
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)






Size | Price / USD | Stock | Quantity |
2MG | 73 | Get Quote |
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5MG | 120 | Get Quote |
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10MG | 200 | Get Quote |
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25MG | 430 | Get Quote |
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50MG | 617 | Get Quote |
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100MG | 897 | Get Quote |
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500MG | 1791 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameCHM-1
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NoteResearch use only, not for human use.
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Brief DescriptionCHM-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.
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DescriptionCHM-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.
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In VitroCHM-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.
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In VivoCHM-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.
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SynonymsNSC656158
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PathwayApoptosis
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TargetApoptosis
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RecptorAntibiotic|P-glycoprotein
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Research Area——
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Indication——
Chemical Information
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CAS Number154554-41-3
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Formula Weight283.258
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Molecular FormulaC16H10FNO3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 5 mg/mL (17.65 mM)
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SMILESFc1ccccc1-c1cc(=O)c2cc3OCOc3cc2[nH]1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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