Structure–Activity Relationship Studies of DNA Methyltransferase 1 Monovalent Degraders

DNA methyltransferase 1 (DNMT1), which catalyzes maintenance methylation of hemimethylated DNA during DNA replication, is overexpressed in cancer. Recently, the first-in-class DNMT1-selective noncovalent small-molecule inhibitors, GSK3484862 and GSK3685032, were discovered. These inhibitors were also reported to degrade DNMT1. However, structure-activity relationship (SAR) studies of these monovalent DNMT1 degraders are lacking. Here, we report our SAR studies of this scaffold on degrading DNMT1, which led to the discovery of multiple lead degraders, including compound <b>4</b> (MS9024). Compound <b>4</b> potently and selectively degraded DNMT1 in multiple cancer cell lines in a concentration-, time-, and proteasome-dependent manner without altering DNMT1 transcription. Further mechanism-of-action studies suggest that the DNMT1 degradation induced by <b>4</b> was not mediated by lysosome or cullin RING E3 ligases but could potentially be mediated by HECT E3 ligases and/or UHRF1. Collectively, these studies pave the way for further developing DNMT1 monovalent degraders as potential therapeutics and useful chemical tools.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-02-05
DOI
https://doi.org/10.1021/acs.jmedchem.4c02161
Citations
5
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
4.03

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article

Structure–Activity Relationship Studies of DNA Methyltransferase 1 Monovalent Degraders

Scott B. Rothbart, H. Ümit Kanıskan, Xiaodong Cheng, Jian Jun Jin et al.
5 citations
Journal of Medicinal Chemistry
Epigenetics and DNA Methylation
4.03
article

Structure–Activity Relationship Studies of DNA Methyltransferase 1 Monovalent Degraders

Scott B. Rothbart, H. Ümit Kanıskan, Xiaodong Cheng, Jian Jun Jin, Jujun Zhou, Yan Xiong, Yue Zhong, Joel Hrit, Qin Chen, Xian Chen, Ling Xie, Youngeun Lee, Yulin Han, Chao Qian
article en
5 citations

Abstract

DNA methyltransferase 1 (DNMT1), which catalyzes maintenance methylation of hemimethylated DNA during DNA replication, is overexpressed in cancer. Recently, the first-in-class DNMT1-selective noncovalent small-molecule inhibitors, GSK3484862 and GSK3685032, were discovered. These inhibitors were also reported to degrade DNMT1. However, structure-activity relationship (SAR) studies of these monovalent DNMT1 degraders are lacking. Here, we report our SAR studies of this scaffold on degrading DNMT1, which led to the discovery of multiple lead degraders, including compound <b>4</b> (MS9024). Compound <b>4</b> potently and selectively degraded DNMT1 in multiple cancer cell lines in a concentration-, time-, and proteasome-dependent manner without altering DNMT1 transcription. Further mechanism-of-action studies suggest that the DNMT1 degradation induced by <b>4</b> was not mediated by lysosome or cullin RING E3 ligases but could potentially be mediated by HECT E3 ligases and/or UHRF1. Collectively, these studies pave the way for further developing DNMT1 monovalent degraders as potential therapeutics and useful chemical tools.

Journal of Medicinal ChemistryVol. 68(3)
University of North Carolina at Chapel Hill (US), Van Andel Institute (US), The University of Texas MD Anderson Cancer Center (US), Tisch Hospital (US), Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai (US)
NIH Office of the Director, National Cancer Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 7%
Epigenetics and DNA Methylation
4.03
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