Abstract
The solid phase synthesis of a heptapeptideamide with the natural sequence 5-11 of eledoisin is described. The peptide chain is built up stepwise by coupling methionine resin with tert.-butyloxy- carbonyl-amino acids. The cleavage from the resin is achieved in DMF/NH 3. After purification the activity of the peptide is equivalent to a material which was synthesized by classical methods.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.