Page last updated: 2024-11-05

2,6-dinitrophenol

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

Cross-References

ID SourceID
PubMed CID11312
CHEMBL ID3278560
CHEBI ID39357
SCHEMBL ID1077970
MeSH IDM0150337

Synonyms (40)

Synonym
BB 0259250
STL355968
wln: wnr bq cnw
573-56-8
nsc-6215
o-dinitrophenol
nsc6215
2,6-dinitrophenol
phenol, .beta.-dinitro-
.beta.-dinitrophenol
2,6-dinitrofenol [czech]
ccris 3104
hsdb 6306
einecs 209-357-9
nsc 6215
brn 1913410
phenol, beta-dinitro-
phenol, 2,6-dinitro-
inchi=1/c6h4n2o5/c9-6-4(7(10)11)2-1-3-5(6)8(12)13/h1-3,9
2,6-dinitrophenol, 95%
2,6-dnp
dinitro-2,6-phenol
beta-dinitrophenol
CHEBI:39357 ,
AKOS000274520
f4qm4i92kc ,
2,6-dinitrofenol
unii-f4qm4i92kc
FT-0610716
EPITOPE ID:161741
2,6-dinitro-phenol
2,6-dinitro phenol
CHEMBL3278560
SCHEMBL1077970
2,6-dinitrophenol [mi]
DTXSID5022063
2,6-dinitrophenol 10 microg/ml in acetonitrile
AS-40741
Q20856130
EN300-97958

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" 2,4-DNP and DNOC showed the highest tryptophan fluorescence quenching constant values, these being also the most toxic compounds."( Quenching of tryptophan fluorescence in the presence of 2,4-DNP, 2,6-DNP, 2,4-DNA and DNOC and their mechanism of toxicity.
HuĊ£anu, CA; Pintilie, O; Zaharia, M, 2013
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
dinitrophenolMembers of the class of nitrophenol carrying two nitro substituents.
[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]

Bioassays (10)

Assay IDTitleYearJournalArticle
AID1145606Octanol-aqueous phase partition coefficient, log P of the compound1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145623Uncoupling of oxidative phosphorylation in rat liver mitochondria at pH 7 relative to control1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145614Dissociation constant, pKa of the compound1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145619Octanol-aqueous phase distribution coefficient, log D of the compound at pH 71977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145617Octanol-aqueous phase distribution coefficient, log D of the compound at pH 51977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145620Octanol-aqueous phase distribution coefficient, log D of the compound at pH 81977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145618Octanol-aqueous phase distribution coefficient, log D of the compound at pH 61977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145624Uncoupling of oxidative phosphorylation in rat liver mitochondria at pH 8 relative to control1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145622Uncoupling of oxidative phosphorylation in rat liver mitochondria at pH 6 relative to control1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
AID1145621Uncoupling of oxidative phosphorylation in rat liver mitochondria at pH 5 relative to control1977Journal of medicinal chemistry, Jan, Volume: 20, Issue:1
Use of distribution coefficients in quantitative structure-activity relationships.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (41.67)18.7374
1990's1 (8.33)18.2507
2000's1 (8.33)29.6817
2010's5 (41.67)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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%
Other13 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]