α-​Chaconine (Synonyms: 阿尔法卡茄碱)

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。
α-​Chaconine  (Synonyms: 阿尔法卡茄碱) 纯度: 99.04%

α-Chaconine 可在转录水平抑制 COX-2IL-1βIL-6TNF-α 表达。α-Chaconine 作用于 RAW 264.7 巨噬细胞,在蛋白和 mRNA 水平上抑制 LPS 诱导的 iNOSCOX-2 表达及其启动子活性。α-Chaconine 具有抗炎作用。

α-​Chaconine                                          (Synonyms: 阿尔法卡茄碱)

α-​Chaconine Chemical Structure

CAS No. : 20562-03-2

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α-​Chaconine 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus

同靶点产品:

同靶点蛋白产品:

生物活性

α-Chaconine inhibits the expressions of COX-2, IL-1β, IL-6, and TNF-α at the transcriptional level. α-Chaconine inhibits the LPS-induced expressions of iNOS and COX-2 at the protein and mRNA levels and their promoter activities in RAW 264.7 macrophages. Anti-inflammatory effects[1].

IC50 & Target

COX-2

 

体外研究
(In Vitro)

α-Chaconine attenuates the transcriptional activity of activator protein-1 (AP-1) by reducing the translocation and phosphorylation of c-Jun.α-Chaconine suppresses lipopolysaccharide-induced pro-inflammatory mediators via AP-1 inactivation in RAW 264.7 macrophages and protects mice from endotoxin shock.α-Chaconine also suppresses the phosphorylation of TGF-β-activated kinase-1 (TAK1), which lies upstream of MKK7/JNK signaling[1].

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

α-​Chaconine 相关抗体:

分子量

852.06

Formula

C45H73NO14

CAS 号

20562-03-2

性状

固体

颜色

White to off-white

中文名称

阿尔法卡茄碱

结构分类
  • Alkaloids
  • Pyrrole Alkaloids
  • Alkaloids
  • Piperidine Alkaloids
初始来源
  • 植物
  • 禾本科
  • 玉米
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

纯度 & 产品资料

纯度: 99.04%

Data Sheet (531 KB) SDS (252 KB)

COA (271 KB) HNMR (123 KB) RP-HPLC (213 KB)

产品使用指南 (1538 KB)

参考文献
  • [1]. Lee KG, et al. α-Chaconine isolated from a Solanum tuberosum L. cv Jayoung suppresses lipopolysaccharide-induced pro-inflammatory mediators via AP-1 inactivation in RAW 264.7 macrophages and protects mice from endotoxin shock. Chem Biol Interact. 2  [Content Brief]

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