7218-05-5

Usage

Uses

Used in Biochemistry and Pharmacology:
Cysteine, N-benzoylis used as a reagent for the modification and functionalization of proteins and peptides. Its ability to form stable complexes with metal ions and its potential antioxidant properties make it a valuable tool in the study of protein structure and function.
Used in Organic Chemistry:
Cysteine, N-benzoylis used as a reagent in organic chemistry for the synthesis of peptides and proteins. Its versatility in forming stable complexes with metal ions and its potential antioxidant properties contribute to its importance in the development of new compounds and therapeutic agents.
Used in Therapeutic Applications:
Cysteine, N-benzoylhas shown potential therapeutic effects in the treatment of various diseases and disorders. Its potential as a therapeutic agent makes it an important target for further research and development in the field of medicine.

Upstream product

• 921-01-7 rac-cysteine 
• 98-88-4 benzoyl chloride 
• 139776-07-1 C₁₄H₁₁NOS 
• 1571113-40-0 C₁₄H₁₀FNOS 
• 1571113-41-1 C₁₅H₁₁NO₃S 
• 145198-44-3 C₁₅H₁₃NO₂S 
• 1571113-44-4 C₁₂H₁₅NOS 
• 1571113-45-5 C₁₅H₁₃NOS 
• 1571113-46-6 C₁₅H₁₂FNOS 
• 1571113-47-7 C₁₆H₁₅NO₂S 
• 2227-79-4 benzenecarbothioamide 
• 116179-35-2 2-Phenyl-2-thiazolin-4-carbonsaeure-hydrochlorid 
• 25129-20-8 N,N'-dibenzoyl-DL-cystine 

Downstream Products

• 52-90-4 L-Cysteine 
• 7217-84-7 2-benzamido-3-mercaptopropanoic acid 
• 64514-88-1 Hg(O₂CCH(NH₂COC₆H₅)CH₂S)2 

Relevant academic research and scientific papers

S-aroylthiooximes: A facile route to hydrogen sulfide releasing compounds with structure-dependent release kinetics

We report the facile preparation of a family of S-aroylthiooxime (SATO) H2S donors, which are synthesized via a click reaction analogous to oxime formation between S-aroylthiohydroxylamines (SATHAs) and aldehydes or ketones. Analysis of cysteine-triggered H2S release revealed structure-dependent release kinetics with half-lives from 8-82 min by substitution of the SATHA ring. The pseudo-first-order rate constants of substituted SATOs fit standard linear free energy relationships (p = 1.05), demonstrating a significant sensitivity to electronic effects.

Beauveria bassiana ATCC 7159 contains an L-specific α-amino acid benzamidase

Biotransformation of a series of racemic N-benzoyl α-amino acids by the fungus Beauveria bassiana ATCC 7159 results in isolation of the corresponding D-amino acid benzamides in high enantiomeric purity and yield.

Amino Acids, 12. - Syntheses of DL-Cysteines from Acrylic Acid Derivatives

The addition of sulfenyl chlorides 1 to 2-alkenoic acid esters 2 gives mixtures of 2(3)-chloro-3(2)-thioalkenoic acid esters 3/4, whereas the addition of thiols 7 to methyl 2-chloro-2-propenoate (6) results in the formation of methyl 2-chloro-3-thiopropanoates 3 only.The dependence of the isomerization of 3 to 4 on the reaction conditions was investigated; at higher temperatures the formation of 4 is especially favored.At temperatures below 55 deg C the 2-azido compounds 8 are obtained without isomerization from 3 by reaction with sodium azide in the presence of a PT catalyst.Cysteine derivatives 9 or 10, resp., are obtained by hydrogenation of 8 with H2S/pyridine/H2O or with H2/Re2S; the overall yields of 9 or 10, resp., starting from 6 are as high as 70percent.DL-Cysteine is obtained in good overall yields as hydrochloride hydrate 16 by HCl-catalyzed hydrolysis of the 2-thiazolines 15a*HCl and 15e, which are prepared by HCl-catalyzed addition of thioacetamide (11a) to α-chloroacrylic acid (12) or the amide 13 and consecutive ring closure.