Solid-phase total synthesis of cyclosporine analogues

Soo Y. Ko, Roland M. Wenger

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Syntheses of cyclosporine analogues are reported wherein the peptide couplings were achieved in solid phase. The Wang resin was used as the solid support, and the peptide couplings commenced with the residue 11 of the cyclosporine skeleton. The couplings proceeded in a stepwide manner up to the residue MeBmt1, using symmetric anhydrides. The peptides were then cleaved off the resin, and the cyclization was achieved in solution using Castro's reagent. The solid-phase synthesis described herein offers a very efficient method for the rapid synthesis of structurally diverse cyclosporine analogues in small quantities. The biological activities of the synthetic cyclosporine analogues were evaluated in two in vitro assays, including the IL-2 reporter gene assay and the cyclophilin binding assay. The structure-activity relationship is discussed.

Original languageEnglish
Pages (from-to)695-705
Number of pages11
JournalHelvetica Chimica Acta
Volume80
Issue number3
DOIs
StatePublished - 1997

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