双环分子
磷脂酰肌醇
激酶
药物发现
药理学
生物化学
化学
立体化学
生物
作者
Koji Ochiai,Shigeki Seto,Masanobu Yajima,Ryosuke Namie,Noriaki Hashimoto,Motomichi Fujita,Akinobu Yokoyama,Takahiro Suezawa,Hitomi Matsui,Satoshi Tomizawa,Yuji Ishibashi,Yuta Tanaka,Miho Yajima,Michiaki Nagasawa,N Ando
标识
DOI:10.1021/acsmedchemlett.4c00090
摘要
Phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) is generated by phosphatidylinositol 4-phosphate 5-kinases (PIP5Ks) from phosphatidylinositol 4-phosphate (PI4P). Structurally diverse and selective inhibitors against PIP5Ks are required to further elucidate the therapeutic potential for PIP5K inhibition, although the effects of PIP5K inhibition on various diseases and their symptoms, such as cancer and chronic pain, have been reported. Our medicinal chemistry efforts led to novel and potent PIP5K1C inhibitors. Compounds 30 and 33 not only showed potent activity but also demonstrated low total clearance in mice and high levels of kinase selectivity. These compounds might serve as tools to further elucidate the complex biology and therapeutic potential of PIP5K inhibition.
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