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Updated: May 20, 2026

Utilizing Thermal Shift Assay to Probe Substrate Binding to Selenoprotein O
Published on: August 9, 2024
Discovery of selenium-containing amino acid derivatives as novel ENL YEATS domain inhibitors via AlphaScreen-based
Siqi Guo1, Jianhao Li2, Yongxing Tao3
1College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Abstract:
Eleven-Nineteen-Leukemia Protein (ENL), a member of YEATS domain family, is a novel reader of lysine acetylation. Its deregulation is linked to various human diseases, especially cancer. Therefore, ENL has garnered significant interest as a potential therapeutic target. Herein, we report the discovery of novel ENL YEATS domain inhibitors via high-throughput screening. Hit compounds DC_E35 and DC_E36 were identified and structurally optimized, yielding the potent derivative DC_E35_5d (IC50 = 62.0 ± 14.7 nM). Biophysical assays confirmed direct target engagement. In MOLM-13 cells, DC_E35_5d reduced ENL thermal stability, downregulated the oncogene MYC, and synergized with the Bromodomain inhibitor JQ-1 to suppress cell growth. Hence, DC_E35_5d represents a novel class of ENL YEATS domain inhibitors with novel scaffold and has broad prospects for being a probe for ENL-related academic and clinical research.

