目录:MedChemExpress LLC>>生化试剂>> ISA-2011B | MCE
CAS | 1395347-24-6 | 纯度 | 99.94% |
---|---|---|---|
分子量 | 423.85 | 分子式 | C₂₂H₁₈ClN₃O₄ |
供货周期 | 现货 | 规格 | 1 mg |
货号 | HY-16937 | 应用领域 | 医疗卫生,化工,生物产业,制药/生物制药 |
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CAS No. : 1395347-24-6
产品活性:ISA-2011B is a PIP5K1α inhibitor with promising anticancer effects .
研究领域:Others
作用靶点:Others
In Vitro: The proliferation rate of PC-3 cells after treatment with ISA-2011B at 10, 20, and 50 μM is significantly reduced to 58.77%, 48.65%, and 21.62% of vehicle-treated controls, respectively. ISA-2011B exhibits the highest binding affinity to PIP5K1α, and to MAP/microtubule affinity-regulating kinase 1 and 4 (MARK1 and MARK4) across 460 kinases. ISA-2011B treatment inhibits PIP5K1α expression by 78.6% in PC-3 cells. ISA-2011B leads to a remarkable reduction in AR-V7 and CDK1 in both nucleus and cytoplasm of 22Rv1 cells. ISA-2011B treatment also abolishes AR expression in the nucleus, without depleting the cytoplasmic AR.
In Vivo: ISA-2011B significantly inhibits growth of tumor cells in xenograft mice, and is mediated by targeting PIP5K1α-associated PI3K/AKT and the downstream survival, proliferation, and invasion pathways. Overexpression of AR-V7 increases PIP5K1α, promotes rapid growth of PCa in xenograft mice, whereas inhibition of PIP5K1α by its inhibitor ISA-2011B suppresses the growth and invasiveness of xenograft tumors overexpressing AR-V7. ISA-2011B disrupts protein stabilization of AR-V7 which is dependent on PIP5K1α, leading to suppression of invasive growth of AR-V7-high tumors in xenograft mice.
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