L-Cysteinesulfinic acid monohydrate (Synonyms: L-半胱亚磺酸)

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L-Cysteinesulfinic acid monohydrate  (Synonyms: L-半胱亚磺酸) 纯度: 99.81%

L-Cysteinesulfinic acid monohydrate 是一种有效的代谢型谷氨酸受体 (mGluRs) 激动剂,作用于 mGluR1,mGluR5,mGluR2,mGluR4,mGluR6 和 mGluR8,pEC50 分别为 3.92,4.6,3.9,2.7,4.0,和 3.94。

L-Cysteinesulfinic acid monohydrate                                          (Synonyms: L-半胱亚磺酸)

L-Cysteinesulfinic acid monohydrate Chemical Structure

CAS No. : 207121-48-0

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生物活性

L-Cysteinesulfinic acid monohydrate is a potent agonist at several rat metabotropic glutamate receptors (mGluRs) with pEC50s of 3.92, 4.6, 3.9, 2.7, 4.0, and 3.94 for mGluR1, mGluR5, mGluR2, mGluR4, mGluR6, and mGluR8, respectively[1].

IC50 & Target[1]

mGluR1

3.92 (pEC50)

mGluR2

3.9 (pEC50)

mGluR4

2.7 (pEC50)

mGluR5

4.6 (pEC50)

mGluR6

4.0 (pEC50)

mGluR8

3.94 (pEC50)

Human Endogenous Metabolite

 

体外研究
(In Vitro)

L-Cysteinesulfinic acid is an endogenous agonist of a metabotropic receptor coupled to stimulation of phospholipase D (PLD) activity. L-CSA is an endogenous agonist of the PLD-coupled metabotropic excitatory amino acids (EAA) receptor. L-CSA selectively activates the PLD-coupled receptor. 1 mM L-CSA induces a significant increase in PLD activity in hippocampal slices, whereas 1 mM concentrations of L-glutamate, L-aspartate, and L-HCA are without effect. L-CSA elicits a dose-dependent increase in PLD activity in rat hippocampal slices in the presence of iGluR antagonists, with an approximate EC50 of 500 uM. The PLD response induced by 1 mM L-CSA is not significantly decreased in the presence of 1 uM tetrodotoxin, suggesting that this response is not dependent upon L-CSA-induced increases in cell firing[1].

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

L-Cysteinesulfinic acid monohydrate 相关抗体:

分子量

171.17

Formula

C3H9NO5S

CAS 号

207121-48-0

性状

固体

颜色

White to off-white

中文名称

L-半胱氨酸亚磺酸一水合物

结构分类
  • Others
初始来源
  • 内源性代谢物
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

H2O 中的溶解度 : 41.67 mg/mL (243.44 mM; 超声助溶)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 5.8421 mL 29.2107 mL 58.4215 mL
5 mM 1.1684 mL 5.8421 mL 11.6843 mL
10 mM 0.5842 mL 2.9211 mL 5.8421 mL

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储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-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。

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

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体积 (start)

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工作液所需浓度 : mg/mL

该产品水溶性佳,请具体参考实测 水 / PBS / Saline 中的溶解度数据。
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纯度 & 产品资料

纯度: 99.81%

Data Sheet (601 KB) SDS (392 KB)

COA (172 KB) LCMS (87 KB)

产品使用指南 (1538 KB)

参考文献
  • [1]. Shi Q, et al. L-homocysteine sulfinic acid and other acidic homocysteine derivatives are potent and selective metabotropic glutamate receptor agonists. J Pharmacol Exp Ther. 2003 Apr;305(1):131-42.  [Content Brief]

    [2]. Boss V, et al. L-cysteine sulfinic acid as an endogenous agonist of a novel metabotropic receptor coupled to stimulation of phospholipase D activity.  [Content Brief]

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