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Virodhamine 纯度: ≥98.0%
Virodhamine 是一种内源性大麻素,它通过激活大麻素 (CB) 受体调节神经传递。Virodhamine 是 CB1 受体的拮抗剂和 CB2 受体的激动剂。Virodhamine 通过触发 MAPK 信号和 ROS 的产生诱导巨核细胞分化。 Virodhamine 可用于治疗各种神经疾病,如阿尔茨海默病和帕金森。

Virodhamine Chemical Structure
CAS No. : 287937-12-6
规格 | 价格 | 是否有货 | 数量 |
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5 mg | ¥850 | In-stock | |
10 mg | ¥1450 | In-stock | |
25 mg | ¥3000 | In-stock | |
50 mg | ¥4850 | In-stock | |
100 mg | ¥7800 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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Virodhamine 相关产品
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- Membrane Protein-targeted Compound Library
- Membrane Receptor-targeted Compound Library
生物活性 |
Virodhamine is an endocannabinoid, it regulates neurotransmission by activating the cannabinoid (CB) receptors. Virodhamine is an antagonist of CB1 receptor and an agonist of CB2 receptor. Virodhamine induces megakaryocytic differentiation by triggering MAPK signaling and ROS production. Virodhamine can be used for the research of various neurological disorders such as Alzheimer’s and Parkinson’s diseases[1][2]. |
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体外研究 (In Vitro) |
Virodhamine (50 nM; 72 h) increases adherence, membrane expansion and the size of nucleus[1]. Virodhamine (10-40 μM; 72 h) increases the expression level of CD61 and TRPV1[1]. Virodhamine (72 h) inhibits the cell proliferation of megakaryocyte cells and significantly increases the portion of high ploidy cells as compared to control[1]. Virodhamine significantly increases the protein expression level of CB2 receptorn, ROS production and NAPDH oxidase NOX4 expression in megakaryocytic cells[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. RT-PCR[1]
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体内研究 (In Vivo) |
Virodhamine (1-10 mg/kg; i.p. once) repairs the nicotine (0.8 mg/kg) and immobilization stress induced anxiety in vivo[2]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
347.53 |
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Formula |
C22H37NO2 |
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CAS 号 |
287937-12-6 |
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性状 |
粘稠液体 |
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颜色 |
Yellow to brown |
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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 |
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溶解性数据 |
In Vitro:
DMSO 中的溶解度 : ≥ 100 mg/mL (287.74 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO) * “≥” means soluble, but saturation unknown. 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: ≥98.0%
Data Sheet (598 KB) SDS (251 KB)
COA (159 KB) HNMR (249 KB) MS (176 KB) 产品使用指南 (1538 KB) |
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参考文献 |
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