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Home - Products - Proteasome/Ubiquitin - Endogenous Metabolite - DL-3-AMINOISOBUTYRIC ACID

DL-3-AMINOISOBUTYRIC ACID

CAS No. 144-90-1

DL-3-AMINOISOBUTYRIC ACID ( 3-Amino-2-methylpropanoic acid;α-Methyl-β-alanine )

Catalog No. M19753 CAS No. 144-90-1

beta-aminoisobutyric acid is the product from the conversion of N-carbamyl-beta-aminoisobutyric acid by the enzyme Beta-ureidopropionase (EC 3.5.1.6) the last step in pyrimidine degradation. Beta-ureidopropionase deficiency is an inborn error of pyrimidine degradation associated with neurological abnormalities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    DL-3-AMINOISOBUTYRIC ACID
  • Note
    Research use only not for human use.
  • Brief Description
    beta-aminoisobutyric acid is the product from the conversion of N-carbamyl-beta-aminoisobutyric acid by the enzyme Beta-ureidopropionase (EC 3.5.1.6) the last step in pyrimidine degradation. Beta-ureidopropionase deficiency is an inborn error of pyrimidine degradation associated with neurological abnormalities.
  • Description
    beta-aminoisobutyric acid is the product from the conversion of N-carbamyl-beta-aminoisobutyric acid by the enzyme Beta-ureidopropionase (EC 3.5.1.6) the last step in pyrimidine degradation. Beta-ureidopropionase deficiency is an inborn error of pyrimidine degradation associated with neurological abnormalities.
  • Synonyms
    3-Amino-2-methylpropanoic acid;α-Methyl-β-alanine
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    Human Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    144-90-1
  • Formula Weight
    103.12
  • Molecular Formula
    C4H9NO2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    CC(CN)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Kuilenburg A B P V Meinsma R Beke E et al. beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities.[J]. Human Molecular Genetics 2004 13(22):2793-2801.
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