NSC-109555 ditosylate

CAS No. 66748-43-4

NSC-109555 ditosylate( DDUG | NSC109555 | NSC 109555 )

Catalog No. M15549 CAS No. 66748-43-4

A potent, selective, reversible, ATP-competitive Chk2 inhibitor with IC50 of 0.2 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 873 Get Quote
50MG 1782 Get Quote
100MG 2250 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    NSC-109555 ditosylate
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective, reversible, ATP-competitive Chk2 inhibitor with IC50 of 0.2 uM.
  • Description
    A potent, selective, reversible, ATP-competitive Chk2 inhibitor with IC50 of 0.2 uM; displays no effect on a range of other kinases including Chk1 (IC50>10 uM); inhibits histone H1 phosphorylation (IC50=0.24 uM) and attenuates mitochondrial ATP synthesis; exhibits antiproliferative activity in a number of leukemias in vivo.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    DDUG | NSC109555 | NSC 109555
  • Pathway
    Angiogenesis
  • Target
    Chk
  • Recptor
    Chk
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    66748-43-4
  • Formula Weight
    752.86
  • Molecular Formula
    C19H24N10O.2C7H8O3S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(NC1=CC=C(/C(C)=N/N=C(N)/N)C=C1)NC2=CC=C(/C(C)=N/N=C(N)/N)C=C2.OS(=O)(C3=CC=C(C)C=C3)=O.OS(=O)(C4=CC=C(C)C=C4)=O
  • Chemical Name
    4,4'-diacetyldiphenylurea bis(guanylhydrazone) ditosylate

Shipping & Storage Information

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

Reference

1. Jobson AG, et al. Mol Pharmacol. 2007 Oct; 72(4):876-84. 2. Gogineni VR, et al. Cancer Lett. 2011 Dec 26;313(1):64-75. 3. Mikles-Robertson F, et al. Cancer Res. 1980 Apr;40(4):1054-61.
molnova catalog
related products
  • VRX-0466617

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

  • GDC0575 monohydrochl...

    GDC-0575 is a potent and selective inhibitor of cell cycle checkpoint kinase 1 (Chk1) with an IC50 of 1.2?nM. GDC-0575 specifically binds to and inhibits Chk1; this may result in tumor cells bypassing Chk1-dependent cell cycle arrest in the S and G2/M phases, which permits the cells to undergo DNA repair prior to entry into mitosis.

  • Baricitinib

    Baricitinib (LY3009104, INCB028050) is a selective JAK1 and JAK2 inhibitor with IC50 of 5.9 nM and 5.7 nM in cell-free assays.