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Details

Stereochemistry ACHIRAL
Molecular Formula C4H3N3O4
Molecular Weight 157.0843
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VIOLURIC ACID

SMILES

ON=C1C(=O)NC(=O)NC1=O

InChI

InChIKey=JMUJZTASUDOAGC-UHFFFAOYSA-N
InChI=1S/C4H3N3O4/c8-2-1(7-11)3(9)6-4(10)5-2/h11H,(H2,5,6,8,9,10)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Biobleaching of eucalypt kraft pulp with a two laccase-mediator stages sequence.
2010-09
Characterization of an extracellular laccase, PbLac1, purified from Polyporus brumalis.
2010-08
Electrochemical and AFM characterization on gold and carbon electrodes of a high redox potential laccase from Fusarium proliferatum.
2010-08
Biodegradability of kraft mill TCF biobleaching effluents: application of enzymatic laccase-mediator system.
2010-04
Influence of very low doses of mediators on fungal laccase activity - nonlinearity beyond imagination.
2009-09-04
Performance and efficiency of old newspaper deinking by combining cellulase/hemicellulase with laccase-violuric acid system.
2009-05
Improving the functional expression of a Bacillus licheniformis laccase by random and site-directed mutagenesis.
2009-02-23
Laccase-mediator system in the decolorization of different types of recalcitrant dyes.
2009-01
Characterization of radical intermediates in laccase-mediator systems. A multifrequency EPR, ENDOR and DFT/PCM investigation.
2008-12-28
Mediator-assisted decolorization and detoxification of textile dyes/dye mixture by Cyathus bulleri laccase.
2008-12
Engineering and Applications of fungal laccases for organic synthesis.
2008-11-20
Comparative study of the efficiency of synthetic and natural mediators in laccase-assisted bleaching of eucalyptus kraft pulp.
2008-11
The influence of operating parameters on the biodelignification of Eucalyptus globulus kraft pulps in a laccase--violuric acid system.
2008-04
Degradation of polycyclic aromatic hydrocarbons by Rigidoporus lignosus and its laccase in the presence of redox mediators.
2008-04
Ammonium violurate: a compact structure with extensive hydrogen bonding in three dimensions.
2007-10
Decolorization of direct dyes by salt fractionated turnip proteins enhanced in the presence of hydrogen peroxide and redox mediators.
2007-09
Violuric acid monohydrate: a second polymorph with more extensive hydrogen bonding.
2007-06
Production, purification and partial characterisation of a novel laccase from the white-rot fungus Panus tigrinus CBS 577.79.
2007-01
Potential applications of the oxidoreductive enzymes in the decolorization and detoxification of textile and other synthetic dyes from polluted water: a review.
2006-11-11
Heterologous expression of lcc1 gene from Trametes trogii in Pichia pastoris and characterization of the recombinant enzyme.
2006-10-12
A pre-concentration procedure using coprecipitation for determination of lead and iron in several samples using flame atomic absorption spectrometry.
2006-08-04
Hydrogen-bonding and carbonyl-carbonyl interactions in violuric acid methanol solvate.
2005-12
A novel method for the spectrophotometric determination of nitrite in water.
2005-06-15
Laccase-mediator biobleaching applied to a direct yellow dyed paper.
2004-12-04
Hydrogen bonding between histidine and lignin model compounds or redox mediators as calculated with the DFT method. Effects on the ease of oxidation.
2004-02-21
Determination of barbituric acid, utilizing a rapid and simple colorimetric assay.
2002-07-31
Fep1, an iron sensor regulating iron transporter gene expression in Schizosaccharomyces pombe.
2002-06-21
Use of laccase together with redox mediators to decolourize Remazol Brilliant Blue R.
2001-08-23
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.
1994-08-17
Name Type Language
NSC-56338
Preferred Name English
VIOLURIC ACID
MI  
Common Name English
ALLOXAN 5-OXIME
Systematic Name English
5-(HYDROXYIMINO)BARBITURIC ACID
Systematic Name English
VIOLURIC ACID [MI]
Common Name English
5-ISONITROSOBARBITURIC ACID
Common Name English
2,4,5,6(1H,3H)-PYRIMIDINETETRONE 5-OXIME
Systematic Name English
Code System Code Type Description
PUBCHEM
6399005
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-741-4
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
CAS
87-39-8
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
WIKIPEDIA
Violuric acid
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID8058954
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
FDA UNII
05RFR8AC84
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY
MERCK INDEX
m11466
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY Merck Index
NSC
56338
Created by admin on Mon Mar 31 21:22:35 GMT 2025 , Edited by admin on Mon Mar 31 21:22:35 GMT 2025
PRIMARY