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Identification of a novel histone H2A mono-ubiquitination-inhibiting cell-active small molecule.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2024 Jun 01; Vol. 105, pp. 129759. Date of Electronic Publication: 2024 Apr 16. - Publication Year :
- 2024
-
Abstract
- Histone H2A mono-ubiquitination plays important roles in epigenetic gene expression and is also involved in tumorigenesis. Small molecules controlling H2A ubiquitination are of interest as potential chemical tools and anticancer drugs. To identify novel small molecule inhibitors of H2A ubiquitination, we synthesized and evaluated several compounds designed based on PRT4165 (1), which is a reported histone ubiquitin ligase RING1A inhibitor. We found that compound 11b strongly inhibited the viability and reduced histone H2A mono-ubiquitination in human osteosarcoma U2OS cells. Therefore, compound 11b is a promising lead compound for the development of H2A histone ubiquitination-inhibiting small molecules.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024. Published by Elsevier Ltd.)
- Subjects :
- Humans
Cell Line, Tumor
Structure-Activity Relationship
Antineoplastic Agents pharmacology
Antineoplastic Agents chemistry
Antineoplastic Agents chemical synthesis
Molecular Structure
Cell Survival drug effects
Dose-Response Relationship, Drug
Histones metabolism
Ubiquitination drug effects
Small Molecule Libraries chemistry
Small Molecule Libraries pharmacology
Small Molecule Libraries chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 105
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 38636717
- Full Text :
- https://doi.org/10.1016/j.bmcl.2024.129759