三唑
化学
荧光素酶
HEK 293细胞
荧光
报告基因
细胞毒性T细胞
体外
组合化学
立体化学
生物化学
基因
转染
基因表达
物理
有机化学
量子力学
作者
Floriane Gibault,Manon Sturbaut,Mathilde Coevoet,Martine Pugnière,Ashley Burtscher,Frédéric Allemand,Patricia Melnyk,Wanjin Hong,Brian P. Rubin,Ajaybabu V. Pobbati,Jean‐François Guichou,Philippe Cotelle,Fabrice Bailly
出处
期刊:ChemMedChem
[Wiley]
日期:2021-05-25
卷期号:16 (18): 2823-2844
被引量:16
标识
DOI:10.1002/cmdc.202100153
摘要
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.
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