跳转至内容
Merck
CN

S5375

莽草酸

≥99%, suitable for ligand binding assays

别名:

(3R,4S,5R)-(-)-3,4,5-三羟基-1-环己烯羧酸

登录 查看组织和合同定价。

选择尺寸


关于此项目

经验公式(希尔记法):
C7H10O5
化学文摘社编号:
分子量:
174.15
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
205-334-2
MDL number:
Beilstein/REAXYS Number:
2210055
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

莽草酸, ≥99%

InChI

1S/C7H10O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1,4-6,8-10H,2H2,(H,11,12)/t4-,5-,6-/m1/s1

InChI key

JXOHGGNKMLTUBP-HSUXUTPPSA-N

SMILES string

O[C@@H]1CC(=C[C@@H](O)[C@H]1O)C(O)=O

assay

≥99%

form

powder

technique(s)

ligand binding assay: suitable

color

white to off-white

mp

185-187 °C (lit.)

Quality Level

正在寻找类似产品? 访问 产品对比指南

Application

莽草酸已被用作定量测定根部顶端部分莽草酸含量的标准品。它还被用作莽草酸激酶测定的底物。

Biochem/physiol Actions

给药后在大鼠模型中观察到莽草酸具有致癌性。它可用作微生物中芳香族氨基酸、生物碱和其他芳香族代谢物的生物合成的前体。现已确知莽草酸可以抑制二磷酸腺苷(ADP)诱导的兔血小板聚集和血液凝固。

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Efficient elimination of nonstoichiometric enzyme inhibitors from HTS hit lists.
Habig M
Journal of Biomolecular Screening, 14(6), 679-689 (2009)
Inhibitory effects of shikimic acid on platelet aggragation and blood coagulation.
Ma Yi
Acta Pharmaceutica Sinica. B, 35, 1-3 (2000)
Amalia M Estévez et al.
Mini reviews in medicinal chemistry, 12(14), 1443-1454 (2012-07-26)
Shikimic acid, a natural compound is a key intermediate in the biosynthesis of amino acids. Consequently, this derivative is widely present in many plants and has interesting biological properties. But besides the pharmacological relevance of shikimic acid itself, it is
Kai Chen et al.
Bioresource technology, 119, 141-147 (2012-06-26)
Shikimic acid (SA) is an important metabolic intermediate with diverse commercial applications. In this work, antisense RNA interference and gene deletion were carried out to inactivate the aroK gene in an SA-producing Escherichia coli strain, DHPYA-T7. In this strain, the
Varun Rawat et al.
Organic & biomolecular chemistry, 10(20), 3988-3990 (2012-04-24)
A new enantioselective synthesis of the anti-influenza agent (-)-oseltamivir free base (7.1% overall yield; 98% ee) and (-)-methyl 3-epi-shikimate (16% overall yield; 98% ee) has been described from readily available raw materials. Sharpless asymmetric epoxidation and diastereoselective Barbier allylation of

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持