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
Size Price / USD Stock Quantity
2MG 296 Get Quote
5MG 459 Get Quote
10MG 657 Get Quote
25MG 994 Get Quote
50MG 1371 Get Quote
100MG 1773 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

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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