WAY-322243

CAS No. 332939-32-9

WAY-322243( —— )

Catalog No. M36995 CAS No. 332939-32-9

WAY-322243 has antibacterial and anti-inflammatory activity and has an inhibitory effect on CLK-1, which can be used to study Alzheimer's disease.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 51 Get Quote
10MG 84 Get Quote
25MG 171 Get Quote
50MG 257 Get Quote
100MG 381 Get Quote
500MG 861 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    WAY-322243
  • Note
    Research use only, not for human use.
  • Brief Description
    WAY-322243 has antibacterial and anti-inflammatory activity and has an inhibitory effect on CLK-1, which can be used to study Alzheimer's disease.
  • Description
    WAY-322243 has antibacterial and anti-inflammatory activity and has an inhibitory effect on CLK-1, which can be used to study Alzheimer's disease.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    CDK
  • Recptor
    CDK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    332939-32-9
  • Formula Weight
    326.41
  • Molecular Formula
    C18H18N2O2S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(NC(CCC)=O)(C1=C(O)C2=C(C=C1)C=CC=N2)C3=CC=CS3
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • PHA-848125

    A potent, selective, brain penetrant and orally available dual CDK and TRK inhibitor with IC50 of 45 and 53 nM for CDK2/cyclin A and TrkA, respectively; shows cross-reactivity with other CDKs (CDK1/4/5/7), TrkB/C, Kit, Abl and PDGFR (IC50s<1 uM).

  • Palbociclib hydrochl...

    A potent and selective inhibitor of CDK4/6 with IC50 of 11 nM/16 nM; no inhibition for CDK2A (IC50>5 uM); inhibits MDA-MB453 cells with IC50 of 0.16 uM.

  • TG003 B

    TG003 is a potent Clk1/Sty inhibitor that inhibits Clk1 and Clk4, inhibits cancer cell growth and induces apoptosis, and can be used in the study of Duchenne muscular dystrophy.