66127-60-4Relevant academic research and scientific papers
Development of Dipeptidic hGPR54 Agonists
Doebelin, Christelle,Bertin, Isabelle,Schneider, Séverine,Schmitt, Martine,Bourguignon, Jean-Jacques,Ancel, Caroline,Simonneaux, Valerie,Simonin, Frédéric,Bihel, Frédéric
, p. 2147 - 2154 (2016/11/04)
A series of dipeptides were designed as potential agonists of the human KiSS1-derived peptide receptor (hGPR54). While the sequence Arg-Trp-NH2was the most efficient in terms of affinity, we established a convergent synthetic strategy to optimi
Peptide Synthesis Catalyzed by Modified α-Chymotrypsin in Low-Water Organic Media
Gaertner, H.,Watanabe, T.,Sinisterra, J. V.,Puigserver, A.
, p. 3149 - 3153 (2007/10/02)
Enzyme-catalyzed synthesis of peptide bonds in organic solvents has been investigated by using α-chymotrypsin either modified with poly(ethylene glycol) or immobilized on different supports, in order to find out the importance of water content in the reaction.High yields of peptide synthesis were obtained whatever the type of enzyme derivative used.By varying the type of support, a modification in the enzyme environment was observed and resulted in a significant increase in the reaction yield when nucleophiles with poor affinity for the enzyme were used.Since organic solvents also affected substrate specificity with respect to the donor ester, a general methodology was proposed for the enzymatic synthesis of peptides in low-water organic media.
