SCFSkp2-IN-2
CAS No. 1375060-02-8
SCFSkp2-IN-2( —— )
Catalog No. M36410 CAS No. 1375060-02-8
SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM. It demonstrates antitumor activities by inducing apoptosis in non-small cell lung cancer (NSCLC) cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 37 | Get Quote |
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| 10MG | 61 | Get Quote |
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| 25MG | 118 | Get Quote |
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| 50MG | 196 | Get Quote |
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| 100MG | 335 | Get Quote |
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| 500MG | 782 | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameSCFSkp2-IN-2
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NoteResearch use only, not for human use.
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Brief DescriptionSCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM. It demonstrates antitumor activities by inducing apoptosis in non-small cell lung cancer (NSCLC) cells.
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DescriptionSCFSkp2-IN-2 (Compound AAA-237) is a Skp2 inhibitor with a KD of 28.77 μM. AAA-237 induces apoptosis of NSCLC cells and shows antitumor activities.
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In VitroWestern Blot AnalysisCell Line:A549 and H1299 cellsConcentration:0.3, 1 and 3 μMIncubation Time:24, 48 and 72 hResult: Increased the expression levels of p21Cip1 and p27Kip1. Decreased the level of Skp2. Reduced the expression levels of CDK2, p-CDK2, cyclin E1, CDK4, p-CDK4 and cyclin D. Increased the levels of cleaved PARP, cleaved caspase 3, cleaved caspase 9 and Bax. Decreased the expression of PARP and Bcl-2.Cell Proliferation Assay Cell Line:A549 and H1299 cells Concentration:0.3, 1 and 3 μM Incubation Time:24, 48 and 72 h Result:Inhibited the proliferation of A549 and H1299 cells in a dose- and time-dependent manner. The IC50 for A549 was 3?μM at 24?h, 2.5?μM at 48?h and 0.7?μM at 72?h. The IC50 for H1299 was 3.9?μM at 24?h, 1.8?μM at 48?h and 1.1?μM at 72?h.Cell Cycle Analysis Cell Line:A549 and H1299 cells Concentration:0.3, 1 and 3 μM Incubation Time:24, 48 and 72 h Result: Arrested the cell cycle at G0/G1 in a dose- and time-dependent manner. Apoptosis Analysis Cell Line:A549 and H1299 cells Concentration:0.3, 1 and 3 μM Incubation Time:24, 48 and 72 h Result:The ratio of JC-1 monomer/JC-1 polymer was increased in A549 and H1299 cells as the concentration was increased.
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In VivoAnimal Model:A549 xenograft model Dosage:15 or 45?mg/kg Administration:Intraperitoneal administration, daily for 14 days Result:Significantly reduced tumor volume and weight. The tumor growth inhibition of the low dose and high dose was 55% and 64%, respectively. No obvious weight loss or abnormal behavior was observed. Reduced the expression of Ki67 in tumor tissue. Reduced the expression of Skp2 and Bcl-2 and increased the expression of p27, the cleaving of caspase 3, caspase 9, PARP and Bax.
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorApoptosis | E1/E2/E3 Enzyme
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Research Area——
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Indication——
Chemical Information
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CAS Number1375060-02-8
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Formula Weight312.37
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Molecular FormulaC17H20N4O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (400.17 mM; Ultrasonic (<60°C)
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SMILESN(CC)(CC)C1=CC(O)=C(/C=N/NC(=O)C=2C=CC=NC2)C=C1
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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
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ZDLD20
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DT2216
DT2216 inhibits various Bcl-XL-dependent leukemias and cancer cells, but is significantly less toxic to platelets.DT2216 is a selective B-cell lymphoma, extremely large (BCL-XL), proteolytic targeting chimera (PROTAC).
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Merodantoin
Merodantoin is an apoptosis inducer and triggers cell apoptosis associated with ROS-dependent autophagy. Merodantoin targets cancer cells expressing KRAS mutations involved in Akt-dependent ROS production.
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