Record Information
Version1.0
Creation Date2016-05-27 02:00:04 UTC
Update Date2016-11-09 01:22:39 UTC
Accession NumberCHEM042369
Identification
Common Namephosphinomethylmalate
ClassSmall Molecule
DescriptionA dicarboxylic acid anion obtained by deprotonation of the carboxy and phosphino group of phosphinomethylmalic acid.
Contaminant Sources
  • FooDB Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
PhosphinomethylmalateChEBI
Phosphinomethylmalic acidGenerator
2-Phosphinomethylmalic acid(3-)Generator
Chemical FormulaC5H6O7P
Average Molecular Mass209.071 g/mol
Monoisotopic Mass208.987 g/mol
CAS Registry NumberNot Available
IUPAC Name2-hydroxy-2-(phosphinatomethyl)butanedioate
Traditional Name2-hydroxy-2-(phosphinatomethyl)butanedioate
SMILESOC(CC([O-])=O)(CP([O-])=O)C([O-])=O
InChI IdentifierInChI=1S/C5H9O7P/c6-3(7)1-5(10,4(8)9)2-13(11)12/h10,13H,1-2H2,(H,6,7)(H,8,9)(H,11,12)/p-3
InChI KeyZKRDXWTUWPUWEG-UHFFFAOYSA-K
Chemical Taxonomy
Description belongs to the class of organic compounds known as short-chain hydroxy acids and derivatives. These are hydroxy acids with an alkyl chain the contains less than 6 carbon atoms.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassHydroxy acids and derivatives
Sub ClassShort-chain hydroxy acids and derivatives
Direct ParentShort-chain hydroxy acids and derivatives
Alternative Parents
Substituents
  • Short-chain hydroxy acid
  • Dicarboxylic acid or derivatives
  • Fatty acid
  • Tertiary alcohol
  • Carboxylic acid derivative
  • Carboxylic acid
  • Organic oxide
  • Organopnictogen compound
  • Organophosphorus compound
  • Organooxygen compound
  • Organic oxygen compound
  • Alcohol
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic anion
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility83.9 g/LALOGPS
logP-0.91ALOGPS
logP-2.4ChemAxon
logS-0.5ALOGPS
pKa (Strongest Acidic)2.15ChemAxon
pKa (Strongest Basic)-4.2ChemAxon
Physiological Charge-3ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area140.62 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity58.88 m³·mol⁻¹ChemAxon
Polarizability15.17 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
SpectraNot Available
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDNot Available
HMDB IDHMDB0304463
FooDB IDFDB031109
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDCPD-11742
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider ID58164168
ChEBI ID91181
PubChem Compound IDNot Available
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=1368511
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=3170341