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Dehydroevodiamine (Synonyms: 去氢吴茱萸碱) 纯度: 99.96%
Dehydroevodiamine 是从吴茱萸 Evodiae Fructus 中分离出的喹唑啉生物碱,对豚鼠心室肌细胞具有抗心律失常作用。Dehydroevodiamine 抑制 LPS 诱导的小鼠巨噬细胞中 iNOS,COX-2,PGE2 和 NF-κB 的表达。
Dehydroevodiamine Chemical Structure
CAS No. : 67909-49-3
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5 mg | ¥450 | In-stock | |
10 mg | ¥600 | In-stock | |
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Dehydroevodiamine 相关产品
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生物活性 |
Dehydroevodiamine is a major bioactive quinazoline alkaloid isolated from Evodiae Fructus, has an antiarrhythmic effect in guinea-pig ventricular myocytes[1]. Dehydroevodiamine inhibits LPS-induced iNOS, COX-2, prostaglandin E2 (PGE2) and nuclear factor-kappa B (NF-κB) expression in murine macrophage cells[2]. |
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IC50 & Target |
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体外研究 (In Vitro) |
Dehydroevodiamine (0-50 μM; 2 hours) inhibits iNOS and COX-2 expression and prevents degradation of IκB-α in LPS induced RAW 264.7 macrophages[2]. Dehydroevodiamine (0-50 μM; 2 hours) inhibits a LPS-induced increase in the iNOS and COX-2 mRNA expression[2]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot Analysis[2]
RT-PCR[2]
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分子量 |
301.34 |
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Formula |
C19H15N3O |
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CAS 号 |
67909-49-3 |
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性状 |
固体 |
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颜色 |
Light yellow to yellow |
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中文名称 |
去氢吴茱萸碱 |
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结构分类 |
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初始来源 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:
DMSO 中的溶解度 : 8.33 mg/mL (27.64 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO) 配制储备液
查看完整储备液配制表
* 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。
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
Concentration (start) × Volume (start) = Concentration (final) × Volume (final) This equation is commonly abbreviated as: C1V1 = C2V2
动物溶解方案计算器
请输入动物实验的基本信息:
给药剂量 mg/kg 动物的平均体重 g 每只动物的给药体积 μL 动物数量 只 由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
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纯度 & 产品资料 |
纯度: 99.96%
Data Sheet (605 KB) SDS (393 KB)
COA (198 KB) HNMR (105 KB) RP-HPLC (102 KB) 产品使用指南 (1538 KB) |
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参考文献 |
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