1637-71-4
1637-71-4
Chemical Structure
L-Cysteine S-sulfate
- CAS No.: 1637-71-4
- Formula:C3H7NO5S2
- Molecular Weight:201.22
IUPAC Name: S-sulfo-L-cysteine
InChIKey: NOKPBJYHPHHWAN-REOHCLBHSA-N
SMILES: N[C@@H](CSS(=O)(O)=O)C(O)=O
Biological Activity: L-Cysteine S-sulfate is an S-sulfated derivative of L-cysteine (HY-Y0337). L-Cysteine S-sulfate is the substrate for cystine lyase, it can be used in mass spectrometry and chromatography analyses[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
L-Cysteine S-sulfate | 99.65% | L-Cysteine S-sulfate is an S-sulfated derivative of L-cysteine (HY-Y0337). L-Cysteine S-sulfate is the substrate for cystine lyase, it can be used in mass spectrometry and chromatography analyses. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
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. [Content Brief]
- [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. [Content Brief]
Keywords
