L-Cysteine S-sulfate sodium hydrate

Modify Date: 2025-08-25 10:19:12

L-Cysteine S-sulfate sodium hydrate structure	Common Name	L-Cysteine S-sulfate sodium hydrate
	CAS Number	150465-29-5	Molecular Weight	500.45
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₆H₁₈N₂Na₂O₁₃S₄	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of L-Cysteine S-sulfate sodium hydrate

L-Cysteine S-sulfate sodium hydrate is a potent N-methyl-d-aspartate (NMDA) glutamatergic receptors agonist. L-Cysteine S-sulfate sodium hydrate is the substrate for cystine lyase, it can be used in mass spectrometry operations[1][2].

Name	L-Cysteine S-sulfate sodium salt sesquihydrate
Synonym	More Synonyms

Description	L-Cysteine S-sulfate sodium hydrate is a potent N-methyl-d-aspartate (NMDA) glutamatergic receptors agonist. L-Cysteine S-sulfate sodium hydrate is the substrate for cystine lyase, it can be used in mass spectrometry operations[1][2].
Related Catalog	Signaling Pathways >> Neuronal Signaling >> iGluR Research Areas >> Neurological Disease Signaling Pathways >> Membrane Transporter/Ion Channel >> iGluR
References	[1]. Steventon GB, et, al. Comparison of the sulfur-oxygenation of cysteine and S-carboxymethyl-l-cysteine in human hepatic cytosol and the rôle of cysteine dioxygenase. J Pharm Pharmacol. 2018 Aug;70(8):1069-1077. [2]. Macaluso V, et al. l-Cysteine Modified by S-Sulfation: Consequence on Fragmentation Processes Elucidated by Tandem Mass Spectrometry and Chemical Dynamics Simulations. J Phys Chem A. 2019 May 2;123(17):3685-3696.

Description

Related Catalog

Signaling Pathways >> Neuronal Signaling >> iGluR

Research Areas >> Neurological Disease

Signaling Pathways >> Membrane Transporter/Ion Channel >> iGluR

References

[1]. Steventon GB, et, al. Comparison of the sulfur-oxygenation of cysteine and S-carboxymethyl-l-cysteine in human hepatic cytosol and the rôle of cysteine dioxygenase. J Pharm Pharmacol. 2018 Aug;70(8):1069-1077.

[2]. Macaluso V, et al. l-Cysteine Modified by S-Sulfation: Consequence on Fragmentation Processes Elucidated by Tandem Mass Spectrometry and Chemical Dynamics Simulations. J Phys Chem A. 2019 May 2;123(17):3685-3696.