化学
药理学
计算生物学
药物发现
生物活性
结构-活动关系
药品
生物化学
苯衍生物
酶抑制剂
作者
Markus Vögtle,Holger Sellner,Emilie A. Chapeau,Pascal Furet,Bahaâ Salem,Mickaël Le Douget,Vincent Bordas,Jean-Marc Groell,Anne-Laure Le Goff,Christine Rouzet,Thomas Wietlisbach,Thomas Zimmermann,Joseph P. McKenna,Cara E. Brocklehurst,Patrick Chène,Markus Wartmann,Clemens Scheufler,Jörg Kallen,Kanter Ruben de,Stephanie Harlfinger
标识
DOI:10.1021/acs.jmedchem.5c03009
摘要
The interaction of transcriptional enhanced associate domain (TEAD) and transcriptional coactivator yes-associated protein (YAP) mediates oncogenic functions downstream of the Hippo pathway. In this report, we outline our efforts to find a potent inhibitor of this protein-protein interaction with suitable properties for clinical evaluation. We detail the medicinal chemistry program that led to the discovery of IAG933, an inhibitor with a balanced ADME profile, enabling its evaluation as a potential treatment option in clinical settings.
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