PLK1
化学
Polo样激酶
激酶
小分子
药物发现
铅化合物
药理学
酶抑制剂
药品
药物开发
立体化学
组合化学
酶
生物化学
体外
细胞周期
细胞凋亡
医学
作者
Zhe Nie,Victoria A. Feher,Srinivasa Reddy Natala,Christopher M. McBride,Andre A. Kiryanov,Benjamin Jones,Betty Lam,Yan Liu,Stephen W. Kaldor,Jeffrey A. Stafford,Kouki Hikami,Noriko Uchiyama,Tomohiro Kawamoto,Yuichi Hikichi,Shin-ichi Matsumoto,Nobuyuki Amano,Lilly Zhang,David J. Hosfield,R.J. Skene,Hua Zou
标识
DOI:10.1016/j.bmcl.2013.02.083
摘要
Using structure-based drug design, we identified and optimized a novel series of pyrimidodiazepinone PLK1 inhibitors resulting in the selection of the development candidate TAK-960. TAK-960 is currently undergoing Phase I evaluation in adult patients with advanced solid malignancies.
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