From lead to market: chemical approaches to transform peptides into therapeutics
| dc.contributor.author | Gare, Caitlin L. | en |
| dc.contributor.author | White, Andrew M. | en |
| dc.contributor.author | Malins, Lara R. | en |
| dc.date.accessioned | 2025-05-29T05:27:48Z | |
| dc.date.available | 2025-05-29T05:27:48Z | |
| dc.date.issued | 2025-02-25 | en |
| dc.description.abstract | Peptides are a powerful drug modality with potential to access difficult targets. This recognition underlies their growth in the global pharmaceutical market, with peptides representing ~8% of drugs approved by the FDA over the past decade. Currently, the peptide therapeutic landscape is evolving, with high-throughput display technologies driving the identification of peptide leads with enhanced diversity. Yet, chemical modifications remain essential for improving the ‘drug-like’ properties of peptides and ultimately translating leads to market. In this review, we explore two recent therapeutic candidates (semaglutide, a peptide hormone analogue, and MK-0616, an mRNA display-derived candidate) as case studies that highlight general approaches to improving pharmacokinetics (PK) and potency. We also emphasize the critical link between advances in medicinal chemistry and the optimisation of highly efficacious peptide therapeutics. | en |
| dc.description.sponsorship | We acknowledge the Australian Research Council (ARC) Centre of Excellence for Innovations in Peptide and Protein Science ( CE200100012 ), the ARC Future Fellowship scheme ( FT240100010 to L.R.M.), the Snow Medical Research Foundation (Fellowship Grant No. SMRF2023-158 to L.R.M.), and the Australian Government Research Training Program PhD Scholarship scheme (C.L.G.) for funding. C.L.G., A.M.W., and L.R.M conceived, wrote and edited the review. BioRender ( BioRender.com ) was used in the creation of the figures. | en |
| dc.description.status | Peer-reviewed | en |
| dc.format.extent | 14 | en |
| dc.identifier.issn | 0968-0004 | en |
| dc.identifier.other | ORCID:/0000-0002-9481-1079/work/185764247 | en |
| dc.identifier.other | ORCID:/0009-0002-4916-7314/work/185764432 | en |
| dc.identifier.scopus | 85219050250 | en |
| dc.identifier.uri | http://www.scopus.com/inward/record.url?scp=85219050250&partnerID=8YFLogxK | en |
| dc.identifier.uri | https://hdl.handle.net/1885/733754376 | |
| dc.language.iso | en | en |
| dc.rights | © 2025 Elsevier Ltd | en |
| dc.source | Trends in Biochemical Sciences | en |
| dc.subject | drug development | en |
| dc.subject | hit-to-lead | en |
| dc.subject | medicinal chemistry | en |
| dc.subject | noncanonical amino acid (ncAA) | en |
| dc.subject | oral bioavailability | en |
| dc.subject | peptide | en |
| dc.title | From lead to market: chemical approaches to transform peptides into therapeutics | en |
| dc.type | Journal article | en |
| dspace.entity.type | Publication | en |
| local.bibliographicCitation.lastpage | 480 | en |
| local.bibliographicCitation.startpage | 467 | en |
| local.contributor.affiliation | Gare, Caitlin L.; Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
| local.contributor.affiliation | White, Andrew M.; Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
| local.contributor.affiliation | Malins, Lara R.; Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
| local.identifier.citationvolume | 50 | en |
| local.identifier.doi | 10.1016/j.tibs.2025.01.009 | en |
| local.identifier.pure | 291dbca1-a9a5-4781-9c17-588b344518b8 | en |
| local.identifier.url | https://www.scopus.com/pages/publications/85219050250 | en |
| local.type.status | Published | en |