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Strategies For Peptide Macrocyclization - Head To Tail Cyclization
Strategies For Peptide Macrocyclization - Head To Tail Cyclization
Strategies For Peptide Macrocyclization - Head To Tail Cyclization
cyclization
https://www.lifetein.com/cyclic-peptide-disulfide-bonds.html
Bioactive head-to-tail cyclic peptides are promising lead structures for the development of new
pharmaceuticals with their high selectivity, potency, and improved enzymatic stability.
Cyclic peptides are usually synthesized with an N-terminal amide linkage that closes the ring
structure with a C-terminal carboxylic acid. The current methods for amide formation are
expensive and inelegant as the top challenge for organic chemistry. The issues of waste and
expense associated with amide formation are responsible for the enormous cost of commercial
therapeutic peptides. The reaction typically renders a very low yield.
Recently, LifeTein developed a single-step preparation of the amide cyclization with a high yield.
The resulting peptide macrocycles are conformationally stable with multiple intramolecular
hydrogen bonds. LifeTein’s advances in amide-forming methodologies can have far-reaching
impacts across scientific disciplines. The unnatural amino acids can be easily incorporated during
the synthesis for stability or enhanced activity, or specific probes for interrogating binding and
biological function during the synthesis. The improved amide-forming chemical reactions will
not damage the structure of any unnatural amino acids.