Four cyclic derivatives of des-Arg9[Leu8]bradykinin have been obtained by classical methods of peptide chemistry. They are cyclo-(-X-Arg-Pro-Pro-Gly-Phe-Gly-Pro-Leu-), where X=Lys or none, and cyclo-(Y-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Leu-), where Y= Lys or Orn. Peptide bonds have been formed by the pentafluorophenylester method, and cyclization has been carried out in a diluted dioxane solution with 40% yield. Subsequent cleavage of protecting groups was made by treatment with hydrogen fluoride. The products obtained were purified by droplet counter-current chromatography. These substances liberate histamine from the rat mast cells comparably to bradykinin and fail to produce myotripic and vascular effects.

Download full-text PDF

Source

Publication Analysis

Top Keywords

[cyclic analogs
4
analogs des-arg9-[leu8]bradykinin]
4
des-arg9-[leu8]bradykinin] cyclic
4
cyclic derivatives
4
derivatives des-arg9[leu8]bradykinin
4
des-arg9[leu8]bradykinin classical
4
classical methods
4
methods peptide
4
peptide chemistry
4
chemistry cyclo--x-arg-pro-pro-gly-phe-gly-pro-leu-
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!