CAS 405150-20-1
:S-1,3-thiazol-2-yl-L-cysteine
Description:
S-1,3-thiazol-2-yl-L-cysteine is a chemical compound characterized by its unique structure, which includes a thiazole ring and an amino acid backbone. The thiazole moiety contributes to its potential biological activity, as thiazoles are often found in various pharmaceuticals and bioactive compounds. This compound features a cysteine residue, which is notable for containing a thiol (-SH) group, making it reactive and capable of forming disulfide bonds. The presence of the sulfur atom in both the thiazole and cysteine enhances its reactivity and potential interactions with other biomolecules. S-1,3-thiazol-2-yl-L-cysteine may exhibit antioxidant properties due to the thiol group, and it could play a role in cellular signaling or as a precursor in the synthesis of other biologically relevant molecules. Its specific applications and effects would depend on further research, particularly in the fields of medicinal chemistry and biochemistry, where such compounds are often explored for therapeutic potential.
Formula:C6H8N2O2S2
InChI:InChI=1/C6H8N2O2S2/c7-4(5(9)10)3-12-6-8-1-2-11-6/h1-2,4H,3,7H2,(H,9,10)/t4-/m0/s1
SMILES:c1csc(n1)SC[C@@H](C(=O)O)N
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Found 4 products.
S-(2-Thiazolyl)-L-Cysteine
CAS:Formula:C6H8N2O2S2Color and Shape:White To Off-White SolidMolecular weight:204.26S-2-Thiazolyl-L-cysteine
CAS:Controlled Product<p>Applications S-2-Thiazolyl-L-cysteine is used in the semisynthetic production of unnatural L-α-amino acids by metabolic engineering of the cysteine-biosynthetic pathway.<br>References Maier, T. H. P., et al.: Nat. Biotechnol., 21, 422 (2003);<br></p>Formula:C6H8N2O2S2Color and Shape:NeatMolecular weight:204.27




