Showing metabocard for Aminoacetone (BMDB0002134)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesenzymes (1) Show 1 proteinXML
Record Information
Version1.0
Creation Date2016-09-30 22:51:32 UTC
Update Date2020-05-21 16:28:59 UTC
BMDB IDBMDB0002134
Secondary Accession Numbers
  • BMDB02134
Metabolite Identification
Common NameAminoacetone
DescriptionAminoacetone belongs to the class of organic compounds known as alpha-amino ketones. These are ketones containing a carboxylic acid, and an amine group attached to the alpha carbon atom relative to C=O group. Aminoacetone exists in all living species, ranging from bacteria to plants to humans. Based on a literature review a significant number of articles have been published on Aminoacetone.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Amino-2-propanoneChEBI
1-AMINO-propan-2-oneChEBI
1-amino-(8CI,9ci)-2-propanoneHMDB
1-Aminopropan-2-oneHMDB, MeSH
alpha-AminoacetoneHMDB
amino-(6CI)-2-propanoneHMDB
amino-2-PropanoneHMDB
AmmonioacetoneHMDB
Chemical FormulaC3H7NO
Average Molecular Weight73.0938
Monoisotopic Molecular Weight73.052763851
IUPAC Name1-aminopropan-2-one
Traditional Nameα-aminoacetone
CAS Registry Number298-08-8
SMILES
CC(=O)CN
InChI Identifier
InChI=1S/C3H7NO/c1-3(5)2-4/h2,4H2,1H3
InChI KeyBCDGQXUMWHRQCB-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as alpha-amino ketones. These are ketones containing a carboxylic acid, and an amine group attached to the alpha carbon atom relative to C=O group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentAlpha-amino ketones
Alternative Parents
Substituents
  • Alpha-aminoketone
  • Organic nitrogen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Primary amine
  • Organonitrogen compound
  • Primary aliphatic amine
  • Amine
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Mitochondria
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-1.3ALOGPS
logP-0.82ChemAxon
logS0.86ALOGPS
pKa (Strongest Acidic)17.3ChemAxon
pKa (Strongest Basic)7.84ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area43.09 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity19.55 m³·mol⁻¹ChemAxon
Polarizability7.71 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular Locations
  • Mitochondria
Biospecimen Locations
  • Spleen
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SpleenExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
 details
Abnormal Concentrations
Not Available
HMDB IDHMDB0002134
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022860
KNApSAcK IDNot Available
Chemspider ID210
KEGG Compound IDC01888
BioCyc IDNot Available
BiGG ID38629
Wikipedia Link1-Amino-2-propanone
METLIN ID6502
PubChem Compound215
PDB IDNot Available
ChEBI ID17906
References
Synthesis ReferenceTurner, J. M. Aminoacetone production by microorganisms. Biochemical Journal (1966), 98(1), 7P.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Enzymes

Enzyme Details
1. Amine oxidase [flavin-containing] A
General function:
Amino acid transport and metabolism
Specific function:
Catalyzes the oxidative deamination of biogenic and xenobiotic amines and has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAOA preferentially oxidizes biogenic amines such as 5-hydroxytryptamine (5-HT), norepinephrine and epinephrine.
Gene Name:
MAOA
Uniprot ID:
P21398
Molecular weight:
59758.0
Reactions
Aminoacetone + Oxygen + Water → Ammonia + Hydrogen peroxide + Pyruvaldehydedetails