GSK-1

CAS No. 912953-25-4

GSK-1( —— )

Catalog No. M16555 CAS No. 912953-25-4

GSK-1 is an ATP-competitive inhibitor of the mitotic kinesin KSP with HCT116 cell IC50 of 36 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    GSK-1
  • Note
    Research use only, not for human use.
  • Brief Description
    GSK-1 is an ATP-competitive inhibitor of the mitotic kinesin KSP with HCT116 cell IC50 of 36 nM.
  • Description
    GSK-1 is an ATP-competitive inhibitor of the mitotic kinesin KSP with HCT116 cell IC50 of 36 nM; induces monopolar spindle formation in SKOV3 cells, and shows markedly greater potency (IC50 of 0.5 nM) in the ispinesib-resistant HCT116-D130V cell line.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Kinesin
  • Recptor
    Kinesin
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    912953-25-4
  • Formula Weight
    291.273
  • Molecular Formula
    C16H12F3NO
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C1CC(=O)NC2=C1C=C(C=C2)C3=CC=C(C=C3)C(F)(F)F
  • Chemical Name
    6-(4-(trifluoromethyl)phenyl)-3,4-dihydroquinolin-2(1H)-one

Shipping & Storage Information

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

Reference

1. Luo L, et al. Nat Chem Biol. 2007 Nov;3(11):722-6.
molnova catalog
related products
  • WZ8040

    WZ8040 is a novel mutant-selective irreversible EGFRT790M inhibitor, does not inhibit ERBB2 phosphorylation (T798I).

  • TUG-891

    TUG-891 is a G protein-coupled receptor (GPCR) expressed in intestine, adipocytes, and pro-inflammatory macrophages that is activated by long chain free fatty acids.

  • Eg5 Inhibitor V, tra...

    Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 agonist inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.