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Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs

Building on our earlier work of attaching a chemosensitizer (reversal agent) to a known drug pharmacophore, we have now expanded the structure-activity relationship study to include simplified versions of the chemosensitizer. The change from two aromatic rings in this head group to a single ring doe...

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Autores principales: Gunsaru, Bornface, Burgess, Steven J., Morrill, Westin, Kelly, Jane X., Shomloo, Shawheen, Smilkstein, Martin J., Liebman, Katherine, Peyton, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404532/
https://www.ncbi.nlm.nih.gov/pubmed/28193646
http://dx.doi.org/10.1128/AAC.01913-16
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author Gunsaru, Bornface
Burgess, Steven J.
Morrill, Westin
Kelly, Jane X.
Shomloo, Shawheen
Smilkstein, Martin J.
Liebman, Katherine
Peyton, David H.
author_facet Gunsaru, Bornface
Burgess, Steven J.
Morrill, Westin
Kelly, Jane X.
Shomloo, Shawheen
Smilkstein, Martin J.
Liebman, Katherine
Peyton, David H.
author_sort Gunsaru, Bornface
collection PubMed
description Building on our earlier work of attaching a chemosensitizer (reversal agent) to a known drug pharmacophore, we have now expanded the structure-activity relationship study to include simplified versions of the chemosensitizer. The change from two aromatic rings in this head group to a single ring does not appear to detrimentally affect the antimalarial activity of the compounds. Data from in vitro heme binding and β-hematin inhibition assays suggest that the single aromatic RCQ compounds retain activities against Plasmodium falciparum similar to those of CQ, although other mechanisms of action may be relevant to their activities.
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spelling pubmed-54045322017-05-09 Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs Gunsaru, Bornface Burgess, Steven J. Morrill, Westin Kelly, Jane X. Shomloo, Shawheen Smilkstein, Martin J. Liebman, Katherine Peyton, David H. Antimicrob Agents Chemother Experimental Therapeutics Building on our earlier work of attaching a chemosensitizer (reversal agent) to a known drug pharmacophore, we have now expanded the structure-activity relationship study to include simplified versions of the chemosensitizer. The change from two aromatic rings in this head group to a single ring does not appear to detrimentally affect the antimalarial activity of the compounds. Data from in vitro heme binding and β-hematin inhibition assays suggest that the single aromatic RCQ compounds retain activities against Plasmodium falciparum similar to those of CQ, although other mechanisms of action may be relevant to their activities. American Society for Microbiology 2017-04-24 /pmc/articles/PMC5404532/ /pubmed/28193646 http://dx.doi.org/10.1128/AAC.01913-16 Text en Copyright © 2017 Gunsaru et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Experimental Therapeutics
Gunsaru, Bornface
Burgess, Steven J.
Morrill, Westin
Kelly, Jane X.
Shomloo, Shawheen
Smilkstein, Martin J.
Liebman, Katherine
Peyton, David H.
Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title_full Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title_fullStr Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title_full_unstemmed Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title_short Simplified Reversed Chloroquines To Overcome Malaria Resistance to Quinoline-Based Drugs
title_sort simplified reversed chloroquines to overcome malaria resistance to quinoline-based drugs
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404532/
https://www.ncbi.nlm.nih.gov/pubmed/28193646
http://dx.doi.org/10.1128/AAC.01913-16
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