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HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity
West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839297/ https://www.ncbi.nlm.nih.gov/pubmed/20336008 http://dx.doi.org/10.3390/molecules15031690 |
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author | Chung, Dong Hoon Jonsson, Colleen B. Maddox, Clinton McKellip, Sara N. Moore, Blake. P. Heil, Marintha White, E. Lucile Ananthan, Subramaniam Li, Qianjun Feng, Shuang Rasmussen, Lynn |
author_facet | Chung, Dong Hoon Jonsson, Colleen B. Maddox, Clinton McKellip, Sara N. Moore, Blake. P. Heil, Marintha White, E. Lucile Ananthan, Subramaniam Li, Qianjun Feng, Shuang Rasmussen, Lynn |
author_sort | Chung, Dong Hoon |
collection | PubMed |
description | West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughput screen to discover small molecule probes that inhibit virus infection of Vero E6 cells. A primary screen of a 13,001 compound library at a 10 μM final concentration was conducted using the 384-well format. Z′ values ranged from 0.54–0.83 with a median of 0.74. Average S/B was 17 and S/N for each plate ranged from 10.8 to 23.9. Twenty-six compounds showed a dose response in the HT screen and were further evaluated in a time of addition assay and in a titer reduction assay. Seven compounds showed potential as small molecule probes directed at WNV. The hit rate from the primary screen was 0.185% (24 compounds out of 13,001 compounds) and from the secondary screens was 0.053% (7 out of 13,001 compounds) respectively. |
format | Online Article Text |
id | pubmed-4839297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-48392972016-04-21 HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity Chung, Dong Hoon Jonsson, Colleen B. Maddox, Clinton McKellip, Sara N. Moore, Blake. P. Heil, Marintha White, E. Lucile Ananthan, Subramaniam Li, Qianjun Feng, Shuang Rasmussen, Lynn Molecules Article West Nile virus (WNV) is a positive sense, single-stranded RNA virus that can cause illness in humans when transmitted via mosquito vectors. Unfortunately, no antivirals or vaccines are currently available, and therefore efficient and safe antivirals are urgently needed. We developed a high throughput screen to discover small molecule probes that inhibit virus infection of Vero E6 cells. A primary screen of a 13,001 compound library at a 10 μM final concentration was conducted using the 384-well format. Z′ values ranged from 0.54–0.83 with a median of 0.74. Average S/B was 17 and S/N for each plate ranged from 10.8 to 23.9. Twenty-six compounds showed a dose response in the HT screen and were further evaluated in a time of addition assay and in a titer reduction assay. Seven compounds showed potential as small molecule probes directed at WNV. The hit rate from the primary screen was 0.185% (24 compounds out of 13,001 compounds) and from the secondary screens was 0.053% (7 out of 13,001 compounds) respectively. Molecular Diversity Preservation International 2010-03-12 /pmc/articles/PMC4839297/ /pubmed/20336008 http://dx.doi.org/10.3390/molecules15031690 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Chung, Dong Hoon Jonsson, Colleen B. Maddox, Clinton McKellip, Sara N. Moore, Blake. P. Heil, Marintha White, E. Lucile Ananthan, Subramaniam Li, Qianjun Feng, Shuang Rasmussen, Lynn HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title | HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title_full | HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title_fullStr | HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title_full_unstemmed | HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title_short | HTS-Driven Discovery of New Chemotypes with West Nile Virus Inhibitory Activity |
title_sort | hts-driven discovery of new chemotypes with west nile virus inhibitory activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839297/ https://www.ncbi.nlm.nih.gov/pubmed/20336008 http://dx.doi.org/10.3390/molecules15031690 |
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