L-Cysteinesulfinic acid monohydrate
CAS No. 207121-48-0
L-Cysteinesulfinic acid monohydrate ( —— )
产品货号. M28360 CAS No. 207121-48-0
L-Cysteinesulfinic Acid monosculpture 是大鼠代谢型谷氨酸受体 (mGluRs) 的有效激动剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥117 | 有现货 |
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| 5MG | ¥176 | 有现货 |
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| 10MG | ¥282 | 有现货 |
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| 25MG | ¥483 | 有现货 |
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| 50MG | ¥797 | 有现货 |
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| 100MG | ¥1197 | 有现货 |
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| 200MG | ¥1791 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称L-Cysteinesulfinic acid monohydrate
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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
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产品简述L-Cysteinesulfinic Acid monosculpture 是大鼠代谢型谷氨酸受体 (mGluRs) 的有效激动剂。
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产品描述L-Cysteinesulfinic acid monohydrate is a potent agonist at 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.(In Vitro):L-Cysteinesulfinic acid (monohydrate) is an endogenous agonist of a metabotropic receptor coupled to stimulation of phospholipase D (PLD) activity. L-CSA (monohydrate) is an endogenous agonist of the PLD-coupled metabotropic excitatory amino acids (EAA) receptor. L-CSA (monohydrate) selectively activates the PLD-coupled receptor. 1 mM L-CSA (monohydrate) 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 (monohydrate) 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 (monohydrate) is not significantly decreased in the presence of 1 uM tetrodotoxin, suggesting that this response is not dependent upon L-CSA (monohydrate)-induced increases in cell firing.
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体外实验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.
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体内实验——
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同义词——
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通路Neuroscience
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靶点GluR
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number207121-48-0
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分子量171.17
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分子式C3H9NO5S
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : 41.67 mg/mL (243.44 mM)
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SMILESO.N[C@@H](CS(O)=O)C(O)=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Fernandes TS, et al. Phytochemical analysis of bark from Helietta apiculata Benth and antimicrobial activities. Phytochemistry. 2017 Sep;141:131-139.
产品手册
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