
Scopolin
CAS No. 531-44-2
Scopolin ( Scopolin | Murrayin | Scopoloside )
产品货号. M18746 CAS No. 531-44-2
Scopolin 可通过抑制炎症和血管生成来减轻大鼠 AIA 的临床症状,该化合物可能是治疗血管生成相关疾病的有效化合物,并可作为筛选更有效的合成类似物的结构基础。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
10MG | ¥1896 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Scopolin
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Scopolin 可通过抑制炎症和血管生成来减轻大鼠 AIA 的临床症状,该化合物可能是治疗血管生成相关疾病的有效化合物,并可作为筛选更有效的合成类似物的结构基础。
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产品描述Scopolin formation is increased by the enhanced activity of PAL. Scopolin can reduce the clinical symptoms of rat AIA by inhibiting inflammation and angiogenesis, and this compound may be a potent agent for angiogenesis related diseases and can serve as a structural base for screening more potent synthetic analogs.
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体外实验——
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体内实验Animal Model:HFD-fed C57BL/6?N miceDosage:0.02% (w/w) in HFD diet (equivalent to 20?mg/kg body weight)Administration:Supplemented in diet, 8 weeks Result:Reversed the HFD-induced hepatic TG, cholesterol, and fatty acid accumulation by 35%, 49%, and 35%, respectively.Reversed the HFD-induced decrease in plasma adiponectin levels by 76%, and reduced the increased plasma MCP-1, TNFα, and IL-6 levels.Restored HFD-induced downregulation of SIRT1 activity.Animal Model:Adjuvant-induced arthritis (AIA) rats Dosage:50, 100 mg/kg Administration:i.p.Result:Inhibited inoculated and non-inoculated paw swelling and articular index scores.Reduced new blood vessels, and reduced IL-6, VEGF and FGF-2 expressions in rat synovial tissues.
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同义词Scopolin | Murrayin | Scopoloside
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通路Apoptosis
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靶点NF-κB
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受体Others
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研究领域Inflammation/Immunology
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适应症——
化学信息
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CAS Number531-44-2
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分子量354.31
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分子式C16H18O9
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (282.24 mM)
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SMILESCOc1c(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)cc2oc(=O)ccc2c1
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化学全称6-methoxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Pan R,et al. Scopolin isolated from Erycibe obtusifolia Benth stems suppresses adjuvant-induced rat arthritis by inhibiting inflammation and angiogenesis. Int Immunopharmacol. 2009 Jul;9(7-8):859-69.
产品手册




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