CHM-1

CAS No. 154554-41-3

CHM-1( NSC656158 )

Catalog No. M27612 CAS No. 154554-41-3

CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    CHM-1
  • Note
    Research use only, not for human use.
  • Brief Description
    CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.
  • Description
    CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.(In Vitro):CHM-1 (0-10 μM; 24 hours) significantly increased the binding of cyclin B1 to Cdc2 and induced change in expressed and phosphorylated status of G2-M regulators in HA22T cells. CHM-1 (0-100μM; 24 hours) induced significant concentration-dependent growth inhibition in HA22T, Hep3B, and HepG2 cells, with the most potent effects observed in HA22T cells with an IC50 of 0.75 μM).(In Vivo):In male severe combined immunodeficient mice, CHM-1 (10 mg/kg; i.p.) induced inhibition of HA22T tumor growth in a dose-dependent manner.
  • In Vitro
    CHM-1 (0-100μM; 24 hours) induces significant concentration-dependent growth inhibition in HA22T, Hep3B, and HepG2 cells, with the most potent effects observed in HA22T cells (IC50 = 0.75 μM).CHM-1 (0-10 μM; 24 hours) significantly increases the binding of cyclin B1 to Cdc2 in HA22T cells. Cell Viability Assay Cell Line:HA22T, Hep3B, and HepG2 cells Concentration:0-100 μM Incubation Time:24 hours Result:Induced G2-M arrest of the cell cycle followed by apoptosis.Western Blot Analysis Cell Line:HA22T cells Concentration:0-10 μM Incubation Time:24 hours Result:Induced change in expressed and phosphorylated status of G2-M regulators in human hepatocellular carcinoma cells.
  • In Vivo
    CHM-1 (10 mg/kg; I.p.) induces a dose-dependent inhibition of HA22T tumor growth. Animal Model:Male severe combined immunodeficient mice (HA22T)Dosage:10 mg/kg Administration:I.p.Result:Induced a dose-dependent inhibition of HA22T tumor growth.
  • Synonyms
    NSC656158
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    Antibiotic|P-glycoprotein
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    154554-41-3
  • Formula Weight
    283.258
  • Molecular Formula
    C16H10FNO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 5 mg/mL (17.65 mM)
  • SMILES
    Fc1ccccc1-c1cc(=O)c2cc3OCOc3cc2[nH]1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Phung-Ba V et al. Interaction of pristinamycin IA with P-glycoprotein in human intestinal epithelial cells. Eur J Pharmacol. 1995 Jan 16;288(2):187-92.
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