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Discovery of a subtype-selective, covalent inhibitor against palmitoylation pocket of TEAD3
Acta Pharmaceutica Sinica B ; (6): 3206-3219, 2021.
Article in English | WPRIM (Western Pacific) | ID: wpr-922788
Responsible library: WPRO
ABSTRACT
The TEA domain (TEAD) family proteins (TEAD1‒4) are essential transcription factors that control cell differentiation and organ size in the Hippo pathway. Although the sequences and structures of TEAD family proteins are highly conserved, each TEAD isoform has unique physiological and pathological functions. Therefore, the development and discovery of subtype selective inhibitors for TEAD protein will provide important chemical probes for the TEAD-related function studies in development and diseases. Here, we identified a novel TEAD1/3 covalent inhibitor (DC-TEADin1072) with biochemical IC

Full text: Available Database: WPRIM (Western Pacific) Language: English Journal: Acta Pharmaceutica Sinica B Year: 2021 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Language: English Journal: Acta Pharmaceutica Sinica B Year: 2021 Document type: Article
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