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Open Source Drug Discovery: Highly Potent Antimalarial Compounds Derived from the Tres Cantos Arylpyrroles
[Image: see text] The development of new antimalarial compounds remains a pivotal part of the strategy for malaria elimination. Recent large-scale phenotypic screens have provided a wealth of potential starting points for hit-to-lead campaigns. One such public set is explored, employing an open sour...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084075/ https://www.ncbi.nlm.nih.gov/pubmed/27800551 http://dx.doi.org/10.1021/acscentsci.6b00086 |
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author | Williamson, Alice E. Ylioja, Paul M. Robertson, Murray N. Antonova-Koch, Yevgeniya Avery, Vicky Baell, Jonathan B. Batchu, Harikrishna Batra, Sanjay Burrows, Jeremy N. Bhattacharyya, Soumya Calderon, Felix Charman, Susan A. Clark, Julie Crespo, Benigno Dean, Matin Debbert, Stefan L. Delves, Michael Dennis, Adelaide S. M. Deroose, Frederik Duffy, Sandra Fletcher, Sabine Giaever, Guri Hallyburton, Irene Gamo, Francisco-Javier Gebbia, Marinella Guy, R. Kiplin Hungerford, Zoe Kirk, Kiaran Lafuente-Monasterio, Maria J. Lee, Anna Meister, Stephan Nislow, Corey Overington, John P. Papadatos, George Patiny, Luc Pham, James Ralph, Stuart A. Ruecker, Andrea Ryan, Eileen Southan, Christopher Srivastava, Kumkum Swain, Chris Tarnowski, Matthew J. Thomson, Patrick Turner, Peter Wallace, Iain M. Wells, Timothy N. C. White, Karen White, Laura Willis, Paul Winzeler, Elizabeth A. Wittlin, Sergio Todd, Matthew H. |
author_facet | Williamson, Alice E. Ylioja, Paul M. Robertson, Murray N. Antonova-Koch, Yevgeniya Avery, Vicky Baell, Jonathan B. Batchu, Harikrishna Batra, Sanjay Burrows, Jeremy N. Bhattacharyya, Soumya Calderon, Felix Charman, Susan A. Clark, Julie Crespo, Benigno Dean, Matin Debbert, Stefan L. Delves, Michael Dennis, Adelaide S. M. Deroose, Frederik Duffy, Sandra Fletcher, Sabine Giaever, Guri Hallyburton, Irene Gamo, Francisco-Javier Gebbia, Marinella Guy, R. Kiplin Hungerford, Zoe Kirk, Kiaran Lafuente-Monasterio, Maria J. Lee, Anna Meister, Stephan Nislow, Corey Overington, John P. Papadatos, George Patiny, Luc Pham, James Ralph, Stuart A. Ruecker, Andrea Ryan, Eileen Southan, Christopher Srivastava, Kumkum Swain, Chris Tarnowski, Matthew J. Thomson, Patrick Turner, Peter Wallace, Iain M. Wells, Timothy N. C. White, Karen White, Laura Willis, Paul Winzeler, Elizabeth A. Wittlin, Sergio Todd, Matthew H. |
author_sort | Williamson, Alice E. |
collection | PubMed |
description | [Image: see text] The development of new antimalarial compounds remains a pivotal part of the strategy for malaria elimination. Recent large-scale phenotypic screens have provided a wealth of potential starting points for hit-to-lead campaigns. One such public set is explored, employing an open source research mechanism in which all data and ideas were shared in real time, anyone was able to participate, and patents were not sought. One chemical subseries was found to exhibit oral activity but contained a labile ester that could not be replaced without loss of activity, and the original hit exhibited remarkable sensitivity to minor structural change. A second subseries displayed high potency, including activity within gametocyte and liver stage assays, but at the cost of low solubility. As an open source research project, unexplored avenues are clearly identified and may be explored further by the community; new findings may be cumulatively added to the present work. |
format | Online Article Text |
