Small-Molecule Cyanamide Pan-TEADmiddotYAP1 Covalent Antagonists

被引:16
作者
Bum-Erdene, Khuchtumur [1 ]
Yeh, I-Ju [1 ]
Gonzalez-Gutierrez, Giovanni [2 ]
Ghozayel, Mona K. [1 ]
Pollok, Karen [3 ]
Meroueh, Samy O. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[2] Indiana Univ Bloomington, Dept Mol & Cellular Biochem, Bloomington, IN 47405 USA
[3] Indiana Univ Sch Med, Indiana Univ, Herman Wells Ctr Pediat Res B, Dept Pediat,Simon Canc Ctr, Indianapolis, IN 46202 USA
关键词
YAP; TEAD; GROWTH; INDUCTION; STABILITY; COMPONENT; BINDING; YORKIE;
D O I
10.1021/acs.jmedchem.2c01189
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Transcriptional enhanced associate domains (TEADs) are transcription factors that bind to cotranscriptional activators like the yes-associated protein (YAP) or its paralog transcriptional coactivator with a PDZ-binding motif (TAZ). TEAD center dot YAP/TAZ target genes are involved in tissue and immune homeostasis, organ size control, tumor growth, and metastasis. Here, we report isoindoline and octahydroisoindole small molecules with a cyanamide electrophile that forms a covalent bond with a conserved cysteine in the TEAD palmitate-binding cavity. Time-and concentration-dependent studies against TEAD1-4 yielded second-order rate constants kinact/KI greater than 100 M-1 s-1. Compounds inhibited YAP1 binding to TEADs with submicromolar IC50 values. Cocrystal structures with TEAD2 enabled structure-activity relationship studies. In mammalian cells, compounds suppressed CTGF mRNA levels and inhibited TEAD1-4 transcriptional activity with submicromolar IC50 values. Inhibition of TEAD binding to YAP1 in mammalian cells was also observed. Several compounds inhibited the cell viability of sarcoma, hepatocellular carcinoma, glioblastoma, and breast cancer cells with single-digit micromolar IC50 values.
引用
收藏
页码:266 / 284
页数:19
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