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Discovery of a First-in-Class Inhibitor of the Histone Methyltransferase SETD2 Suitable for Preclinical Studies
[Image: see text] SET domain-containing protein 2 (SETD2), a histone methyltransferase, has been identified as a target of interest in certain hematological malignancies, including multiple myeloma. This account details the discovery of EPZ-719, a novel and potent SETD2 inhibitor with a high selecti...
Autores principales: | , , , , , , , , , , , , , , , , |
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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/PMC8521618/ https://www.ncbi.nlm.nih.gov/pubmed/34671445 http://dx.doi.org/10.1021/acsmedchemlett.1c00272 |
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author | Lampe, John W. Alford, Joshua S. Boriak-Sjodin, P. Ann Brach, Dorothy Cosmopoulos, Kat Duncan, Kenneth W. Eckley, Sean T. Foley, Megan A. Harvey, Darren M. Motwani, Vinny Munchhof, Michael J. Raimondi, Alejandra Riera, Thomas V. Tang, Cuyue Thomenius, Michael J. Totman, Jennifer Farrow, Neil A. |
author_facet | Lampe, John W. Alford, Joshua S. Boriak-Sjodin, P. Ann Brach, Dorothy Cosmopoulos, Kat Duncan, Kenneth W. Eckley, Sean T. Foley, Megan A. Harvey, Darren M. Motwani, Vinny Munchhof, Michael J. Raimondi, Alejandra Riera, Thomas V. Tang, Cuyue Thomenius, Michael J. Totman, Jennifer Farrow, Neil A. |
author_sort | Lampe, John W. |
collection | PubMed |
description | [Image: see text] SET domain-containing protein 2 (SETD2), a histone methyltransferase, has been identified as a target of interest in certain hematological malignancies, including multiple myeloma. This account details the discovery of EPZ-719, a novel and potent SETD2 inhibitor with a high selectivity over other histone methyltransferases. A screening campaign of the Epizyme proprietary histone methyltransferase-biased library identified potential leads based on a 2-amidoindole core. Structure-based drug design (SBDD) and drug metabolism/pharmacokinetics (DMPK) optimization resulted in EPZ-719, an attractive tool compound for the interrogation of SETD2 biology that enables in vivo target validation studies. |
format | Online Article Text |
id | pubmed-8521618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85216182021-10-19 Discovery of a First-in-Class Inhibitor of the Histone Methyltransferase SETD2 Suitable for Preclinical Studies Lampe, John W. Alford, Joshua S. Boriak-Sjodin, P. Ann Brach, Dorothy Cosmopoulos, Kat Duncan, Kenneth W. Eckley, Sean T. Foley, Megan A. Harvey, Darren M. Motwani, Vinny Munchhof, Michael J. Raimondi, Alejandra Riera, Thomas V. Tang, Cuyue Thomenius, Michael J. Totman, Jennifer Farrow, Neil A. ACS Med Chem Lett [Image: see text] SET domain-containing protein 2 (SETD2), a histone methyltransferase, has been identified as a target of interest in certain hematological malignancies, including multiple myeloma. This account details the discovery of EPZ-719, a novel and potent SETD2 inhibitor with a high selectivity over other histone methyltransferases. A screening campaign of the Epizyme proprietary histone methyltransferase-biased library identified potential leads based on a 2-amidoindole core. Structure-based drug design (SBDD) and drug metabolism/pharmacokinetics (DMPK) optimization resulted in EPZ-719, an attractive tool compound for the interrogation of SETD2 biology that enables in vivo target validation studies. American Chemical Society 2021-08-24 /pmc/articles/PMC8521618/ /pubmed/34671445 http://dx.doi.org/10.1021/acsmedchemlett.1c00272 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lampe, John W. Alford, Joshua S. Boriak-Sjodin, P. Ann Brach, Dorothy Cosmopoulos, Kat Duncan, Kenneth W. Eckley, Sean T. Foley, Megan A. Harvey, Darren M. Motwani, Vinny Munchhof, Michael J. Raimondi, Alejandra Riera, Thomas V. Tang, Cuyue Thomenius, Michael J. Totman, Jennifer Farrow, Neil A. Discovery of a First-in-Class Inhibitor of the Histone Methyltransferase SETD2 Suitable for Preclinical Studies |
title | Discovery of a First-in-Class Inhibitor of the Histone
Methyltransferase SETD2 Suitable for Preclinical Studies |
title_full | Discovery of a First-in-Class Inhibitor of the Histone
Methyltransferase SETD2 Suitable for Preclinical Studies |
title_fullStr | Discovery of a First-in-Class Inhibitor of the Histone
Methyltransferase SETD2 Suitable for Preclinical Studies |
title_full_unstemmed | Discovery of a First-in-Class Inhibitor of the Histone
Methyltransferase SETD2 Suitable for Preclinical Studies |
title_short | Discovery of a First-in-Class Inhibitor of the Histone
Methyltransferase SETD2 Suitable for Preclinical Studies |
title_sort | discovery of a first-in-class inhibitor of the histone
methyltransferase setd2 suitable for preclinical studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521618/ https://www.ncbi.nlm.nih.gov/pubmed/34671445 http://dx.doi.org/10.1021/acsmedchemlett.1c00272 |
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