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Application of Fragment-Based Drug Discovery to Versatile Targets
Fragment-based drug discovery (FBDD) is a powerful method to develop potent small-molecule compounds starting from fragments binding weakly to targets. As FBDD exhibits several advantages over high-throughput screening campaigns, it becomes an attractive strategy in target-based drug discovery. Many...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419598/ https://www.ncbi.nlm.nih.gov/pubmed/32850968 http://dx.doi.org/10.3389/fmolb.2020.00180 |
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author | Li, Qingxin |
author_facet | Li, Qingxin |
author_sort | Li, Qingxin |
collection | PubMed |
description | Fragment-based drug discovery (FBDD) is a powerful method to develop potent small-molecule compounds starting from fragments binding weakly to targets. As FBDD exhibits several advantages over high-throughput screening campaigns, it becomes an attractive strategy in target-based drug discovery. Many potent compounds/inhibitors of diverse targets have been developed using this approach. Methods used in fragment screening and understanding fragment-binding modes are critical in FBDD. This review elucidates fragment libraries, methods utilized in fragment identification/confirmation, strategies applied in growing the identified fragments into drug-like lead compounds, and applications of FBDD to different targets. As FBDD can be readily carried out through different biophysical and computer-based methods, it will play more important roles in drug discovery. |
format | Online Article Text |
id | pubmed-7419598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74195982020-08-25 Application of Fragment-Based Drug Discovery to Versatile Targets Li, Qingxin Front Mol Biosci Molecular Biosciences Fragment-based drug discovery (FBDD) is a powerful method to develop potent small-molecule compounds starting from fragments binding weakly to targets. As FBDD exhibits several advantages over high-throughput screening campaigns, it becomes an attractive strategy in target-based drug discovery. Many potent compounds/inhibitors of diverse targets have been developed using this approach. Methods used in fragment screening and understanding fragment-binding modes are critical in FBDD. This review elucidates fragment libraries, methods utilized in fragment identification/confirmation, strategies applied in growing the identified fragments into drug-like lead compounds, and applications of FBDD to different targets. As FBDD can be readily carried out through different biophysical and computer-based methods, it will play more important roles in drug discovery. Frontiers Media S.A. 2020-08-05 /pmc/articles/PMC7419598/ /pubmed/32850968 http://dx.doi.org/10.3389/fmolb.2020.00180 Text en Copyright © 2020 Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Li, Qingxin Application of Fragment-Based Drug Discovery to Versatile Targets |
title | Application of Fragment-Based Drug Discovery to Versatile Targets |
title_full | Application of Fragment-Based Drug Discovery to Versatile Targets |
title_fullStr | Application of Fragment-Based Drug Discovery to Versatile Targets |
title_full_unstemmed | Application of Fragment-Based Drug Discovery to Versatile Targets |
title_short | Application of Fragment-Based Drug Discovery to Versatile Targets |
title_sort | application of fragment-based drug discovery to versatile targets |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419598/ https://www.ncbi.nlm.nih.gov/pubmed/32850968 http://dx.doi.org/10.3389/fmolb.2020.00180 |
work_keys_str_mv | AT liqingxin applicationoffragmentbaseddrugdiscoverytoversatiletargets |