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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10N4
Molecular Weight 210.2346
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-DIAMINOPHENAZINE

SMILES

NC1=CC2=NC3=CC=CC=C3N=C2C=C1N

InChI

InChIKey=VZPGINJWPPHRLS-UHFFFAOYSA-N
InChI=1S/C12H10N4/c13-7-5-11-12(6-8(7)14)16-10-4-2-1-3-9(10)15-11/h1-6H,13-14H2

HIDE SMILES / InChI

Molecular Formula C12H10N4
Molecular Weight 210.2346
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Spectrophotometric quantification of horseradish peroxidase with o-phenylenediamine.
2010-12-15
Oxidative stress in diabetic kidney disease.
2010
Development of an enzymatic microreactor based on microencapsulated laccase with off-line capillary electrophoresis for measurement of oxidation reactions.
2009-11-20
Metal Oxides and Ion-Exchanging Surfaces as pH Sensors in Liquids: State-of-the-Art and Outlook.
2009
A sensitive resonance scattering spectral assay for the determination of trace H2O2 based on the hrp catalytic reaction and nanogold aggregation.
2008-11
Neurodegenerative diseases of the retina and potential for protection and recovery.
2008-06
2,3-Diamino-phenazine tetra-hydrate.
2008-05-07
[Determination of hydrogen peroxide in rainwater by fluorometry].
2008-04
The study of a chemiluminescence immunoassay using the peroxyoxalate chemiluminescent reaction and its application.
2007-06-15
Chemiluminescent imaging analysis of interferon alpha in serum samples.
2007-02
Liquid chromatographic/mass spectrometric investigation on the reaction products in the peroxidase-catalyzed oxidation of o-phenylenediamine by hydrogen peroxide.
2005-05
Determination of myoglobin based on its enzymatic activity by stopped-flow spectrophotometry.
2005-04
Identification of intermediate and product from methemoglobin-catalyzed oxidation of o-phenylenediamine in two-phase aqueous-organic system.
2005-01
Photoinduced DNA cleavage and cellular damage in human dermal fibroblasts by 2,3-diaminophenazine.
2004-10-21
Identification of 2,3-diaminophenazine and of o-benzoquinone dioxime as the major in vitro metabolites of benzofuroxan.
2004-04
[The study on reaction kinetics based on a new system of the horseradish peroxidase catalyting the oxidation of o-phenylenediamine by H2O2].
2002-06
Chelating activity of advanced glycation end-product inhibitors.
2001-12-28
Electrochemical ELISA for the detection of cucumber mosaic virus using o-pheneylenediamine as substrate.
2001-12-24
Phenazine-2,3-diamine.
2001-01
Hepatitis C viral IRES inhibition by phenazine and phenazine-like molecules.
2000-06-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:27 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:27 GMT 2025
Record UNII
0B20H27U1Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-DIAMINOPHENAZINE [MI]
Preferred Name English
2,3-DIAMINOPHENAZINE
MI  
Systematic Name English
DIAMINOPHENAZINE, 2,3-
Systematic Name English
2,3-PHENAZINEDIAMINE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40984097
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
PUBCHEM
410099
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
FDA UNII
0B20H27U1Y
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-512-0
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
MESH
C054312
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
CAS
655-86-7
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY
MERCK INDEX
m4254
Created by admin on Mon Mar 31 18:42:27 GMT 2025 , Edited by admin on Mon Mar 31 18:42:27 GMT 2025
PRIMARY Merck Index