FR054 (b)

CAS No. 10378-06-0

FR054 (b)( (6R)-FR054 )

Catalog No. M23246 CAS No. 10378-06-0

FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 29 In Stock
5MG 29 In Stock
10MG 37 In Stock
25MG 57 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    FR054 (b)
  • Note
    Research use only, not for human use.
  • Brief Description
    FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.
  • Description
    FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    (6R)-FR054
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    Apoptosis|PGM3
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    10378-06-0
  • Formula Weight
    329.31
  • Molecular Formula
    C14H19NO8
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:100 mg/mL (303.67 mM; Need ultrasonic)
  • SMILES
    CC1=N[C@@]([C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H](COC(C)=O)O2)([H])[C@@]2([H])O1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Francesca Ricciardiello, et al. Inhibition of the Hexosamine Biosynthetic Pathway by Targeting PGM3 Causes Breast Cancer Growth Arrest and Apoptosis. Cell Death Dis. 2018 Mar 7;9(3):377.
molnova catalog
related products
  • GSK854

    GSK854 is a highly selective and potent inhibitor of troponin I interacting kinase (TNNI3K) that inhibits myocardial infarction-injured cellular pyroptosis and apoptosis in mice, which may limit oxidative stress, injury, and adverse remodeling in the ischemic heart.

  • 1-(4-Chloro-3-(trifl...

    SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib. SC-1 potently inhibits the phosphorylation of STAT3 by blocking STAT3 phosphorylation and activation, and induces apoptosis in hepatocellular carcinoma cell lines.

  • Adarotene

    Adarotene is an effective apoptosis inducer. It surprisingly produces DNA damage and exhibits a potent antiproliferative activity on a large panel of human tumor cells.