SR-31747 ≥98%
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| 包装规格: | 1mg 5mg 10mg in glass bottle |
| 溶解性: | 溶于DMSO(15mg/mL超声) |
| 产品描述: | 基本信息 产品编号: S11209 产品名称: SR-31747 CAS: 132173-07-0 储存条件 粉末 -20℃ 四年 分子式: C23H35Cl2N 溶于液体 -80℃ 6个月 分子量 396.44 -20℃ 1个月 化学名: N-Cyclohexyl-N-ethyl-3-(3-chloro-4-cyclohexylphenyl)propen-2-ylamine hydrochloride 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 2.5224mL 12.6122mL 25.2245mL 5mM 0.5045mL 2.5224mL 5.0449mL 10mM 0.2522mL 1.2612mL 2.5224mL 生物活性 产品描述 一种具有免疫抑制和抗炎特性的 sigma 配体。SR-31747 通过抑制固醇异构酶来阻止细胞增殖。 靶点 Sigma ligand 体外研究 SR-31747 blocks the proliferation of lymphocytes at a concentration of 10nM.SR-31747 is capable of inhibiting T-cell proliferation when added as late as 24h after activation.SR-31747 arrests proliferation in yeast cells in a dose-dependent manner. 体内研究 In vivo,SR-31747 dramatically blocks lipopolysaccharide-induced production of IL-1,IL-6 and TNF-α in a dose-dependent manner (ED50,2mg/kg).SR-31747 probably abrogated monokine production through an indirect mechanism that involves endogenous corticosteroids.This conclusion was supported by in vivo experiments that shows that:1) ablation of corticosteroids by use of Mifepristone or adrenalectomy suppress the effect of SR-31747;2) administration of SR-31747 induces an enhancement of the corticosterone level.SR-31747 improves the survival of animals with endotoxinic shock as a result of monokine inhibition. |
| 保存条件: | -20℃ |
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