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Cyclovirobuxine D (Synonyms: 黄杨碱) 纯度: ≥98.0%
Cyclovirobuxine D (CVB-D) 是中药黄杨 Buxus microphylla 的主要活性成分。Cyclovirobuxine D 诱导自噬并减弱 Akt 和 mTOR 的磷酸化。Cyclovirobuxine D 通过抑制细胞周期进程和诱导线粒体介导的细胞凋亡 apoptosis 抑制癌细胞的增殖。Cyclovirobuxine D 有潜力用于心肌梗死引起的心力衰竭的研究。

Cyclovirobuxine D Chemical Structure
CAS No. : 860-79-7
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in Ethanol | ¥440 | In-stock | |
5 mg | ¥400 | In-stock | |
10 mg | ¥700 | In-stock | |
25 mg | ¥1500 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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Cyclovirobuxine D 相关产品
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生物活性 |
Cyclovirobuxine D (CVB-D) is the main active component of the traditional Chinese medicine Buxus microphylla. Cyclovirobuxine D induces autophagy and attenuates the phosphorylation of Akt and mTOR[1]. Cyclovirobuxine D inhibits cell proliferation of gastric cancer cells through suppression of cell cycle progression and inducement of mitochondria-mediated apoptosis[2]. Cyclovirobuxine D is beneficial for heart failure induced by myocardial infarction[3]. |
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体外研究 (In Vitro) |
Cyclovirobuxine D (0-240 µM ;24-72 hours) shows a concentration- and time-dependent reduced cell viability after CVB-D treatment, only 10% MGC-803 cells and 20% MKN28 cells are alive at 72 h after treatment with 240 µM[2]. Cyclovirobuxine D (0-120 µM; 48 hours) arrests the cell cycle of gastric cancer cells at S phase in a concentration-dependent manner[2]. Cyclovirobuxine D (0-120 µM; 48 hours) leads to apoptosis in gastric cancer cells in a concentration-dependent manner, especially early stage apoptosis. Cyclovirobuxine D (0-120 µM; 48 hours) causes apoptosis via up-regulation of the apoptosis- related proteins, cleaved Caspase-3 and ratio of Bax/Bcl-2, in gastric cancer cells[2]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay[2]
Cell Cycle Analysis[2]
Apoptosis Analysis[2]
Western Blot Analysis[2]
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分子量 |
402.66 |
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Formula |
C26H46N2O |
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CAS 号 |
860-79-7 |
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性状 |
固体 |
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颜色 |
White to off-white |
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中文名称 |
黄杨碱 |
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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 |
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溶解性数据 |
In Vitro:
Ethanol 中的溶解度 : 13 mg/mL (32.29 mM; 超声助溶) 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
In Vivo:
请根据您的 实验动物和给药方式 选择适当的溶解方案。 以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
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 (631 KB) SDS (251 KB)
COA (197 KB) HNMR (257 KB) 产品使用指南 (1538 KB) |
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参考文献 |
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