Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Justin F, Coughlan"'
Autor:
Mark L. Smythe, Justin F. Coughlan, Jill Y. Turner, Alun Jones, Douglas A. Horton, Andreas Rühmann, Carolyn Jacobs, Sonya M. Kaiser, Gregory T. Bourne
Publikováno v:
Organicbiomolecular chemistry. 6(8)
Cyclic tetrapeptides are a class of natural products that have been shown to have broad ranging biological activities and good pharmacokinetic properties. In order to synthesise these highly strained compounds a ring contraction strategy had previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8512708f36ccc8c0ea640a2334873fa7
https://pubmed.ncbi.nlm.nih.gov/18385845
https://pubmed.ncbi.nlm.nih.gov/18385845
Autor:
Gregory T, Bourne, Jonathon L, Nielson, Justin F, Coughlan, Paul, Darwen, Marc R, Campitelli, Douglas A, Horton, Andreas, Rhümann, Stephen G, Love, Tran T, Tran, Mark L, Smythe
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 298
Cyclic peptides have been reported to bind to multiple, unrelated classes of receptor with high affinity. Owing to the robustness of amide bond chemistry, the ability to explore extensive chemical diversity by incorporation of unnatural and natural a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3d62a577ef4781dfe5488874897e149
https://pubmed.ncbi.nlm.nih.gov/16044546
https://pubmed.ncbi.nlm.nih.gov/16044546
Autor:
Tran Trung Tran, Gregory T. Bourne, Stephen G. Love, Andreas Rhumann, Justin F. Coughlan, Jonathon L. Nielson, Marc R. Campitelli, Paul J. Darwen, Douglas A. Horton, Mark L. Smythe
Publikováno v:
Peptide Synthesis and Applications ISBN: 9781588293176
Cyclic peptides have been reported to bind to multiple, unrelated classes of receptor with high affinity. Owing to the robustness of amide bond chemistry, the ability to explore extensive chemical diversity by incorporation of unnatural and natural a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b131a6d85185a082e0aa709df3be2be8
https://doi.org/10.1385/1-59259-877-3:151
https://doi.org/10.1385/1-59259-877-3:151
