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Diversity and Chemical Space Characterization of Inhibitors of the Epigenetic Target G9a: A Chemoinformatics Approach
[Image: see text] G9a is a histone-lysine methyltransferase that performs the mono- and dimethylation of lysine 9 at histone 3 of the nucleosome. It belongs to the SET PKMT family, and its methylations are related to promoter repression and activation. G9a is a promising epigenetic target. Despite t...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448660/ https://www.ncbi.nlm.nih.gov/pubmed/37636945 http://dx.doi.org/10.1021/acsomega.3c04566 |
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author | Cedillo-González, Raziel Medina-Franco, José L. |
author_facet | Cedillo-González, Raziel Medina-Franco, José L. |
author_sort | Cedillo-González, Raziel |
collection | PubMed |
description | [Image: see text] G9a is a histone-lysine methyltransferase that performs the mono- and dimethylation of lysine 9 at histone 3 of the nucleosome. It belongs to the SET PKMT family, and its methylations are related to promoter repression and activation. G9a is a promising epigenetic target. Despite the fact that there are several G9a inhibitors under development, there are no compounds in clinical use due to adverse in vivo ADMET (absorption, distribution, metabolism, excretion, and toxicity) issues. The goal of this study is to discuss the exploration, characterization, and analysis of the chemical space of 409 G9a inhibitors reported in a large public database. Exploring the chemical space of the inhibitors led to the quantification of their structural diversity based on molecular scaffolds and structural fingerprints of different designs. As part of the analysis, the G9a inhibitors were compared with commercial libraries focused on epigenetic targets. The findings of this work will help in the development of, in a follow-up study, predictive models to identify G9a inhibitors. This study also points out the relevance of screening commercial libraries to expand the epigenetic relevant chemical space, in particular, G9a inhibitors. |
format | Online Article Text |
id | pubmed-10448660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104486602023-08-25 Diversity and Chemical Space Characterization of Inhibitors of the Epigenetic Target G9a: A Chemoinformatics Approach Cedillo-González, Raziel Medina-Franco, José L. ACS Omega [Image: see text] G9a is a histone-lysine methyltransferase that performs the mono- and dimethylation of lysine 9 at histone 3 of the nucleosome. It belongs to the SET PKMT family, and its methylations are related to promoter repression and activation. G9a is a promising epigenetic target. Despite the fact that there are several G9a inhibitors under development, there are no compounds in clinical use due to adverse in vivo ADMET (absorption, distribution, metabolism, excretion, and toxicity) issues. The goal of this study is to discuss the exploration, characterization, and analysis of the chemical space of 409 G9a inhibitors reported in a large public database. Exploring the chemical space of the inhibitors led to the quantification of their structural diversity based on molecular scaffolds and structural fingerprints of different designs. As part of the analysis, the G9a inhibitors were compared with commercial libraries focused on epigenetic targets. The findings of this work will help in the development of, in a follow-up study, predictive models to identify G9a inhibitors. This study also points out the relevance of screening commercial libraries to expand the epigenetic relevant chemical space, in particular, G9a inhibitors. American Chemical Society 2023-08-11 /pmc/articles/PMC10448660/ /pubmed/37636945 http://dx.doi.org/10.1021/acsomega.3c04566 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Cedillo-González, Raziel Medina-Franco, José L. Diversity and Chemical Space Characterization of Inhibitors of the Epigenetic Target G9a: A Chemoinformatics Approach |
title | Diversity and Chemical Space Characterization of Inhibitors
of the Epigenetic Target G9a: A Chemoinformatics Approach |
title_full | Diversity and Chemical Space Characterization of Inhibitors
of the Epigenetic Target G9a: A Chemoinformatics Approach |
title_fullStr | Diversity and Chemical Space Characterization of Inhibitors
of the Epigenetic Target G9a: A Chemoinformatics Approach |
title_full_unstemmed | Diversity and Chemical Space Characterization of Inhibitors
of the Epigenetic Target G9a: A Chemoinformatics Approach |
title_short | Diversity and Chemical Space Characterization of Inhibitors
of the Epigenetic Target G9a: A Chemoinformatics Approach |
title_sort | diversity and chemical space characterization of inhibitors
of the epigenetic target g9a: a chemoinformatics approach |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448660/ https://www.ncbi.nlm.nih.gov/pubmed/37636945 http://dx.doi.org/10.1021/acsomega.3c04566 |
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