![](../../files/images/goods/17388-39-5.png)
Swertiamarin
CAS No. 17388-39-5
Swertiamarin ( Swertiamarin | Swertiamaroside )
产品货号. M12637 CAS No. 17388-39-5
Swertiamarin 是一种在 Enicostemma littorale 属植物中发现的裂环烯醚萜苷,具有降血糖和降血脂的作用。
纯度: >98% (HPLC)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥441 | 有现货 |
![]() ![]() |
5MG | ¥688 | 有现货 |
![]() ![]() |
10MG | ¥970 | 有现货 |
![]() ![]() |
25MG | ¥2276 | 有现货 |
![]() ![]() |
100MG | 获取报价 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Swertiamarin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Swertiamarin 是一种在 Enicostemma littorale 属植物中发现的裂环烯醚萜苷,具有降血糖和降血脂的作用。
-
产品描述Extracted from Gentianaceae Swertia L. Swertia mussotii Franch;Suitability:Methanol,ethanol;Store the product in sealed,cool and dry condition.
-
体外实验——
-
体内实验——
-
同义词Swertiamarin | Swertiamaroside
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域Other Indications
-
适应症——
化学信息
-
CAS Number17388-39-5
-
分子量374.34
-
分子式C16H22O10
-
纯度>98% (HPLC)
-
溶解度DMSO: 10 mM
-
SMILESO=C1OCC[C@]2(O)C1=CO[C@@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H]2C=C
-
化学全称(3S,4R,4aR)-4-ethenyl-4a-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydropyrano[3,4-c]pyran-8-one
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Saravanan S, et al. Eur J Pharm Sci. 2014 Jun 2;56:70-86.
产品手册
![](/themes/theme/en/images/ct.png)
![](/themes/theme/en/images/new12.jpg)
![](/themes/theme/en/images/gift.jpg)
![](/themes/theme/en/images/ct2.png)
关联产品
-
Decuroside I
Decuroside I shows weak inhibiting activity against the primary and secondary wave aggregation of human platelet.
-
Bendamustine
苯达莫司汀用于治疗非霍奇金淋巴瘤和慢性淋巴细胞白血病。
-
Allocryptopine
Allocryptopine has certain effects on anti-injury for hepatocyte, ameliorating liver function, and prohibiting hepatic fibrosis; it increases mRNA levels of cytochromes P450 1A in human hepatocytes and HepG2 cells independently of AhR.