(E)-Ligustilide

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
(E)-Ligustilide 

(E)-Ligustilide 是从当归中分离得到的,具有肾脏保护作用。

(E)-Ligustilide

(E)-Ligustilide Chemical Structure

CAS No. : 81944-08-3

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(E)-Ligustilide 相关产品

同靶点产品:

同靶点蛋白产品:

生物活性

(E)-Ligustilide is isolated from Angelica sinensis and has nephroprotective effects[1].

体外研究
(In Vitro)

(E)-Ligustilide (50 μM; 24-72 hours) decreases HK-2 cell survival to 86%, to 67% and to 49% for 24, 48 or 72 hours incubation, respectively[1].
(E)-Ligustilide (50 μM; 48-72 hours) alone decreases the metabolic activity to 87±6% and 71±8% after 48 and 72 h incubation, respectively, as compared to the control condition in HK-2 cells[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

(E)-Ligustilide 相关抗体:

Cell Viability Assay[1]

Cell Line: HK-2 cell
Concentration: 50 μM
Incubation Time: 24 hours, 48 hours and 72 hours
Result: Decreased cell survival as a dose-dependent manner.

分子量

190.24

Formula

C12H14O2

CAS 号

81944-08-3

结构分类
  • Others
初始来源
  • 植物
  • 菊科
  • Echinacea angustifolia DC.
  • 植物
  • 伞形科
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
Data Sheet (526 KB) 产品使用指南 (1538 KB)

参考文献
  • [1]. Bunel V, et al. Nephroprotective effects of ferulic acid, Z-ligustilide and E-ligustilide isolated from Angelica sinensis against cisplatin toxicity in vitro.Toxicol In Vitro. 2015 Apr;29(3):458-67.  [Content Brief]

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