Cargando…

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

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 cycl...

Descripción completa

Detalles Bibliográficos
Autor principal: Hitotsuyanagi, Yukio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397687/
https://www.ncbi.nlm.nih.gov/pubmed/34244894
http://dx.doi.org/10.1007/s11418-021-01542-w
_version_ 1783744669982654464
author Hitotsuyanagi, Yukio
author_facet Hitotsuyanagi, Yukio
author_sort Hitotsuyanagi, Yukio
collection PubMed
description 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. GRAPHIC ABSTRACT: [Image: see text]
format Online
Article
Text
id pubmed-8397687
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Singapore
record_format MEDLINE/PubMed
spelling pubmed-83976872021-09-15 Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix Hitotsuyanagi, Yukio J Nat Med Review 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. GRAPHIC ABSTRACT: [Image: see text] Springer Singapore 2021-07-10 2021 /pmc/articles/PMC8397687/ /pubmed/34244894 http://dx.doi.org/10.1007/s11418-021-01542-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Hitotsuyanagi, Yukio
Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title_full Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title_fullStr Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title_full_unstemmed Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title_short Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix
title_sort design and synthesis of analogues of ra-vii—an antitumor bicyclic hexapeptide from rubiae radix
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397687/
https://www.ncbi.nlm.nih.gov/pubmed/34244894
http://dx.doi.org/10.1007/s11418-021-01542-w
work_keys_str_mv AT hitotsuyanagiyukio designandsynthesisofanaloguesofraviianantitumorbicyclichexapeptidefromrubiaeradix