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Expanding the Structural Diversity of DNA Methyltransferase Inhibitors. | LitMetric

Expanding the Structural Diversity of DNA Methyltransferase Inhibitors.

Pharmaceuticals (Basel)

DIFACQUIM Research Group, Department of Pharmacy, School of Chemistry, National Autonomous University of Mexico, Avenida Universidad 3000, Mexico City 04510, Mexico.

Published: December 2020

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 values and docking scores.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824300PMC
http://dx.doi.org/10.3390/ph14010017DOI Listing

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