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Expanding the Structural Diversity of DNA Methyltransferase Inhibitors

Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show...

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Autores principales: Juárez-Mercado, K. Eurídice, Prieto-Martínez, Fernando D., Sánchez-Cruz, Norberto, Peña-Castillo, Andrea, Prada-Gracia, Diego, Medina-Franco, José L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824300/
https://www.ncbi.nlm.nih.gov/pubmed/33375520
http://dx.doi.org/10.3390/ph14010017
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author Juárez-Mercado, K. Eurídice
Prieto-Martínez, Fernando D.
Sánchez-Cruz, Norberto
Peña-Castillo, Andrea
Prada-Gracia, Diego
Medina-Franco, José L.
author_facet Juárez-Mercado, K. Eurídice
Prieto-Martínez, Fernando D.
Sánchez-Cruz, Norberto
Peña-Castillo, Andrea
Prada-Gracia, Diego
Medina-Franco, José L.
author_sort Juárez-Mercado, K. Eurídice
collection PubMed
description Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show activity with DNMT3B. It was concluded that the dietary component theaflavin is an inhibitor of DNMT1. Two additional novel inhibitors of DNMT1 are the approved drugs glyburide and panobinostat. The DNMT1 enzymatic inhibitory activity of panobinostat, a known pan inhibitor of histone deacetylases, agrees with experimental reports of its ability to reduce DNMT1 activity in liver cancer cell lines. Molecular docking of the active compounds with DNMT1, and re-scoring with the recently developed extended connectivity interaction features approach, led to an excellent agreement between the experimental IC(50) values and docking scores.
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spelling pubmed-78243002021-01-24 Expanding the Structural Diversity of DNA Methyltransferase Inhibitors Juárez-Mercado, K. Eurídice Prieto-Martínez, Fernando D. Sánchez-Cruz, Norberto Peña-Castillo, Andrea Prada-Gracia, Diego Medina-Franco, José L. Pharmaceuticals (Basel) Article Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show activity with DNMT3B. It was concluded that the dietary component theaflavin is an inhibitor of DNMT1. Two additional novel inhibitors of DNMT1 are the approved drugs glyburide and panobinostat. The DNMT1 enzymatic inhibitory activity of panobinostat, a known pan inhibitor of histone deacetylases, agrees with experimental reports of its ability to reduce DNMT1 activity in liver cancer cell lines. Molecular docking of the active compounds with DNMT1, and re-scoring with the recently developed extended connectivity interaction features approach, led to an excellent agreement between the experimental IC(50) values and docking scores. MDPI 2020-12-27 /pmc/articles/PMC7824300/ /pubmed/33375520 http://dx.doi.org/10.3390/ph14010017 Text en © 2020 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
Juárez-Mercado, K. Eurídice
Prieto-Martínez, Fernando D.
Sánchez-Cruz, Norberto
Peña-Castillo, Andrea
Prada-Gracia, Diego
Medina-Franco, José L.
Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title_full Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title_fullStr Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title_full_unstemmed Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title_short Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
title_sort expanding the structural diversity of dna methyltransferase inhibitors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824300/
https://www.ncbi.nlm.nih.gov/pubmed/33375520
http://dx.doi.org/10.3390/ph14010017
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