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Synthesis of lysine methyltransferase inhibitors
Lysine methyltransferase which catalyze methylation of histone and non-histone proteins, play a crucial role in diverse biological processes and has emerged as a promising target for the development of various human diseases, including cancer, inflammation, and psychiatric disorders. However, inhibi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511967/ https://www.ncbi.nlm.nih.gov/pubmed/26258118 http://dx.doi.org/10.3389/fchem.2015.00044 |
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author | Hui, Chunngai Ye, Tao |
author_facet | Hui, Chunngai Ye, Tao |
author_sort | Hui, Chunngai |
collection | PubMed |
description | Lysine methyltransferase which catalyze methylation of histone and non-histone proteins, play a crucial role in diverse biological processes and has emerged as a promising target for the development of various human diseases, including cancer, inflammation, and psychiatric disorders. However, inhibiting lysine methyltransferases selectively has presented many challenges to medicinal chemists. During the past decade, lysine methyltransferase inhibitors covering many different structural classes have been designed and developed. In this review, we describe the development of selective, small-molecule inhibitors of lysine methyltransferases with an emphasis on their discovery and chemical synthesis. We highlight the current state of lysine methyltransferase inhibitors and discuss future directions and opportunities for lysine methyltransferase inhibitor discovery. |
format | Online Article Text |
id | pubmed-4511967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45119672015-08-07 Synthesis of lysine methyltransferase inhibitors Hui, Chunngai Ye, Tao Front Chem Chemistry Lysine methyltransferase which catalyze methylation of histone and non-histone proteins, play a crucial role in diverse biological processes and has emerged as a promising target for the development of various human diseases, including cancer, inflammation, and psychiatric disorders. However, inhibiting lysine methyltransferases selectively has presented many challenges to medicinal chemists. During the past decade, lysine methyltransferase inhibitors covering many different structural classes have been designed and developed. In this review, we describe the development of selective, small-molecule inhibitors of lysine methyltransferases with an emphasis on their discovery and chemical synthesis. We highlight the current state of lysine methyltransferase inhibitors and discuss future directions and opportunities for lysine methyltransferase inhibitor discovery. Frontiers Media S.A. 2015-07-23 /pmc/articles/PMC4511967/ /pubmed/26258118 http://dx.doi.org/10.3389/fchem.2015.00044 Text en Copyright © 2015 Hui and Ye. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Hui, Chunngai Ye, Tao Synthesis of lysine methyltransferase inhibitors |
title | Synthesis of lysine methyltransferase inhibitors |
title_full | Synthesis of lysine methyltransferase inhibitors |
title_fullStr | Synthesis of lysine methyltransferase inhibitors |
title_full_unstemmed | Synthesis of lysine methyltransferase inhibitors |
title_short | Synthesis of lysine methyltransferase inhibitors |
title_sort | synthesis of lysine methyltransferase inhibitors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511967/ https://www.ncbi.nlm.nih.gov/pubmed/26258118 http://dx.doi.org/10.3389/fchem.2015.00044 |
work_keys_str_mv | AT huichunngai synthesisoflysinemethyltransferaseinhibitors AT yetao synthesisoflysinemethyltransferaseinhibitors |