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The Future of Medicinal Chemistry, PROTAC, and Undruggable Drug Targets
WRD5 is a promising target for anticancer drug discovery. In addition, it plays a vital role in epigenetic regulation. Since biological inactivation of WRD5 is difficult to reach via classical approach, PROTACs (Proteolysis Targeting Chimeras) are offering a new option. In a study, published in this...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389887/ https://www.ncbi.nlm.nih.gov/pubmed/34296872 http://dx.doi.org/10.1021/acs.jmedchem.1c01126 |
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author | Poso, Antti |
author_facet | Poso, Antti |
author_sort | Poso, Antti |
collection | PubMed |
description | WRD5 is a promising target for anticancer drug discovery. In addition, it plays a vital role in epigenetic regulation. Since biological inactivation of WRD5 is difficult to reach via classical approach, PROTACs (Proteolysis Targeting Chimeras) are offering a new option. In a study, published in this journal, new WRD5 targeting PROTACS are introduced. These new compounds, which are also active in cells, make it possible to evaluate the value of WRD5 as a drug target. |
format | Online Article Text |
id | pubmed-8389887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83898872021-08-31 The Future of Medicinal Chemistry, PROTAC, and Undruggable Drug Targets Poso, Antti J Med Chem WRD5 is a promising target for anticancer drug discovery. In addition, it plays a vital role in epigenetic regulation. Since biological inactivation of WRD5 is difficult to reach via classical approach, PROTACs (Proteolysis Targeting Chimeras) are offering a new option. In a study, published in this journal, new WRD5 targeting PROTACS are introduced. These new compounds, which are also active in cells, make it possible to evaluate the value of WRD5 as a drug target. American Chemical Society 2021-07-23 2021-08-12 /pmc/articles/PMC8389887/ /pubmed/34296872 http://dx.doi.org/10.1021/acs.jmedchem.1c01126 Text en © 2021 The Author. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Poso, Antti The Future of Medicinal Chemistry, PROTAC, and Undruggable Drug Targets |
title | The Future of Medicinal
Chemistry, PROTAC, and Undruggable
Drug Targets |
title_full | The Future of Medicinal
Chemistry, PROTAC, and Undruggable
Drug Targets |
title_fullStr | The Future of Medicinal
Chemistry, PROTAC, and Undruggable
Drug Targets |
title_full_unstemmed | The Future of Medicinal
Chemistry, PROTAC, and Undruggable
Drug Targets |
title_short | The Future of Medicinal
Chemistry, PROTAC, and Undruggable
Drug Targets |
title_sort | future of medicinal
chemistry, protac, and undruggable
drug targets |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389887/ https://www.ncbi.nlm.nih.gov/pubmed/34296872 http://dx.doi.org/10.1021/acs.jmedchem.1c01126 |
work_keys_str_mv | AT posoantti thefutureofmedicinalchemistryprotacandundruggabledrugtargets AT posoantti futureofmedicinalchemistryprotacandundruggabledrugtargets |