Synthesis, conformation and immunosuppressive activity of a conformationally restricted cyclosporin lactam analog

JD Aebi, D Guillaume, BE Dunlap…

Index: Aebi; Guillaume; Dunlap; Rich Journal of Medicinal Chemistry, 1988 , vol. 31, # 9 p. 1805 - 1815

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Citation Number: 29

Abstract

Results Synthesis of [Lactam3i4] Cs (4). The synthesis of the peptide portion of [lactam3s4] Cs (4) closely followed the strategy employed by Wengerl'" for synthesis of CsA (Figure 2). The tetra-and heptapeptide fragments 6 and 7 were assembled by the stepwise coupling strategy shown by the arrows (Figure 2) and coupled together to give the undecapeptide 5. The 6-membered lactam dipeptide moiety 8 was synthesized separately (vide infra) and ...