Skp2 inhibitor 1

CAS No. 2760612-63-1

Skp2 inhibitor 1( —— )

Catalog No. M37593 CAS No. 2760612-63-1

Skp2 inhibitor 1 is a Skp2-Cks1 interaction inhibitor (IC50: 2.8μM) with antitumor activity and can be used to study cancer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Skp2 inhibitor 1
  • Note
    Research use only, not for human use.
  • Brief Description
    Skp2 inhibitor 1 is a Skp2-Cks1 interaction inhibitor (IC50: 2.8μM) with antitumor activity and can be used to study cancer.
  • Description
    Skp2 inhibitor 1 (compound 14i) is a potent and selective Skp2 inhibitor against the Skp2-Cks1 interaction with an IC50 of 2.8 μM. Skp inhibitor 1 exhibits anticancer activity.
  • In Vitro
    Cell Viability Assay Cell Line:PC-3 , MGC-803 Concentration:0-10 μM Incubation Time:72 h Result:Against the Skp2?Cks1 interaction with an IC50 value of 2.8 μM, and against PC-3 and MGC-803 cells with IC50 values of 4.8 and 7.0 μM, respectively. Apoptosis Analysis Cell Line:PC-3 , MGC-803 Concentration:2.5 μM , 5 μM , 10 μM Incubation Time:0-48 h Result:Leaded to cell cycle S-phase arrest in a dose-dependent manner, and induced apoptosis in a dose-dependent manner, such as nuclear fragmentation, condensation, and cell shrinkage.Cell Proliferation Assay Cell Line:PC-3 , MGC-803 Concentration:0.5 μM , 1 μM , 2 μM Incubation Time:10 days Result:Inhibited colony-forming abilities in a dose-dependent manner.Cell Migration Assay Cell Line:PC-3 , MGC-803 Concentration:2.5 μM , 5 μM , 10 μM Incubation Time:48 h Result:Inhibited migration in a dose-dependent manner.Cell Invasion Assay Cell Line:PC-3 , MGC-803 Concentration:0.5 μM , 1 μM , 2 μM Incubation Time:48 h Result:Inhibited invasion in a dose-dependent manner.Western Blot Analysis Cell Line:PC-3 , MGC-803 Concentration:2.5 μM , 5 μM , 10 μM Incubation Time:0-48 h Result:Inhibited the protein levels of Skp2 in a dose-dependent manner, restored the expression of p21 and p27 in a time-dependent manner.
  • In Vivo
    Animal Model:The xenograft models of PC-3 and MGC-803 cells in NOD-SCID mice.Dosage:10 mg/kg; 25 mg/kg, 50 mg/kg Administration:Intraperitoneal injection (i.p.) Result:Inhibited tumor growth without obvious toxicity, the tumor growth inhibition ratio was 55.68, 71.86, and 90.42% with 10, 25, and 50 mg/Kg/2 day, respectively.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2760612-63-1
  • Formula Weight
    406.91
  • Molecular Formula
    C23H23ClN4O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (122.88 mM; Ultrasonic )
  • SMILES
    O=C(NC1CCN(C2=NC(C3=CC=CC=C3)=C(N=C2)C=4C=CC=CC4)CC1)CCl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Zhang K, et al. Discovery of Novel 1,3-Diphenylpyrazine Derivatives as Potent S-Phase Kinase-Associated Protein 2 (Skp2) Inhibitors for the Treatment of Cancer. J Med Chem. 2023 Jun 8;66(11):7221-7242.?
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