Oxazolone

CAS No. 15646-46-5

Oxazolone( 4-Ethoxymethylene-2-phenyl-2-oxazolin-5-one )

Catalog No. M19875 CAS No. 15646-46-5

Oxazolone has been used as a haptenizing agent which can induce an inflammatory reaction in adult zebrafish intestinal tissues and this can be used as a model for gene expression studies of the two forms of inflammatory bowel disease like Crohn’s disease and ulcerative colitis.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 28 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG 27 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Oxazolone
  • Note
    Research use only, not for human use.
  • Brief Description
    Oxazolone has been used as a haptenizing agent which can induce an inflammatory reaction in adult zebrafish intestinal tissues and this can be used as a model for gene expression studies of the two forms of inflammatory bowel disease like Crohn’s disease and ulcerative colitis.
  • Description
    Oxazolone has been used as a haptenizing agent which can induce an inflammatory reaction in adult zebrafish intestinal tissues and this can be used as a model for gene expression studies of the two forms of inflammatory bowel disease like Crohn’s disease and ulcerative colitis.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    4-Ethoxymethylene-2-phenyl-2-oxazolin-5-one
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    15646-46-5
  • Formula Weight
    217.22
  • Molecular Formula
    C12H11NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    CCOC=C1N=C(OC1=O)c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Miyauchi K et al. A cyclic form of N6-threonylcarbamoyladenosine as a widely distributed tRNA hypermodification. Nat Chem Biol. 2013 Feb;9(2):105-11.
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