
L-Cysteinesulfinic acid monohydrate
CAS No. 207121-48-0
L-Cysteinesulfinic acid monohydrate( —— )
Catalog No. M28360 CAS No. 207121-48-0
L-Cysteinesulfinic acid monohydrate is a potent agonist at rat metabotropic glutamate receptors (mGluRs).
Purity : >98% (HPLC)






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10MG | 35 | Get Quote |
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25MG | 71 | Get Quote |
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50MG | 110 | Get Quote |
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100MG | 160 | Get Quote |
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Biological Information
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Product NameL-Cysteinesulfinic acid monohydrate
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NoteResearch use only, not for human use.
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Brief DescriptionL-Cysteinesulfinic acid monohydrate is a potent agonist at rat metabotropic glutamate receptors (mGluRs).
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DescriptionL-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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In VitroL-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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In Vivo——
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Synonyms——
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PathwayNeuroscience
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TargetGluR
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number207121-48-0
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Formula Weight171.17
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Molecular FormulaC3H9NO5S
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Purity>98% (HPLC)
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SolubilityIn 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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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Fernandes TS, et al. Phytochemical analysis of bark from Helietta apiculata Benth and antimicrobial activities. Phytochemistry. 2017 Sep;141:131-139.
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