Design and synthesis of analogues of RA-VII-an antitumor bicyclic hexapeptide from Rubiae radix.

J Nat Med

Department of Natural Products and Medicinal Chemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.

Published: September 2021

The 14-membered cycloisodityrosine is the core structure of RA-series antitumor bicyclic peptides obtained from Rubia plants (Rubiaceae). In this study, an efficient method for the synthesis of cycloisodityrosines from commercially available L-tyrosine derivatives was developed. Using synthetic cycloisodityrosines and cycloisodityrosines with modified structures, several RA-VII analogues were designed and synthesized to explore structure-activity relationships of the cycloisodityrosine moiety of the RA-series peptides, and newly isolated natural peptides were synthesized to establish their structures.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397687PMC
http://dx.doi.org/10.1007/s11418-021-01542-wDOI Listing

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