
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)






Size | Price / USD | Stock | Quantity |
2MG | 296 | Get Quote |
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5MG | 459 | Get Quote |
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10MG | 657 | Get Quote |
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25MG | 994 | Get Quote |
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50MG | 1371 | Get Quote |
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100MG | 1773 | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameSkp2 inhibitor 1
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NoteResearch use only, not for human use.
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Brief DescriptionSkp2 inhibitor 1 is a Skp2-Cks1 interaction inhibitor (IC50: 2.8μM) with antitumor activity and can be used to study cancer.
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DescriptionSkp2 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.
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In VitroCell 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.
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In VivoAnimal 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.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number2760612-63-1
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Formula Weight406.91
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Molecular FormulaC23H23ClN4O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (122.88 mM; Ultrasonic )
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SMILESO=C(NC1CCN(C2=NC(C3=CC=CC=C3)=C(N=C2)C=4C=CC=CC4)CC1)CCl
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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. 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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