Synthesis and Bioactivity of a Cyclopolypeptide from Caribbean Marine Sponge.

Synthesis of a natural proline-rich cyclopolypeptide - rolloamide A was carried out by coupling of tri- and tetrapeptide units Boc-Phe-Pro-Val-OMe and Boc-Pro-Leu-Pro-Ile-OMe after proper deprotection at carboxyl and amino terminals using carbodiimide chemistry in alkaline environment followed by cyclization of linear heptapeptide segment in the presence of base. The structure of synthesized peptide was confirmed by spectral techniques including FTIR, H NMR, C NMR, MS analyses. Newly synthesized peptide was subjected to biological screening against pathogenic microbes and earthworms.