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Details

Stereochemistry ACHIRAL
Molecular Formula C12H7Cl2NO2
Molecular Weight 268.095
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DICHLOROINDOPHENOL

SMILES

OC1=CC=C(C=C1)N=C2C=C(Cl)C(=O)C(Cl)=C2

InChI

InChIKey=CCBICDLNWJRFPO-UHFFFAOYSA-N
InChI=1S/C12H7Cl2NO2/c13-10-5-8(6-11(14)12(10)17)15-7-1-3-9(16)4-2-7/h1-6,16H

HIDE SMILES / InChI

Molecular Formula C12H7Cl2NO2
Molecular Weight 268.095
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification and characterization of the enzymatic activity of zeta-crystallin from guinea pig lens. A novel NADPH:quinone oxidoreductase.
1992 Jan 5
Novel test and its automation for the determination of erythrocyte acetylcholinesterase and its application to organophosphate exposure.
2001 Jan
Molecular and biochemical characterization of a cytokinin oxidase from maize.
2001 Jan
[Activities of the liver microsome reductases in adult and aged rats during stress].
2001 Nov-Dec
[Reductase activity in the liver microsomes in adult and old rats during immobilization stress].
2001 Sep-Oct
Screening for the carriers of thalassemias and abnormal hemoglobins at the community level.
2002
Effects of Ca(2+)-activated calmodulin on neuronal nitric oxide synthase reductase activity and binding of substrates: pH dependence of kinetic parameters.
2002 Jan 8
CNS neurons express two distinct plasma membrane electron transport systems implicated in neuronal viability.
2002 Nov
Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase.
2002 Nov 12
L-Serine, D- and L-proline and alanine as respiratory substrates of Helicobacter pylori: correlation between in vitro and in vivo amino acid levels.
2003 Aug
Photoinhibition and recovery of photosynthesis in leaves of Vitis berlandieri and Vitis rupestris.
2004 Feb
A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia.
2004 May
The chemical mechanism of action of glucose oxidase from Aspergillus niger.
2004 May
Electrochemical investigation of the dynamics of Mycobacterium smegmatis cells' transformation to dormant, nonculturable form.
2004 Sep
[Analysis of vitamin C in the biologically active supplements to food and food products enriched with micronutrients].
2005
Development of a commercial amperometric biosensor electrode for the ketone D-3-hydroxybutyrate.
2005 Feb 15
Pachypodol from Croton ciliatoglanduliferus Ort. as water-splitting enzyme inhibitor on thylakoids.
2006 Feb 22
Parameters for cellular viability and membrane function in chenopodium cells show a specific response of extracellular pH to heat shock with extreme Q10.
2006 Jan
Reassessment of a simple chemical method using DCIP for screening for haemoglobin E.
2006 Jan
Biotransformation of malachite green by Saccharomyces cerevisiae MTCC 463.
2006 Mar
Sensitivity and specificity of dichlorophenol--indophenol precipitation test to screen for the hemoglobin E trait in pregnant women.
2006 Nov
Escherichia coli-catalyzed bioelectrochemical oxidation of acetate in the presence of mediators.
2006 Sep
Spectrophotometric assay for complex I of the respiratory chain in tissue samples and cultured fibroblasts.
2007 Apr
[Oxygen can be replaced by artificial electron acceptors in reactions catalyzed by alcohol oxidase].
2007 Jan-Feb
Reconstitution of the water-oxidizing complex in manganese-depleted photosystem II preparations using synthetic binuclear Mn(II) and Mn(IV) complexes: production of hydrogen peroxide.
2007 Jul-Sep
Decolourization of azo dye methyl red by Saccharomyces cerevisiae MTCC 463.
2007 Jun
A simple and highly repeatable colorimetric toxicity assay method using 2,6-dichlorophenolindophenol as the redox color indicator and whole eukaryote cells.
2007 Oct
Isolation and characterization of photosystem II from the filamentous sporophyte of Porphyra yezoensis.
2008 Aug
Snapshots of catalysis in the E1 subunit of the pyruvate dehydrogenase multienzyme complex.
2008 Dec 10
Antibiotic susceptibility testing at a screen-printed carbon electrode array.
2008 Feb 1
Decylubiquinol impedes mitochondrial respiratory chain complex I activity.
2008 Jul
Low cost combination of DCIP and MCV was better than that of DCIP and OF in the screening for hemoglobin E.
2008 Oct
The stabilizing effects of immobilization in D-amino acid oxidase from Trigonopsis variabilis.
2008 Sep 17
Production, characterization and determination of the real catalytic properties of the putative 'succinate dehydrogenase' from Wolinella succinogenes.
2009 Mar
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:18:21 GMT 2023
Edited
by admin
on Fri Dec 15 18:18:21 GMT 2023
Record UNII
C35QN2Z58B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DICHLOROINDOPHENOL
Common Name English
2,6-DICHLORO-N-4-HYDROXYPHENYL-P-BENZOQUINONE MONOIMINE
Common Name English
DCIP
Common Name English
TILLMANS REAGENT
Common Name English
Code System Code Type Description
CAS
956-48-9
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
PUBCHEM
13726
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
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EPA CompTox
DTXSID7061352
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
ALANWOOD
DCIP
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
FDA UNII
C35QN2Z58B
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
CHEBI
945
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
WIKIPEDIA
Dichlorophenolindophenol
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
213-479-8
Created by admin on Fri Dec 15 18:18:21 GMT 2023 , Edited by admin on Fri Dec 15 18:18:21 GMT 2023
PRIMARY