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PIP4K-IN-a131
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
PIP4K-IN-a131图片
规格:98%
分子量:295.34
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
PIP4K-IN-a131 是一种脂质激酶 PIP4K 抑制剂,对 PIP4K2A 和 PIP4Ks 作用的 IC50 值分别为 1.9 µM 和 0.6 µM。PIP4K-IN-a131 通过脂质激酶 PIP4Ks 和有丝分裂途径的双阻断选择性杀伤癌细胞。
货号:ajcx29590
CAS:2055405-95-1
分子式:C20H13N3
分子量:295.34
溶解度:N/A
纯度:98%
存储:Store at -20°C
库存:现货

Background:

PIP4K-IN-a131 is PIP4K lipid kinases inhibitor, with IC50s of 1.9 µM and 0.6 µM for purified PIP4K2A and PIP4Ks, respectively. PIP4K-IN-a131 exhibits cancer-selective lethality via dual blockade of the lipid kinase PIP4Ks and mitotic pathways[1].

PIP4K-IN-a131 (0-100 μM; 72 hours) is a potent antiproliferative agent with a clear selectivity toward cancer cells killing[1].PIP4K-IN-a131 eliminates cancer cells via a dual-inhibitory mechanism[1].PIP4K-IN-a131 causes inhibition of the PI3K/Akt/mTOR pathway only in normal BJ cells, but not in transformed counterparts[1].Inhibition of PIP4Ks by PIP4K-IN-a131 arrests normal cells at the G1/S phase of the cell cycle by suppressing the PI3K/Akt/mTOR signaling pathway via transcriptional upregulation of PIK3IP1[1]. Cell Proliferation Assay[1] Cell Line: Normal and transformed BJ cells


[1]. Mayumi Kitagawa, et al. Dual Blockade of the Lipid Kinase PIP4Ks and Mitotic Pathways Leads to Cancer-Selective Lethality. Nat Commun. 2017 Dec 19;8(1):2200.