1361315-34-5

Upstream product

• 1361315-33-4 GABA-L-Cys(S-Cbz-L-Ala)-OH hydrochloride 
• 1361315-32-3 Boc-GABA-Cys(S-Cbz-L-Ala)-OH 
• 1361315-31-2 Boc-GABA-L-Cys-OH 

Downstream Products

• 1361315-35-6 Boc-Gly-GABA-L-Cys(S-Cbz-L-Ala)-OH 
• 1383120-37-3 C₃₁H₃₉N₅O₁₀S 
• 1383120-32-8 C₄₀H₅₄N₈O₁₄S₂ 

Relevant academic research and scientific papers

Long-range intramolecular s → N acyl migration: A study of the formation of native peptide analogues via 13-, 15-, and 16-membered cyclic transition states

The intramolecular long-range S → N acyl migration via 13-, 15-, and 16-membered cyclic transition states to form native tetra- and pentapeptide analogues was studied on S-acylcysteine peptides containing β- or γ-amino acids. The pH-dependency study of the acyl migration via a 15-membered cyclic transition state indicated that the reaction is favored at a pH range from 7.0 to 7.6. Experimental observations are supported by structural and computational investigations.