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Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery

Open-access drug discovery provides a substantial resource for diseases primarily affecting the poor and disadvantaged. The open-access Pathogen Box collection is comprised of compounds with demonstrated biological activity against specific pathogenic organisms. The supply of this resource by the Me...

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Autores principales: Duffy, Sandra, Sykes, Melissa L., Jones, Amy J., Shelper, Todd B., Simpson, Moana, Lang, Rebecca, Poulsen, Sally-Ann, Sleebs, Brad E., Avery, Vicky M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571359/
https://www.ncbi.nlm.nih.gov/pubmed/28674055
http://dx.doi.org/10.1128/AAC.00379-17
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author Duffy, Sandra
Sykes, Melissa L.
Jones, Amy J.
Shelper, Todd B.
Simpson, Moana
Lang, Rebecca
Poulsen, Sally-Ann
Sleebs, Brad E.
Avery, Vicky M.
author_facet Duffy, Sandra
Sykes, Melissa L.
Jones, Amy J.
Shelper, Todd B.
Simpson, Moana
Lang, Rebecca
Poulsen, Sally-Ann
Sleebs, Brad E.
Avery, Vicky M.
author_sort Duffy, Sandra
collection PubMed
description Open-access drug discovery provides a substantial resource for diseases primarily affecting the poor and disadvantaged. The open-access Pathogen Box collection is comprised of compounds with demonstrated biological activity against specific pathogenic organisms. The supply of this resource by the Medicines for Malaria Venture has the potential to provide new chemical starting points for a number of tropical and neglected diseases, through repurposing of these compounds for use in drug discovery campaigns for these additional pathogens. We tested the Pathogen Box against kinetoplastid parasites and malaria life cycle stages in vitro. Consequently, chemical starting points for malaria, human African trypanosomiasis, Chagas disease, and leishmaniasis drug discovery efforts have been identified. Inclusive of this in vitro biological evaluation, outcomes from extensive literature reviews and database searches are provided. This information encompasses commercial availability, literature reference citations, other aliases and ChEMBL number with associated biological activity, where available. The release of this new data for the Pathogen Box collection into the public domain will aid the open-source model of drug discovery. Importantly, this will provide novel chemical starting points for drug discovery and target identification in tropical disease research.
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spelling pubmed-55713592017-09-05 Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery Duffy, Sandra Sykes, Melissa L. Jones, Amy J. Shelper, Todd B. Simpson, Moana Lang, Rebecca Poulsen, Sally-Ann Sleebs, Brad E. Avery, Vicky M. Antimicrob Agents Chemother Susceptibility Open-access drug discovery provides a substantial resource for diseases primarily affecting the poor and disadvantaged. The open-access Pathogen Box collection is comprised of compounds with demonstrated biological activity against specific pathogenic organisms. The supply of this resource by the Medicines for Malaria Venture has the potential to provide new chemical starting points for a number of tropical and neglected diseases, through repurposing of these compounds for use in drug discovery campaigns for these additional pathogens. We tested the Pathogen Box against kinetoplastid parasites and malaria life cycle stages in vitro. Consequently, chemical starting points for malaria, human African trypanosomiasis, Chagas disease, and leishmaniasis drug discovery efforts have been identified. Inclusive of this in vitro biological evaluation, outcomes from extensive literature reviews and database searches are provided. This information encompasses commercial availability, literature reference citations, other aliases and ChEMBL number with associated biological activity, where available. The release of this new data for the Pathogen Box collection into the public domain will aid the open-source model of drug discovery. Importantly, this will provide novel chemical starting points for drug discovery and target identification in tropical disease research. American Society for Microbiology 2017-08-24 /pmc/articles/PMC5571359/ /pubmed/28674055 http://dx.doi.org/10.1128/AAC.00379-17 Text en Copyright © 2017 Duffy et al. https://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 (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Susceptibility
Duffy, Sandra
Sykes, Melissa L.
Jones, Amy J.
Shelper, Todd B.
Simpson, Moana
Lang, Rebecca
Poulsen, Sally-Ann
Sleebs, Brad E.
Avery, Vicky M.
Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title_full Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title_fullStr Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title_full_unstemmed Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title_short Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery
title_sort screening the medicines for malaria venture pathogen box across multiple pathogens reclassifies starting points for open-source drug discovery
topic Susceptibility
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571359/
https://www.ncbi.nlm.nih.gov/pubmed/28674055
http://dx.doi.org/10.1128/AAC.00379-17
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