| 摘要 |
Cyclic pentapeptides are disclosed having the following formula (I)-Cyclo(-A1-A2-A3-A4-A5-)-wherein A1, A2, A3, A4 and A5 are amino acid residues. The pentapeptide has amino acid residues in positions 1-2-3 to form a gamma-turn, and amino acid residues in positions 3-4-5-1 to form a beta-turn in combination with the gamma-turn. D-alpha-amino acid residues are selected for A1, A3, and A5 and L-alpha-amino acid residues are selected for A2 and A4. Compounds having gamma-turns and beta-turns can be synthesized, regardless of the kinds of amino acid residues, and it is possible to synthesize compounds in which desired amino acid residues are introduced into sites of beta-turn and gamma-turn based on their importance from the viewpoint of biological activity. The present invention is therefore available for design of compounds having biological activity.
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