CIM0216 ≥98%
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| 包装规格: | 5mg in glass bottle |
| 溶解性: | 溶于DMSO(30mg/ml 超声) |
| 产品描述: | 基本信息 产品编号: C11210 产品名称: CIM0216 CAS: 1031496-06-6 储存条件 粉末 -20℃ 四年 分子式: C21H21N3O2 溶于液体 -80℃ 6个月 分子量: 347.41 -20℃ 1个月 化学名: 2-(3,4-Dihydro-1(2H)-quinolinyl)-N-(5-methyl-3-isoxazolyl)-2-phenylacetamide (Adriamycin) 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。 制备储备液 浓度 溶液体积 质量 1mg 5mg 10mg 1mM 2.8784mL 14.3922mL 28.7844mL 5mM 0.5757mL 2.8784mL 5.7569mL 10mM 0.2878mL 1.4392mL 2.8784mL 生物活性 产品描述 一种合成的TRPM3配体,是一种有效的选择性TRPM3激动剂。CIM0216对TRPM3的选择性高于TRPM1、TRPM2和TRPM4-8。CIM0216以TRPM3依赖性的方式引起疼痛并唤起感觉神经末梢的神经肽释放。CIM0216是研究TRPM3生理功能的有力工具,可用于神经源性炎症的相关研究。 靶点 TRPM3 体外研究 CIM0216 elicits a dose-dependent Ca2+ response [pEC50=0.77±0.1µM] in HEK-TRPM3 cells,which is not observed in nontransfected HEK293 cells.CIM0216 induces a robust increase in intracellular Ca2+ concentration (1,145±26nM) in singlecell FURA2-ratiometric Ca2+ imaging in HEK-TRPM3 cells. These responses are not observed in nontransfected HEK cells or in the absence of extracellular Ca2+.CIM0216 (10µM) has no stimulating/blocking effect on TRPM1,TRPM4,TRPM6,or TRPM7 currents;however,a small blocking effect of CIM0216 is observed after activation of TRPM2 (16.6% block) and TRPM5 (33.5% block).CIM0216 also has no detectable effect on human TRPV1 and TRPM8 channel activation. |
| 保存条件: | -20℃ |
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