H.L. Bolt
Enlarging the chemical space of anti-leishmanials: a structure-activity relationship study of peptoids against Leishmania mexicana, a causative agent of cutaneous leishmaniasis
Bolt, H.L.; Eggimann, G.A.; Denny, P.W.; Cobb, S.L.
Authors
G.A. Eggimann
Professor Paul Denny p.w.denny@durham.ac.uk
Professor
Professor Steven Cobb s.l.cobb@durham.ac.uk
Professor
Abstract
Peptoids, a class of peptide mimetics, have emerged as promising anti-infective agents against a range of bacterial and fungal infections. Recently we have shown peptoids to be novel anti-parasitic and, specifically, anti-leishmanial, compounds. In this study, we have expanded the chemical space of our peptoid library and have identified peptoids with low micromolar activity against Leishmania mexicana axenic amastigotes and significantly, the first peptoids with promising activity against intracellular amastigotes, which are the clinical cause of cutaneous leishmaniasis.
Citation
Bolt, H., Eggimann, G., Denny, P., & Cobb, S. (2016). Enlarging the chemical space of anti-leishmanials: a structure-activity relationship study of peptoids against Leishmania mexicana, a causative agent of cutaneous leishmaniasis. MedChemComm, 7(5), 799-805. https://doi.org/10.1039/c6md00060f
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 10, 2016 |
Online Publication Date | Mar 15, 2016 |
Publication Date | May 1, 2016 |
Deposit Date | Jan 27, 2016 |
Publicly Available Date | Mar 31, 2016 |
Journal | MedChemComm. |
Print ISSN | 2040-2503 |
Electronic ISSN | 2040-2511 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 7 |
Issue | 5 |
Pages | 799-805 |
DOI | https://doi.org/10.1039/c6md00060f |
Public URL | https://durham-repository.worktribe.com/output/1414237 |
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Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/
Copyright Statement
Advance online version This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
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