ML-193 ≥98%
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| 包装规格: | 5mg 25mg 100mg 250mg in glass bottle |
| 产品描述: | 基本信息 产品编号: M11619 产品名称: ML-193 CAS: 713121-80-3 储存条件 粉末 -20℃ 四年 分子式: C28H25N5O4S 溶于液体 -80℃ 二年 分子量: 527.59 化学名: N-(4-(N-(3,4-Dimethylisoxazol-5-yl)sulfamoyl)phenyl)-6,8-dimethyl-2-(pyridin-2-yl)quinoline-4-carboxamide Solubility (25°C): 体外: DMSO Ethanol Water 体内(现配现用): <1mg/ml表示微溶或不溶。 普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 生物活性 产品描述 一种有效和选择性的 GPR55 拮抗剂。 可以改善帕金森氏病 (PD) 大鼠的运动和感觉运动缺陷。 靶点 IC50:221nM (GPR55) 体外研究 ML-193 (0.01-100μM;pretreated for 15 min) inhibits β-arrestin trafficking induced by L-α-lysophophosphatidylinositol (LPI,10μM) and ML186 (1μM) with IC50s of 0.22μM and 0.12μM,respectively.ML-193 (0.01-10μM;pretreated for 30 min) decreases the LPI-mediated ERK1/2 phosphorylation,with an IC50 of 0.2μM in U2OS cells.ML-193 (5μM;pretreated for 30 min) attenuates the GPR55 agonists induced increases in hNSCs proliferation rates.ML-193 (5μM;10 d) attenuates the ML184-induced increases in hNSCs differentiation. 体内研究 ML193 (1 and 5µg/rat;intra-striatal at a rate of 1μL/min) attenuates sensorimotor deficits and slip steps,increases motor coordination in PD rats. Animal Model: Male Wistar rats (200-250g) were induced experimental Parkinson by 6-hydroxydopamine (6-OHDA,10µg/rat) Dosage: 1 and 5µg/rat Administration: Injected into the right striatum at a rate of 1μL/min Result: Increased the time on the rotarod,decreased latency to remove the label and slip steps in 6-OHDA-lesioned rats. |
| 保存条件: | -20℃ |
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