id | pubmed-5084075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50840752016-10-31 Open Source Drug Discovery: Highly Potent Antimalarial Compounds Derived from the Tres Cantos Arylpyrroles Williamson, Alice E. Ylioja, Paul M. Robertson, Murray N. Antonova-Koch, Yevgeniya Avery, Vicky Baell, Jonathan B. Batchu, Harikrishna Batra, Sanjay Burrows, Jeremy N. Bhattacharyya, Soumya Calderon, Felix Charman, Susan A. Clark, Julie Crespo, Benigno Dean, Matin Debbert, Stefan L. Delves, Michael Dennis, Adelaide S. M. Deroose, Frederik Duffy, Sandra Fletcher, Sabine Giaever, Guri Hallyburton, Irene Gamo, Francisco-Javier Gebbia, Marinella Guy, R. Kiplin Hungerford, Zoe Kirk, Kiaran Lafuente-Monasterio, Maria J. Lee, Anna Meister, Stephan Nislow, Corey Overington, John P. Papadatos, George Patiny, Luc Pham, James Ralph, Stuart A. Ruecker, Andrea Ryan, Eileen Southan, Christopher Srivastava, Kumkum Swain, Chris Tarnowski, Matthew J. Thomson, Patrick Turner, Peter Wallace, Iain M. Wells, Timothy N. C. White, Karen White, Laura Willis, Paul Winzeler, Elizabeth A. Wittlin, Sergio Todd, Matthew H. ACS Cent Sci [Image: see text] The development of new antimalarial compounds remains a pivotal part of the strategy for malaria elimination. Recent large-scale phenotypic screens have provided a wealth of potential starting points for hit-to-lead campaigns. One such public set is explored, employing an open source research mechanism in which all data and ideas were shared in real time, anyone was able to participate, and patents were not sought. One chemical subseries was found to exhibit oral activity but contained a labile ester that could not be replaced without loss of activity, and the original hit exhibited remarkable sensitivity to minor structural change. A second subseries displayed high potency, including activity within gametocyte and liver stage assays, but at the cost of low solubility. As an open source research project, unexplored avenues are clearly identified and may be explored further by the community; new findings may be cumulatively added to the present work. American Chemical Society 2016-09-14 2016-10-26 /pmc/articles/PMC5084075/ /pubmed/27800551 http://dx.doi.org/10.1021/acscentsci.6b00086 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Williamson, Alice E. Ylioja, Paul M. Robertson, Murray N. Antonova-Koch, Yevgeniya Avery, Vicky Baell, Jonathan B. Batchu, Harikrishna Batra, Sanjay Burrows, Jeremy N. Bhattacharyya, Soumya Calderon, Felix Charman, Susan A. Clark, Julie Crespo, Benigno Dean, Matin Debbert, Stefan L. Delves, Michael Dennis, Adelaide S. M. Deroose, Frederik Duffy, Sandra Fletcher, Sabine Giaever, Guri Hallyburton, Irene Gamo, Francisco-Javier Gebbia, Marinella Guy, R. Kiplin Hungerford, Zoe Kirk, Kiaran Lafuente-Monasterio, Maria J. Lee, Anna Meister, Stephan Nislow, Corey Overington, John P. Papadatos, George Patiny, Luc Pham, James Ralph, Stuart A. Ruecker, Andrea Ryan, Eileen Southan, Christopher Srivastava, Kumkum Swain, Chris Tarnowski, Matthew J. Thomson, Patrick Turner, Peter Wallace, Iain M. Wells, Timothy N. C. White, Karen White, Laura Willis, Paul Winzeler, Elizabeth A. Wittlin, Sergio Todd, Matthew H. Open Source Drug Discovery: Highly Potent Antimalarial Compounds Derived from the Tres Cantos Arylpyrroles |
title | Open Source Drug Discovery: Highly Potent Antimalarial
Compounds Derived from the Tres Cantos Arylpyrroles |
title_full | Open Source Drug Discovery: Highly Potent Antimalarial
Compounds Derived from the Tres Cantos Arylpyrroles |
title_fullStr | Open Source Drug Discovery: Highly Potent Antimalarial
Compounds Derived from the Tres Cantos Arylpyrroles |
title_full_unstemmed | Open Source Drug Discovery: Highly Potent Antimalarial
Compounds Derived from the Tres Cantos Arylpyrroles |
title_short | Open Source Drug Discovery: Highly Potent Antimalarial
Compounds Derived from the Tres Cantos Arylpyrroles |
title_sort | open source drug discovery: highly potent antimalarial
compounds derived from the tres cantos arylpyrroles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084075/ https://www.ncbi.nlm.nih.gov/pubmed/27800551 http://dx.doi.org/10.1021/acscentsci.6b00086 |
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