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CAS 24583-23-1

:

N-(Aminocarbonyl)-L-cysteine

Description:
N-(Aminocarbonyl)-L-cysteine, also known by its CAS number 24583-23-1, is a derivative of the amino acid cysteine, characterized by the presence of an aminocarbonyl group attached to the cysteine backbone. This compound features a thiol (-SH) group, which is a hallmark of cysteine, contributing to its reactivity and ability to form disulfide bonds. The aminocarbonyl group introduces additional functional properties, making it a potential candidate for various biochemical applications, including peptide synthesis and as a building block in drug development. N-(Aminocarbonyl)-L-cysteine is typically soluble in water due to its polar functional groups, which enhances its bioavailability in biological systems. Its structural characteristics allow it to participate in redox reactions, and it may play a role in cellular processes involving oxidative stress. As with many amino acid derivatives, its stability and reactivity can be influenced by pH and temperature, making it important to consider these factors in experimental settings. Overall, N-(Aminocarbonyl)-L-cysteine is a versatile compound with potential implications in biochemistry and medicinal chemistry.
Formula:C4H8N2O3S
InChI:InChI=1S/C4H8N2O3S/c5-4(9)6-2(1-10)3(7)8/h2,10H,1H2,(H,7,8)(H3,5,6,9)/t2-/m0/s1
InChI key:InChIKey=APFSAMXTZRYBKF-REOHCLBHSA-N
SMILES:[C@@H](NC(N)=O)(C(O)=O)CS
Synonyms:
  • (2R)-2-(Carbamoylamino)-3-sulfanylpropanoic acid
  • (R)-3-Mercapto-2-ureidopropanoic acid
  • <span class="text-smallcaps">L</span>-Cysteine, N-(aminocarbonyl)-
  • <span class="text-smallcaps">L</span>-Cysteine-N-carbamide
  • <span class="text-smallcaps">L</span>-α-Ureido-β-mercaptopropionic acid
  • Cysteine, N-carbamoyl-, <span class="text-smallcaps">L</span>-
  • L-Cysteine, N-(aminocarbonyl)-
  • L-Cysteine-N-carbamide
  • N-(Aminocarbonyl)-<span class="text-smallcaps">L</span>-cysteine
  • N-(Aminocarbonyl)cysteine
  • See more synonyms
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