化合物YM201636 T6110

Product Introduction
Bioactivity


英文名: YM-201636

描述: YM201636 是是一种特异性 PIKfyve 抑制剂，IC50值为 33 nM，对 p110α的IC50为 3.3 μM。它还可抑制逆转录病毒复制。

细胞实验: YM-201636 is dissolved in DMSO and diluted with DMEM and added to cells at a final concentration of 800 nM. Cells are treated with YM-201636 or a DMSO control for 2 h. For TER measurements cells are plated at confluency on Transwell permeable polyester filters (0.4 μM pore size) with surface area of 0.33 cm2. Media is changed ever 2-3 days and cells are grown for 7 days prior to TER measurements[4].

激酶实验: Following 3T3L1 adipocyte serum-starvation and insulin stimulation, cell lysates containing protease inhibitors are clarified and then subjected to immunoprecipitation with anti-PIKfyve antibodies. Washed beads are mixed with 100 μM PtdIns and preincubated for 15 min with YM-201636 (100 nM) or vehicle in the assay buffer (50 mM Tris-HCl, pH 7.5, 1 mM EGTA and 10 mM MgCl2). The kinase assay (50 μL final volume) is carried out for 15 min at 37 °C with 15 μM ATP and [γ-32P]ATP (30 μCi). Lipids are extracted, spotted on TLC glass plates (250 μm), resolved by a chloroform/methanol/water/ammonia solvent system and detected by autoradiography[2].

体内活性: 在血清饥饿处理的NIH3T3细胞中, YM201636（0.8 μM）明显降低PtdIns(3,5)P2产量,降低达 80%。在3T3L1脂肪细胞中,YM-201636（IC50=54 nM）抑制2-脱氧葡萄糖吸收, 按160 nM剂量处理时,则能够完全抑制2-脱氧葡萄糖吸收。在MDCK细胞中,YM201636细胞间隙连接蛋白Claudin-1和Claudin-2的连续再循环,导致细胞内累积,也延迟上皮屏障的形成。

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: Ethanol : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 33 mg/mL (70.6 mM)
H2O : < 1 mg/mL (insoluble or slightly soluble)


关键字: Inhibitor | Fab1 | PI3K | inhibit | YM-201636 | Influenza Virus | PIKfyve | Autophagy | Phosphoinositide 3-kinase | YM201636 | YM 201636

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注：该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案，不可用于临床诊断或治疗等相关用途