48)29.6817
2010's11 (18.97)24.3611
2020's3 (5.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 38.89

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index38.89 (24.57)
Research Supply Index4.09 (2.92)
Research Growth Index4.72 (4.65)
Search Engine Demand Index53.90 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (38.89)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews5 (8.47%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other54 (91.53%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]