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Towards the design of ligands of the internal pocket TEADs C-terminal domain.

作者信息

Toulotte Florine, Coevoet Mathilde, Liberelle Maxime, Bailly Fabrice, Zagiel Benjamin, Gelin Muriel, Allemand Frédéric, Fourquet Patrick, Melnyk Patricia, Guichou Jean-François, Cotelle Philippe

机构信息

Univ Lille, INSERM, CHU Lille, UMR-S 1172, Lille Neuroscience and Cognition Research Center, F-59000, Lille, France.

Centre de Biologie Structurale (CBS), CNRS, INSERM, Univ Montpellier, F-34090, Montpellier, France.

出版信息

Eur J Med Chem. 2025 Jan 15;282:117026. doi: 10.1016/j.ejmech.2024.117026. Epub 2024 Nov 12.

DOI:10.1016/j.ejmech.2024.117026
PMID:39571457
Abstract

The Hippo pathway controls in organ size and tissue homeostasis through regulating cell growth, proliferation and apoptosis. Phosphorylation of the transcription co-activator YAP (Yes associated protein) and TAZ (Transcriptional coactivator with PDZ-binding motif) regulates their nuclear import and therefore their interaction with TEAD (Transcriptional Enhanced Associated Domain). YAP, TAZ and TEADs are dysregulated in several solid cancers making YAP/TAZ-TEAD interaction a new anti-cancer target. We identified by screening a small in-house library, 5-benzyloxindole which binds to hTEAD2 at its internal/palmitate pocket. Its optimization led to covalent inhibitors bearing different warhead. Soaking with hTEAD2 gave seven new crystal structures where the ligands occupied palmitate pocket. 5-Benzyloxyindoles armed with vinylsulfamide moiety inhibit YAP/TAZ-TEAD target genes expression and breast cancer cell proliferation at micromolar concentration.

摘要

相似文献

1
Towards the design of ligands of the internal pocket TEADs C-terminal domain.
Eur J Med Chem. 2025 Jan 15;282:117026. doi: 10.1016/j.ejmech.2024.117026. Epub 2024 Nov 12.
2
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Design, Synthesis and Evaluation of a Series of 1,5-Diaryl-1,2,3-triazole-4-carbohydrazones as Inhibitors of the YAP-TAZ/TEAD Complex.设计、合成及评价一系列 1,5-二芳基-1,2,3-三唑-4-甲酰肼类化合物作为 YAP-TAZ/TEAD 复合物抑制剂。
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