Figure 1.
Structures of alamethicin F50 (1), ortho-F-Pheol alamethicin F50 (2), meta-F-Pheol alamethicin F50 (3), trichokonin VI (4), ortho-F-Pheol trichokonin VI (5), and meta-F-Pheol trichokonin VI (6). The amino acid residue targeted for modification is highlighted in blue, whereas the red residues highlight the difference between alamethicin F50 (1) and trichokonin VI (4).