Synthesis, and Structural and Biological Studies of Efrapeptin C Analogues

Abstract

Abstract A series of analogues of efrapeptin C ( 1 ), with variations in the central tripeptide epitope (positions 6–8), were prepared by a combination of solid‐ and solution‐phase peptide syntheses. The conformations of the modified compounds 2 – 6 were investigated by circular‐dichroism (CD) spectroscopy to differentiate between 3 10 ‐ and α ‐helical secondary structures. The inhibitory activities of the new compounds towards F 1 ‐ATPase from E. coli were determined. The modified congeners 3 – 5 were less active by one order of magnitude compared to 1 ( K i 10 μ M ), and 6 was completely inactive. Our experiments demonstrate that the flexible, central tripeptide epitope, comprising positions 6–8 in 1 , is crucial for molecular recognition, even slight sequence modifications being hardly tolerated.