2018年12月24日星期一

A Perfluoroaryl-Cysteine SNAr Chemistry Approach to Unprotected Peptide Stapling

A Perfluoroaryl-Cysteine SNAr Chemistry Approach to Unprotected Peptide Stapling

AM Spokoyny, Y Zou, JJ Ling, H Yu… - Journal of the …, 2013 - ACS Publications
We report the discovery of a facile transformation between perfluoroaromatic molecules and
a cysteine thiolate, which is arylated at room temperature. This new approach enabled us to
selectively modify cysteine residues in unprotected peptides, providing access to variants …


For custom peptides, please visit www.pepmic.com. Our peptide services including but not limited to:
*Peptide Synthesis: From short peptides to long peptides, linear peptides to cyclic peptides.
*Peptide Modifications: Peptide-protein conjugation, D-amino acid peptides, isotope peptides, fluorescent peptides, multiple antigen peptides, multiple disulfide bridge peptides, phosphopeptides etc.
*Catalog Peptides: ACE Inhibitors, Amyloids & Related Peptides, Antimicrobial Peptides, Apelin Peptides, Myelin Oligodendrocyte Glycoprotein (MOG) Peptides, TAT Proteins etc.
*Peptide Salt: TFA, Desalt, Acetate, HCl.
*Peptide Purity: From crude to >99.5%.
*Production Capacity: From mg to kg, with a capacity of synthesizing 15,000 peptides/month.
*Peptide Library Synthesis: Alanine Scan, Overlapping, Positional Scan, T-cell Truncated, Scrambled ect.

Eva He
eva@pepmic.com
Pepmic Co., Ltd
www.pepmic.com


没有评论:

发表评论