Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis-Reference-Cited by-同舟云学术

Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis

Published:2024 Issue:1 Volume:15 Page:195-203
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Marschall Edward¹²³^ORCID,Cass Rachel W.¹²³^ORCID,Prasad Komal M.¹²³^ORCID,Swarbrick James D.⁴^ORCID,McKay Alasdair I.⁵^ORCID,Payne Jennifer A. E.¹²³^ORCID,Cryle Max J.¹²³^ORCID,Tailhades Julien¹²³^ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia

2. EMBL Australia, Monash University, Clayton, VIC 3800, Australia

3. ARC Centre of Excellence for Innovations in Peptide and Protein Science, Clayton, VIC 3800, Australia

4. Department of Microbiology, Monash University, Clayton, VIC 3800, Australia

5. Department of Chemistry, Monash University, Clayton, VIC 3800, Australia

Abstract

Optimized solid-phase peptide synthesis (SPPS) conditions allow the incorporation of multiple arylglycine residues which is offering a new perspective on the peptide antibiotic ramoplanin.

Funder

National Health and Medical Research Council

Australian Research Council

Australian Government

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D3SC01944F

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