Journal article
Overcoming chloroquine resistance in malaria: Design, synthesis and structure-activity relationships of novel chemoreversal agents.
- Abstract:
- Malaria remains a significant infectious disease with even artemisinin-based therapies now facing resistance in the field. Development of new therapies is urgently needed, either by finding new compounds with unique modes of action, or by reversing resistance towards known drugs with 'chemosensitizers' or 'chemoreversal' agents (CRA). Concerning the latter, we have focused on the resistance mechanisms developed against chloroquine (CQ). We have synthesized a series of compounds related to previously identified CRAs, and found promising novel compounds. These compounds show encouraging results in a coumarin labeled chloroquine uptake assay, exhibiting a dose response in resensitising parasites to the antimalarial effects of chloroquine. Selected compounds show consistent potency across a panel of chloroquine and artemisinin sensitive and resistant parasites, and a wide therapeutic window. This data supports further study of CRAs in the treatment of malaria and, ultimately, their use in chloroquine-based combination therapies.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 2.1MB, Terms of use)
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- Publisher copy:
- 10.1016/j.ejmech.2016.04.058
Authors
+ Faculty of Science, National University of Singapore
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- Grant:
- R-148-000-169-133
- Publisher:
- Elsevier
- Journal:
- European Journal of Medicinal Chemistry More from this journal
- Volume:
- 119
- Pages:
- 231-249
- Publication date:
- 2016-04-29
- Acceptance date:
- 2016-04-22
- DOI:
- EISSN:
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1768-3254
- ISSN:
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0223-5234
- Language:
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English
- Keywords:
- Pubs id:
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pubs:623544
- UUID:
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uuid:29c4a487-0a78-4157-8334-030cd297c60b
- Local pid:
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pubs:623544
- Source identifiers:
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623544
- Deposit date:
-
2016-06-08
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier
- Copyright date:
- 2016
- Notes:
- © 2016 Published by Elsevier Masson SAS. This is the accepted manuscript version of the article. The final version is available online from Elsevier at: [10.1016/j.ejmech.2016.04.058]
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