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Identifying Promiscuous Compounds with Activity against Different Target Classes
Compounds with multitarget activity are of high interest for polypharmacological drug discovery. Such promiscuous compounds might be active against closely related target proteins from the same family or against distantly related or unrelated targets. Compounds with activity against distinct targets...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891533/ https://www.ncbi.nlm.nih.gov/pubmed/31752252 http://dx.doi.org/10.3390/molecules24224185 |
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author | Feldmann, Christian Miljković, Filip Yonchev, Dimitar Bajorath, Jürgen |
author_facet | Feldmann, Christian Miljković, Filip Yonchev, Dimitar Bajorath, Jürgen |
author_sort | Feldmann, Christian |
collection | PubMed |
description | Compounds with multitarget activity are of high interest for polypharmacological drug discovery. Such promiscuous compounds might be active against closely related target proteins from the same family or against distantly related or unrelated targets. Compounds with activity against distinct targets are not only of interest for polypharmacology but also to better understand how small molecules might form specific interactions in different binding site environments. We have aimed to identify compounds with activity against drug targets from different classes. To these ends, a systematic analysis of public biological screening data was carried out. Care was taken to exclude compounds from further consideration that were prone to experimental artifacts and false positive activity readouts. Extensively assayed compounds were identified and found to contain molecules that were consistently inactive in all assays, active against a single target, or promiscuous. The latter included more than 1000 compounds that were active against 10 or more targets from different classes. These multiclass ligands were further analyzed and exemplary compounds were found in X-ray structures of complexes with distinct targets. Our collection of multiclass ligands should be of interest for pharmaceutical applications and further exploration of binding characteristics at the molecular level. Therefore, these highly promiscuous compounds are made publicly available. |
format | Online Article Text |
id | pubmed-6891533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68915332019-12-18 Identifying Promiscuous Compounds with Activity against Different Target Classes Feldmann, Christian Miljković, Filip Yonchev, Dimitar Bajorath, Jürgen Molecules Article Compounds with multitarget activity are of high interest for polypharmacological drug discovery. Such promiscuous compounds might be active against closely related target proteins from the same family or against distantly related or unrelated targets. Compounds with activity against distinct targets are not only of interest for polypharmacology but also to better understand how small molecules might form specific interactions in different binding site environments. We have aimed to identify compounds with activity against drug targets from different classes. To these ends, a systematic analysis of public biological screening data was carried out. Care was taken to exclude compounds from further consideration that were prone to experimental artifacts and false positive activity readouts. Extensively assayed compounds were identified and found to contain molecules that were consistently inactive in all assays, active against a single target, or promiscuous. The latter included more than 1000 compounds that were active against 10 or more targets from different classes. These multiclass ligands were further analyzed and exemplary compounds were found in X-ray structures of complexes with distinct targets. Our collection of multiclass ligands should be of interest for pharmaceutical applications and further exploration of binding characteristics at the molecular level. Therefore, these highly promiscuous compounds are made publicly available. MDPI 2019-11-18 /pmc/articles/PMC6891533/ /pubmed/31752252 http://dx.doi.org/10.3390/molecules24224185 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Feldmann, Christian Miljković, Filip Yonchev, Dimitar Bajorath, Jürgen Identifying Promiscuous Compounds with Activity against Different Target Classes |
title | Identifying Promiscuous Compounds with Activity against Different Target Classes |
title_full | Identifying Promiscuous Compounds with Activity against Different Target Classes |
title_fullStr | Identifying Promiscuous Compounds with Activity against Different Target Classes |
title_full_unstemmed | Identifying Promiscuous Compounds with Activity against Different Target Classes |
title_short | Identifying Promiscuous Compounds with Activity against Different Target Classes |
title_sort | identifying promiscuous compounds with activity against different target classes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891533/ https://www.ncbi.nlm.nih.gov/pubmed/31752252 http://dx.doi.org/10.3390/molecules24224185 |
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