Page last updated: 2024-11-05

ponceau 3r

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

Description

Ponceau 3R is a synthetic azo dye. It is derived from naphthalene and contains two sulfonic acid groups. The dye is bright red in color and is used in a variety of applications, including food coloring, textiles, and cosmetics. Ponceau 3R is considered safe for use in food products in many countries. Ponceau 3R can be synthesized via a multi-step process. The first step involves the diazotization of 1-naphthylamine with sodium nitrite and hydrochloric acid. The diazonium salt is then coupled with 2-naphthol, yielding Ponceau 3R. Despite being commonly used in food products, there have been some studies suggesting that Ponceau 3R may be a possible carcinogen. Further research is needed to confirm these findings. The dye has been found to induce hyperactivity in children, but there is no consensus on this finding. Ponceau 3R is often studied because it is a common food additive and has been linked to potential health risks. This dye is also used as a coloring agent in some pharmaceuticals. Research on Ponceau 3R often focuses on its safety and potential health effects. The dye's potential genotoxicity is being investigated to determine if it poses a carcinogenic risk. The potential for Ponceau 3R to cause allergic reactions is also under investigation. '

ponceau 3R: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID19095
CHEMBL ID3186386
CHEBI ID176136
SCHEMBL ID3624402
SCHEMBL ID1268489
SCHEMBL ID1268487
MeSH IDM0074226

Synonyms (75)

Synonym
disodium;3-hydroxy-4-[(2,4,5-trimethylphenyl)diazenyl]naphthalene-2,7-disulonate
CHEBI:176136
disodium 3-hydroxy-4-[(e)-(2,4,5-trimethylphenyl)diazenyl]naphthalene-2,7-disulfonate
c.i.16155
fd & c red no. 1
usacert red no. 1
maple ponceau 3r
a.f. red no. 1
c.i. food red 6
food red 6
ext d and c red no. 15
c.i. food red 6, disodium salt
3564-09-8
nsc-10461
ponceau 3r lake
nsc10461
ponceau 3r
ponceau rn
fdc red 1
ponceau 3rn
dolkwal ponceau 3r
d and c red 15
ponceau 3r sodium salt
nsc 10461
einecs 222-638-0
disodium 3-hydroxy-4-((2,4,5-trimethylphenyl)azo)naphthalene-2,7-disulphonate
3-hydroxy-4((2,4,5-trimethylphenyl)azo)-2,7-naphthalenedisulfonic
ccris 527
cerven kumidinova [czech]
3-hydroxy-4-((2,4,5-trimethylphenyl)azo)-2,7-naphthalenedisulfonic acid disodium salt
3-hydroxy-4-((2,4,5-trimethylphenyl)azo)-2,7-naphthalenedisulphonic acid, disodium salt
cerven potravinarska 6 [czech]
disodium 3-hydroxy-4-((2,4,5-trimethylphenyl)azo)-2,7-naphthalenedisulphonate
sodium cumeneazo-beta-naphthol disulphonate
disodium 3-hydroxy-4-((2,4,5-trimethylphenyl)azo)-2,7-naphthalenedisulfonate
sodium cumeneazo-beta-naphtholdisulphonate
2,7-naphthalenedisulfonic acid, 3-hydroxy-4-((2,4,5-trimethylphenyl)azo)-, disodium salt
hsdb 2946
ci 16155
af red no. 1
sodium cumeneazo-beta-naphthol disulfonate
ci food 6
ci food red 6, disodium salt
SCHEMBL3624402
dtxcid801231
tox21_202788
NCGC00260334-01
cas-3564-09-8
dtxsid7021231 ,
cerven kumidinova
unii-fa32r9s74x
fa32r9s74x ,
cerven potravinarska 6
FT-0634904
ponceau 3r [iarc]
aka502
ponceau 3r [ii]
c.i. food red 6 disodium salt
ponceau 3r [hsdb]
fd&c red no. 1 (delisted)
red no. 502
ponceau 3r [mi]
aka502 [inci]
2,7-naphthalenedisulfonic acid, 3-hydroxy-4-(2-(2,4,5-trimethylphenyl)diazenyl)-, sodium salt (1:2)
SCHEMBL1268489
SCHEMBL1268487
ponceau3r
CHEMBL3186386
ponceau 3r, analytical standard
pon-ceau 3r
sodium (e)-3-hydroxy-4-((2,4,5-trimethylphenyl)diazenyl)naphthalene-2,7-disulfonate
allylorthoformate
disodium 3-hydroxy-4-[(2,4,5-trimethylphenyl)azo]-2,7-naphthalenedisulfonate
STARBLD0009511
disodium;3-hydroxy-4-[(2,4,5-trimethylphenyl)diazenyl]naphthalene-2,7-disulfonate

Research Excerpts

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
progesterone receptorHomo sapiens (human)Potency0.12080.000417.946075.1148AID1346784
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency0.95930.001530.607315,848.9004AID1224841
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency0.544119.739145.978464.9432AID1159509
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (55.56)18.7374
1990's0 (0.00)18.2507
2000's1 (11.11)29.6817
2010's2 (22.22)24.3611
2020's1 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.98

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index23.98 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index4.73 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.98)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]