Record Information Version
1.0 Update Date
1/22/2018 11:54:54 AM
Metabolite ID PAMDB110095
Identification Name:
dialurate Description: Not Available
Structure
Synonyms:
Chemical Formula:
C4 H4 N2 O4
Average Molecular Weight:
144.0171066272 Monoisotopic Molecular
Weight:
144.0171066272 InChI Key:
BVEWMNTVZPFPQI-UHFFFAOYSA-N InChI:
InChI=1S/C4H4N2O4/c7-1-2(8)5-4(10)6-3(1)9/h1,7H,(H2,5,6,8,9,10) CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: C1(=O)(NC(=O)C(O)C(=O)N1)
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as barbituric acid derivatives. These are compounds containing a perhydropyrimidine ring substituted at C-2, -4 and -6 by oxo groups.
Kingdom
Organic compounds Super Class Organoheterocyclic compounds
Class
Diazines Sub Class Pyrimidines and pyrimidine derivatives
Direct Parent
Barbituric acid derivatives Alternative Parents
Substituents
Barbiturate N-acyl urea Ureide 1,3-diazinane 1,3-dicarbonyl compound Dicarboximide Carbonic acid derivative Secondary alcohol Urea Carboxylic acid derivative Azacycle Organonitrogen compound Hydrocarbon derivative Organic oxide Organopnictogen compound Organic oxygen compound Alcohol Carbonyl group Organic nitrogen compound Organooxygen compound Aliphatic heteromonocyclic compound Molecular Framework
Aliphatic heteromonocyclic compounds External Descriptors
barbiturates (CHEBI:76452)
Physical Properties State:
Not Available Charge: Not Available
Melting point:
Not Available Experimental Properties:
Not Available Predicted Properties
Biological Properties Cellular Locations:
Not Available Reactions:
Pathways:
adenosylcobalamin biosynthesis II (late cobalt incorporation)P381-PWY 5,6-dimethylbenzimidazole biosynthesisPWY-5523 adenosylcobalamin biosynthesis from cobyrinate a,c -diamide IIPWY-5508
Spectra Spectra:
Not Available
References References:
Not Available Synthesis Reference:
Not Available Material Safety Data Sheet (MSDS)
Not Available
Links External Links:
This project is supported by
the University of Maryland ,
School of Pharmacy ,
Mass Spectrometry Center , a Waters Center of Excellence. The center is an NIH-investigator funded research and core facility that supports a wide range of cutting-edge metabolomic studies. The Center is supported through a center grant from the University of Maryland and NIH grants to its members. The PAMDB project is affiliated with
The Metabolomics Innovation Centre (TMIC) a leading metabolomics research and service center funded through Genome Alberta, Genome British Columbia and Genome Canada.
