NPD15261
NPD15261 (MI102) is a highly selective MYCN inhibitor. NPD15261 reduces the mRNA and protein levels of MYCN in liver cancer cells, inhibits cell proliferation and colony formation, and induces Apoptosis simultaneously. NPD15261 can be used in liver cancer research.
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- CAS 番号: 895901-42-5
- 分子式: C28H32N2O5
- 分子量:476.56
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
NPD15261 (0-10 μM; 2 h) inhibits basal and HGF-induced phosphorylation of MET at Y1234/Y1235 in JHH7 cells with an IC50 of 0.77 μM, and also suppresses HGF-induced MET phosphorylation at Y1349[1].
NPD15261 (0-10 μM) dose-dependently inhibits the expression of MYCN mRNA and protein in JHH7 cells, and this effect can be partially reversed by stimulation with 20 ng/mL HGF[1].
NPD15261 (0-5 μM; 4 days) selectively reduces the viability of JHH7 cells and the survival rate of JHH7 spheroids at the concentration of 5 μM, with no effect on normal Hc cells[1].
NPD15261 (2.5-10 μM; 0-12 days) inhibits colony formation of JHH7 cells and exerts a dose-dependent inhibitory effect on the proliferation of JHH7 cells[1].
NPD15261 (2.5 μM; 24 h) induces apoptosis in JHH7 cells, while exhibiting extremely low cytotoxicity against normal Hc cells[1].
NPD15261 (5-10 μM; 6 h) downregulates MYCN-related oncogenic pathways (including MYC_Targets_V2, MYC_Targets_V1 and E2F_Targets), and selectively inhibits MYCN target genes in JHH7 cells after 6 hours of treatment, with no effect on normal Hc cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:JHH7 cells
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Concentration:0, 0.5, 1, 2.5, 5, 10 μM , with or without HGF (10 ng/mL)
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Incubation Time:2 h
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Result:Inhibited the phosphorylation of MET at Y1234/Y1235 as well as HGF-induced phosphorylation at Y1234/Y1235 and Y1349 in a dose-dependent manner.
Inhibited MET phosphorylation at Y1234/Y1235 by approximately 83% at 1 μM, with an estimated IC50 value
of 0.77 μM.
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Cell Line:human hepatocellular carcinoma JHH7 cells, normal hepatic Hc cells
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Concentration:0, 0.2, 1, 5 μM
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Incubation Time:4 days
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Result:Markedly reduced JHH7 cell viability at 5 μM.
Showed no observable effects on normal hepatic Hc cells.
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Cell Line:human hepatocellular carcinoma JHH7 cells, normal hepatic Hc cells
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Concentration:2.5 μM
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Incubation Time:24 h
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Result:Induced apoptosis in JHH7 cells.
Showed no significant cytotoxicity to normal hepatic Hc cells.
化学情報
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CAS 番号 895901-42-5
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分子量 476.56
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分子式 C28H32N2O5
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SMILES
CNC1CCC2=C(C(OC)=C(OC)C(OC)=C2)C(C1=C3)=CC=C(NCC4=C(OC)C=CC=C4)C3=O
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別名
MI102
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)