Page last updated: 2024-12-05

1-nitroso-2-naphthol

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

1-Nitroso-2-naphthol, also known as α-nitroso-β-naphthol, is an organic compound with the formula C10H7NO2. It is a yellow crystalline solid that is sparingly soluble in water but soluble in organic solvents. 1-Nitroso-2-naphthol is used as a reagent in analytical chemistry, particularly for the colorimetric determination of metals such as cobalt, copper, and iron. Its synthesis involves the nitrosation of 2-naphthol using nitrous acid. The compound exhibits chelating properties, forming colored complexes with metal ions. Its importance stems from its use in analytical techniques and its ability to act as a ligand in coordination chemistry. Research on 1-Nitroso-2-naphthol focuses on its analytical applications, its coordination chemistry with various metal ions, and its potential for use in other fields such as catalysis and material science.'

Cross-References

ID SourceID
PubMed CID8580
CHEBI ID194993
SCHEMBL ID8947876
SCHEMBL ID103998
MeSH IDM0084557

Synonyms (74)

Synonym
AC-18344
1-nitroso-naphthalen-2-ol
.alpha.-nitroso-.beta.-naphthol
2-naphthalenol, 1-nitroso-
131-91-9
1-nitroso-2-naphthol ,
nitroso-.beta.-naphthol
.alpha.-nitrosonaphthol
nsc4151
wln: l66j bno cq
nsc-4151
2-naphthol, 1-nitroso-
1-nitrosonaphthalen-2-ol
nsc-677525
nsc677525
ai3-09078
nsc 4151
nitroso-beta-naphthol
1-nitroso-2-naftol [czech]
ccris 1556
einecs 205-043-0
zelen moridlova 4 [czech]
brn 0776947
alpha-nitroso-beta-naftol [czech]
nsc107835
2636-79-5
nsc-107835
.alpha.-nitroso-.beta.-naphthol oxime
1,2-naphthoquinone 1-oxime
1-nitroso-2-naphthol, 97%
STK391542
AKOS000283071
N0266
STK802252
(1e)-1-(hydroxyimino)naphthalen-2(1h)-one
CHEBI:194993
A806332
AKOS005622627
BBL000016
AKOS006279793
alpha-nitroso-beta-naftol
unii-757i55u2qx
zelen moridlova 4
757i55u2qx ,
1-nitroso-2-naftol
4-07-00-02419 (beilstein handbook reference)
BBL011067
(e)-1-(hydroxyimino)naphthalen-2(1h)-one
FT-0608158
AE-562/40186369
alpha-nitroso-beta-naphthol
SCHEMBL8947876
SCHEMBL103998
1‐nitroso‐2‐naphthol (substrate 5)
bdbm108228
1-nitroso-2-naphthalenol
1-nitroso-2-naphthol [mi]
1-nitrosonaphthalene-2-ol
DTXSID9059622
1,2-naphthalenedione, 1-oxime
CAQHPYSDQFDJAL-KHPPLWFESA-N
.alpha.-nitroso-.beta.-naftol
W-108324
mfcd00003884
1-nitroso-2-naphthol, saj special grade, >=97.0%
1-nitroso-2-naphthol, 98.0%
1,2-naphthoquinone-1-oxime
DTXSID30876194
Q3596764
AS-15422
H11769
CS-0336127
EN300-21463
1-(hydroxyimino)naphthalen-2(1h)-one
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
naphtholsAny hydroxynaphthalene derivative that has a single hydroxy substituent.
[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 (1)

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 (7)

Processvia Protein(s)Taxonomy
ubiquinone biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
isoprenoid biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
pyridoxine biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
thiamine biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
isoprenoid biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
thiamine biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
terpenoid biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
1-deoxy-D-xylulose 5-phosphate biosynthetic process1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (7)

Processvia Protein(s)Taxonomy
magnesium ion binding1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
1-deoxy-D-xylulose-5-phosphate synthase activity1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
transferase activity1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
transketolase or transaldolase activity1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
thiamine pyrophosphate binding1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
protein homodimerization activity1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
metal ion binding1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
cytosol1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
cytosol1-deoxy-D-xylulose-5-phosphate synthaseEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1800220DXP Synthase Inhibition Assay from Article 10.1002/cbic.201300187: \\DXP synthase-catalyzed C-N bond formation: nitroso substrate specificity studies guide selective inhibitor design.\\2013Chembiochem : a European journal of chemical biology, Jul-22, Volume: 14, Issue:11
DXP synthase-catalyzed C-N bond formation: nitroso substrate specificity studies guide selective inhibitor design.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-199016 (69.57)18.7374
1990's3 (13.04)18.2507
2000's0 (0.00)29.6817
2010's4 (17.39)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 36.10

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 Index36.10 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index4.74 (4.65)
Search Engine Demand Index46.01 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (36.10)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other24 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]