Studies toward the Total Synthesis of Itralamide B and Biological Evaluation of Its Structural Analogs

Abstract

Itralamides A and B were isolated from the lipophilic extract of Lyngbya majuscula collected from the eastern Caribbean. Itralamide B (1) showed cytotoxic activity towards human embryonic kidney cells (HEK293, IC50 = 6 μM). Preliminary studies disapproved the proposed stereochemistry of itralamide. In this paper, we will provide a full account of the total synthesis of four stereoisomers of itralamide B and the results derived from biological tests of these structural congeners.

Keywords

• itralamide B
• cyclodepsipeptide
• total synthesis
• structural analogs
• biological study