TG003

CAS No. 300801-52-9

TG003( —— )

Catalog No. M13931 CAS No. 300801-52-9

TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor with IC50 of 20 nM, 200 nM, and 15 nM for Clk1, Clk2, and Clk4, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 46 In Stock
2MG 33 In Stock
5MG 46 In Stock
10MG 80 In Stock
25MG 159 In Stock
50MG 266 In Stock
100MG 390 In Stock
200MG 554 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    TG003
  • Note
    Research use only, not for human use.
  • Brief Description
    TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor with IC50 of 20 nM, 200 nM, and 15 nM for Clk1, Clk2, and Clk4, respectively.
  • Description
    TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor with IC50 of 20 nM, 200 nM, and 15 nM for Clk1, Clk2, and Clk4, respectively. No inhibitory effect on Clk3, SRPK1, SRPK2, or PKC.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    Bcl-2
  • Recptor
    mCLK1| mCLK2| mCLK4
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    300801-52-9
  • Formula Weight
    249.33
  • Molecular Formula
    C13H15NO2S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 6 mg/mL warmed (24.06 mM)
  • SMILES
    CCN\1C2=C(C=CC(=C2)OC)S/C1=C\C(=O)C
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Muraki M, et al. J Biol Chem. 2004, 279(23), 24246-24254.
molnova catalog
related products
  • trans-Ferulic acid

    Trans-Ferulic acid causes the phosphorylation of β-catenin resulting in proteasomal degradation of β-catenin and increases the expression of pro-apoptotic factor Bax and decreases the expression of pro-survival factor survivin.trans-Ferulic acid exert both anti-proliferation and anti-migration effects in the human lung cancer cell line H1299.

  • BTSA1

    BTSA1 is a BAX activator that binds with high affinity and specificity to the N-terminal activation site and induces conformational changes to BAX leading to BAX-mediated apoptosis.

  • S-63845

    S-63845 (S63845)?is a highly potent, selective Mcl-1 inhibitor with Kd of 0.19 nM.