Shikimic acid
(Synonyms: 莽草酸) 目录号 : GN10622
A cyclohexenecarboxylic acid
Cas No.:138-59-0
Sample solution is provided at 25 µL, 10mM.
;)
,-1-7$$$37316672.jpg');)
;)
;)
$$$36806353.jpg');)
;33(7)%EF%BC%9A546-561$$$37156877.jpg');)
;)
;)
;)
%201124-1138.$$$35908550.jpg');)
%20766-780.$$$37100057.jpg');)
%20418-432.$$$36893736.jpg');)
%EF%BC%9A-240-255.$$$35108512.jpg');)
533-545$$$36543525.jpg');)
%201-13.$$$36600053.jpg');)
;)
Quality Control & SDS
- View current batch:
- Purity: >99.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Shikimic acid is a tri-hydroxy cyclohexene carboxylic acid implicated in biosynthesis of many compounds. The shikimate pathway is named after it. Shikimic acid can be used for the biosynthesis of the aromatic amino acids[1].
Shikimic acid can be isolated from the needles of a variety of plants and microorganisms, such as the Chinese star anise and the seeds of the sweetgum fruit. Shikimic acid can be used as a starting material for the synthesis of oseltamivir. Although shikimic acid is a biosynthetic intermediate existed in most autotrophic organisms general found in very low concentrations [1].
In vitro: In SH-SY5Y cells, 10nM, 10μM, and 10 mM shikimic acid showed antioxidant activity without exerting cytotoxic effects. In addition, shikimic acid protected the cells against H2O2-induced increases in ROS levels and DNA damage. Shikimic acidexhibited neuroprotective actions against oxidative stress-induced toxicity on SH-SY5Y cells [2].
References:
[1].Liza B. Enrich, Margaret L. Scheuermann, Ashley Mohadjer,et al. Liquidambar styraciua: a renewable source of shikimic acid., Tetrahedron Letters, 2008, 49: 2503–2505,
[2].Rabelo T K, Zeidán-Chuliá F, Caregnato F F, et al. In vitro neuroprotective effect of shikimic acid against hydrogen peroxide-induced oxidative stress[J]. Journal of Molecular Neuroscience, 2015, 56(4): 956-965.
| Cas No. | 138-59-0 | SDF | |
| 别名 | 莽草酸 | ||
| 化学名 | (3R,4S,5R)-3,4,5-trihydroxycyclohexene-1-carboxylic acid | ||
| Canonical SMILES | C1C(C(C(C=C1C(=O)O)O)O)O | ||
| 分子式 | C7H10O5 | 分子量 | 174.15 |
| 溶解度 | ≥ 17.4mg/mL in DMSO | 储存条件 | Store at -20°C |
| General tips | 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。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
||
| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
 |
1 mg | 5 mg | 10 mg |
| 1 mM | 5.7422 mL | 28.7109 mL | 57.4218 mL |
| 5 mM | 1.1484 mL | 5.7422 mL | 11.4844 mL |
| 10 mM | 0.5742 mL | 2.8711 mL | 5.7422 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。