Page last updated: 2024-11-05

naphthol yellow

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

Description

naphthol yellow: RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

flavianic acid : A naphthalenesulfonic acid that is naphthalene-2-sulfonic acid substituted by nitro groups at positions 5 and 7 as well as a hydroxy group at position 8. The disodium salt is the biological stain 'naphthol yellow S'. [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 CID10226
CHEMBL ID1461018
CHEBI ID87221
SCHEMBL ID93200
MeSH IDM0054879

Synonyms (52)

Synonym
LS-13737
naphthol yellow
2-naphthalenesulfonic acid, 8-hydroxy-5,7-dinitro-
8-hydroxy-5,7-dinitro-naphthalene-2-sulfonic acid
2,4-dinitronaphtholsulfonic acid
nsc-243753
nsc243753
flavianic acid
483-84-1
2-naphthalenesulfonic acid,7-dinitro-
dnns
CBDIVE_004212
8-hydroxy-5,5-dinitro-2-naphthalenesulfonic acid (8ci)(9ci)
NCGC00091716-01
nsc 243753
2-naphthalenesulfonic acid, 5,7-dinitro-8-hydroxy-
einecs 207-600-3
ai3-03274
brn 2708476
2,4-dinitro-1-naphthol-7-sulfonic acid
8-hydroxy-5,7-dinitronaphthalene-2-sulphonic acid
8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid
STK301629
nsc-244041
8-hydroxy-5,7-dinitronaphthalene-2-sulfonic acid
8-hydroxy-5,5-dinitro-2-naphthalenesulfonic acid
2,4-dinitro-1-naphtho-7-sulfonic acid
F0012
AKOS003791115
NCGC00091716-02
tox21_201142
cas-483-84-1
dtxcid305167
dtxsid4025167 ,
NCGC00258694-01
BBL013045
4i7kxl5kl5 ,
4-11-00-00617 (beilstein handbook reference)
unii-4i7kxl5kl5
flavianic acid hydrate
FT-0632196
AKOS015894269
SCHEMBL93200
chebi:87221 ,
CHEMBL1461018
8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid #
FCQJEPASRCXVCB-UHFFFAOYSA-N
SR-01000196124-1
sr-01000196124
2-4-dinitro-1-naphthol-7-sulfonic acid
Q27159452
CS-0452786
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
histological dyeA dye used in microscopic or electron microscopic examination of cells and tissues to give contrast and to highlight particular features of interest, such as nuclei and cytoplasm.
[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 (3)

ClassDescription
naphtholsAny hydroxynaphthalene derivative that has a single hydroxy substituent.
naphthalenesulfonic acid
C-nitro compoundA nitro compound having the nitro group (-NO2) attached to a carbon atom.
[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 (13)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency10.00000.003245.467312,589.2998AID2517
Chain A, TYROSYL-DNA PHOSPHODIESTERASEHomo sapiens (human)Potency10.00000.004023.8416100.0000AID485290
LuciferasePhotinus pyralis (common eastern firefly)Potency44.52970.007215.758889.3584AID1224835
acetylcholinesteraseHomo sapiens (human)Potency49.03890.002541.796015,848.9004AID1347395; AID1347397; AID1347399
AR proteinHomo sapiens (human)Potency68.17130.000221.22318,912.5098AID1259243
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency39.81070.011212.4002100.0000AID1030
pregnane X nuclear receptorHomo sapiens (human)Potency24.18810.005428.02631,258.9301AID1346982
thyroid stimulating hormone receptorHomo sapiens (human)Potency62.55790.001628.015177.1139AID1259385; AID1259395
Histone H2A.xCricetulus griseus (Chinese hamster)Potency112.31600.039147.5451146.8240AID1224845
15-hydroxyprostaglandin dehydrogenase [NAD(+)] isoform 1Homo sapiens (human)Potency8.91250.001815.663839.8107AID894
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.00180.010039.53711,122.0200AID588545
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency24.18810.000323.4451159.6830AID743065
nuclear factor NF-kappa-B p105 subunit isoform 1Homo sapiens (human)Potency50.11874.466824.832944.6684AID651749
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-199020 (64.52)18.7374
1990's4 (12.90)18.2507
2000's3 (9.68)29.6817
2010's2 (6.45)24.3611
2020's2 (6.45)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 36.06

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 Index36.06 (24.57)
Research Supply Index3.56 (2.92)
Research Growth Index4.29 (4.65)
Search Engine Demand Index45.59 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (36.06)

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%
Other34 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]