Showing metabocard for Pyruvatoxime (BMDB0002455)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 22:55:27 UTC
Update Date2020-04-22 15:11:02 UTC
BMDB IDBMDB0002455
Secondary Accession Numbers
  • BMDB02455
Metabolite Identification
Common NamePyruvatoxime
DescriptionPyruvatoxime belongs to the class of organic compounds known as ketoximes. These are organic compounds with the general formula RC(R')=NOH (R,R' = organyl). Based on a literature review very few articles have been published on Pyruvatoxime.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
2-(hydroxyimino)PropanoateHMDB
2-(hydroxyimino)Propanoic acidHMDB
2-OximinopropanoateHMDB
2-Oximinopropanoic acidHMDB, MeSH
Pyruvate oximeHMDB
Pyruvic oximeHMDB, MeSH
2-Oximinopropanoic acid, ion (1-)MeSH, HMDB
(2E)-2-(Hydroxyimino)propanoateGenerator, HMDB
PyruvatoximeMeSH
Chemical FormulaC3H5NO3
Average Molecular Weight103.0767
Monoisotopic Molecular Weight103.026943031
IUPAC Name(2E)-2-(hydroxyimino)propanoic acid
Traditional Namepyruvic oxime
CAS Registry Number2211-14-5
SMILES
C\C(=N/O)C(O)=O
InChI Identifier
InChI=1S/C3H5NO3/c1-2(4-7)3(5)6/h7H,1H3,(H,5,6)/b4-2+
InChI KeyMVGBKLTYYAYYGY-DUXPYHPUSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as ketoximes. These are organic compounds with the general formula RC(R')=NOH (R,R' = organyl).
KingdomOrganic compounds
Super ClassOrganic nitrogen compounds
ClassOrganonitrogen compounds
Sub ClassOximes
Direct ParentKetoximes
Alternative Parents
Substituents
  • Ketoxime
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cytoplasm
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water Solubility902 mg/mLNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-0.45ALOGPS
logP0.075ChemAxon
logS-0.8ALOGPS
pKa (Strongest Acidic)3.42ChemAxon
pKa (Strongest Basic)-2.6ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area69.89 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity21.81 m³·mol⁻¹ChemAxon
Polarizability8.71 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0002455
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023008
KNApSAcK IDNot Available
Chemspider ID4925178
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID6687
PubChem Compound6419427
PDB IDKG7
ChEBI IDNot Available
References
Synthesis ReferenceCastignetti D; Forgue C J; Sclafani L A Pathway of oxidation of pyruvic oxime by a heterotrophic nitrifier of the genus Alcaligenes: evidence against nitroethane as an intermediate. Archives of biochemistry and biophysics (1986), 250(1), 228-32.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available