INSERM, UMR-S 1172, Lille Neuroscience & Cognition, University of Lille, 59000, Lille, France.
Institut de Recherche en Cancérologie de Montpellier (IRCM), Institut Régional du Cancer de Montpellier (ICM), University of Montpellier, 208 rue des Apothicaires, 34298, Montpellier Cedex 5, France.
ChemMedChem. 2021 Sep 16;16(18):2823-2844. doi: 10.1002/cmdc.202100153. Epub 2021 Jul 1.
Starting from our previously reported hit, a series of 1,5-diaryl-1,2,3-triazole-4-carbohydrazones were synthesized and evaluated as inhibitors of the YAP/TAZ-TEAD complex. Their binding to hTEAD2 was confirmed by nanodifferential scanning fluorimetry, and some of the compounds were also found to moderately disrupt the YAP-TEAD interaction, as assessed by a fluorescence polarization assay. A TEAD luciferase gene reporter assay performed in HEK293T cells and RTqPCR measurements in MDA-MB231 cells showed that these compounds inhibit YAP/TAZ-TEAD activity to cells in the micromolar range. In spite of the cytotoxic effects displayed by some of the compounds of this series, they are still good starting points and can be suitably modified into an effective and viable YAP-TEAD disruptor in the future.
从我们之前报道的先导化合物出发,我们合成了一系列 1,5-二芳基-1,2,3-三唑-4-甲酰肼,并将其作为 YAP/TAZ-TEAD 复合物的抑制剂进行了评估。通过纳米差示扫描荧光法证实了它们与 hTEAD2 的结合,并且通过荧光偏振测定法还发现一些化合物可适度破坏 YAP-TEAD 相互作用。在 HEK293T 细胞中进行的 TEAD 荧光素酶基因报告基因测定和在 MDA-MB231 细胞中的 RTqPCR 测量表明,这些化合物以微摩尔范围抑制 YAP/TAZ-TEAD 对细胞的活性。尽管该系列的一些化合物显示出细胞毒性作用,但它们仍然是良好的起点,并且将来可以适当修饰成有效的可行的 YAP-TEAD 破坏剂。