Canmetcon
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Identification
YMDB IDYMDB16162
Name2-Aminoacrylic acid
SpeciesNot Available
StrainBrewer's yeast
DescriptionNot Available
Structure
Thumb
Synonyms
  • 2,3-Didehydroalanine
  • 2-Aminoacrylate
  • alpha,beta-Dehydroalanine
  • Anhydroserine2-aminopropenoic acid
  • Dehydroalanine
  • 2-Aminoprop-2-enoate
  • a,b-Dehydroalanine
  • Α,β-dehydroalanine
  • Anhydroserine2-aminopropenoate
  • 2-Aminoprop-2-enoic acid
  • (alpha)-(beta)-Di-dehydroalanine
  • a-b-Di-dehydroalanine
  • alpha-beta-Di-dehydroalanine
  • alpha-Aminoacrylate
CAS numberNot Available
WeightAverage: 87.0773
Monoisotopic: 87.032028409
InChI KeyUQBOJOOOTLPNST-UHFFFAOYSA-N
InChIInChI=1S/C3H5NO2/c1-2(4)3(5)6/h1,4H2,(H,5,6)
IUPAC Name2-aminoprop-2-enoic acid
Traditional IUPAC Namedehydroalanine
Chemical FormulaC3H5NO2
SMILESNC(=C)C(O)=O
Chemical Taxonomy
Description belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentAlpha amino acids
Alternative Parents
Substituents
  • Alpha-amino acid
  • Amino acid
  • Carboxylic acid
  • Enamine
  • Monocarboxylic acid or derivatives
  • Hydrocarbon derivative
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Amine
  • Primary aliphatic amine
  • Organic nitrogen compound
  • Carbonyl group
  • Organic oxygen compound
  • Organic oxide
  • Organopnictogen compound
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Physical Properties
StateSolid
Charge0
Melting pointNot Available
Experimental Properties
PropertyValueReference
Water SolubilityNot AvailablePhysProp
LogPNot AvailablePhysProp
Predicted Properties
PropertyValueSource
Water Solubility233 g/LALOGPS
logP-0.13ALOGPS
logP-2.9ChemAxon
logS0.43ALOGPS
pKa (Strongest Acidic)2.58ChemAxon
pKa (Strongest Basic)8.64ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area63.32 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity20.92 m³·mol⁻¹ChemAxon
Polarizability7.72 ųChemAxon
Number of Rings0ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Biological Properties
Cellular LocationsNot Available
Organoleptic PropertiesNot Available
SMPDB Pathways
Sulfur metabolismPW002483 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG Pathways
Sulfur metabolismec00920 Map00920
SMPDB Reactions
L-Cysteinehydron + Hydrogen sulfide + 2-Aminoacrylic acid
KEGG ReactionsNot Available
Concentrations
Intracellular ConcentrationsNot Available
Extracellular ConcentrationsNot Available
Spectra
Spectra
References
References:Not Available
Synthesis Reference:Not Available
External Links:
ResourceLink
CHEBI ID17123
HMDB IDHMDB0003609
Pubchem Compound ID123991
Kegg IDC02218
ChemSpider ID110510
FOODB IDFDB023206
Wikipedia IDNot Available
BioCyc IDNot Available

Enzymes

General function:
Involved in cysteine biosynthetic process from serine
Specific function:
O(3)-acetyl-L-serine + H(2)S = L-cysteine + acetate
Gene Name:
Not Available
Uniprot ID:
P53206
Molecular weight:
42800.5
Reactions
O(3)-acetyl-L-serine + H(2)S → L-cysteine + acetate.