VRX-0466617

CAS No. 926906-64-1

VRX-0466617( VRX 0466617 | VRX0466617 )

Catalog No. M16639 CAS No. 926906-64-1

A potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 963 Get Quote
50MG 1962 Get Quote
100MG 2520 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    VRX-0466617
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM).
  • Description
    A potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM); inhibits the phosphorylation of Chk2 Ser(19) and Ser(33-35), but not of Chk2 Thr(68), prevents the IR-induced Chk2-dependent degradation of Hdmx and attenuates IR-induced apoptosis.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    VRX 0466617 | VRX0466617
  • Pathway
    Angiogenesis
  • Target
    Chk
  • Recptor
    Chk
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    926906-64-1
  • Formula Weight
    462.366
  • Molecular Formula
    C19H20BrN5O2S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    N/C(C1=C(NC2=CC=C(NC3=CC=C(Br)C=C3)C=C2)SNC1=O)=N\C(C)CO
  • Chemical Name
    5-[4-(4-Bromoanilino)anilino]-N'-(1-hydroxypropan-2-yl)-3-oxo-1,2-thiazole-4-carboximidamide

Shipping & Storage Information

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

Reference

1. Carlessi L, et al. Mol Cancer Ther. 2007 Mar; 6(3):935-44. 2. Carlessi L, et al. Biochim Biophys Acta. 2010 Oct;1803(10):1213-23.
molnova catalog
related products
  • PV-1019

    A potent, ATP-competitive and highly selective Chk2 inhibitor with IC50 of 138 nM.

  • CCT-245737

    A highly potent, selective, ATP-competitive inhibitor of Chk1 with IC50 of 1.3 nM; weak inhibition on Chk2 (IC50=2440 nM).

  • PHI-101

    PHI-101 is an orally available and selective checkpoint kinase 2 (Chk2) inhibitor for the study of refractory acute myelogenous leukemia (AML) and ovarian cancer.