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拓展DNA甲基转移酶抑制剂的结构多样性

Expanding the Structural Diversity of DNA Methyltransferase Inhibitors.

作者信息

Juárez-Mercado K Eurídice, Prieto-Martínez Fernando D, Sánchez-Cruz Norberto, Peña-Castillo Andrea, Prada-Gracia Diego, Medina-Franco José L

机构信息

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

Research Unit on Computational Biology and Drug Design, Children's Hospital of Mexico Federico Gomez, Mexico City 06720, Mexico.

出版信息

Pharmaceuticals (Basel). 2020 Dec 27;14(1):17. doi: 10.3390/ph14010017.

Abstract

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.

摘要

DNA甲基转移酶(DNMTs)抑制剂是表观遗传药物研发中颇具吸引力的化合物。它们也是用于理解表观遗传过程生物化学的化学工具。在此,我们报告了在酶抑制试验中鉴定出的五种不同的DNMT1抑制剂,这些抑制剂对DNMT3B无活性。得出的结论是,膳食成分茶黄素是DNMT1的抑制剂。另外两种新型DNMT1抑制剂是已获批的药物格列本脲和帕比司他。帕比司他是一种已知的组蛋白去乙酰化酶泛抑制剂,其对DNMT1的酶抑制活性与关于它在肝癌细胞系中降低DNMT1活性能力的实验报告一致。活性化合物与DNMT1的分子对接,以及使用最近开发的扩展连接相互作用特征方法重新评分,使得实验IC值与对接分数之间达成了极好的一致性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642a/7824300/ab69ff595742/pharmaceuticals-14-00017-g001.jpg

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