LY-364947

CAS No. 396129-53-6

LY-364947( HTS 466284 | TGF-β RI Kinase Inhibitor )

Catalog No. M14364 CAS No. 396129-53-6

LY364947 is a potent ATP-competitive inhibitor of TGFβR-I with IC50 of 59 nM in a cell-free assay, shows 7-fold selectivity over TGFβR-II.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 53 In Stock
10MG 68 In Stock
25MG 131 In Stock
50MG 241 In Stock
100MG 354 In Stock
200MG 530 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LY-364947
  • Note
    Research use only, not for human use.
  • Brief Description
    LY364947 is a potent ATP-competitive inhibitor of TGFβR-I with IC50 of 59 nM in a cell-free assay, shows 7-fold selectivity over TGFβR-II.
  • Description
    LY364947 is a potent ATP-competitive inhibitor of TGFβR-I with IC50 of 59 nM in a cell-free assay, shows 7-fold selectivity over TGFβR-II.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    HTS 466284 | TGF-β RI Kinase Inhibitor
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Casein Kinase
  • Recptor
    CK1δ| MLK-7K| TGFβRI| TGFβRII| RIPK2
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    396129-53-6
  • Formula Weight
    272.3
  • Molecular Formula
    C17H12N4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 1 mg/mL (3.67 mM)
  • SMILES
    C1(C2=CNN=C2C3=NC=CC=C3)=CC=NC4=CC=CC=C14
  • Chemical Name
    4-(3-(pyridin-2-yl)-1H-pyrazol-4-yl)quinoline

Shipping & Storage Information

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

Reference

1. Li HY, et al. J Med Chem, 2006, 49(6), 2138-2142.
molnova catalog
related products
  • Pyrvinium pamoate

    An anthelmintic effective agent for pinworms that shows to be a potent inhibitor of Wnt signaling with EC50 of 10 nM.

  • SSTC3

    SSTC3 is a novel small-molecule CK1α activator with EC50 of 30 nM (WNT-driven reporter gene assay), Kd of 32 nM.

  • TTP 22

    TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/Ki of 0.1 uM/40 nM.