化学
背景(考古学)
基因亚型
激酶
选择性
调制(音乐)
结构-活动关系
药理学
计算生物学
生物化学
组合化学
体外
基因
生物
催化作用
古生物学
哲学
美学
作者
Scott Boyd,Joanna Brookfield,Susan E. Critchlow,Iain Cumming,Nicola J. Curtis,J.E. Debreczeni,Sébastien L. Degorce,Craig S. Donald,Nicola J. Evans,Sam D. Groombridge,Philip Hopcroft,Neil P. Jones,Jason G. Kettle,Scott G. Lamont,Hilary Lewis,P. MacFaull,Sheila B. McLoughlin,Laurent Rigoreau,James M. Smith,Stephen A. St-Gallay
标识
DOI:10.1021/acs.jmedchem.5b00352
摘要
A weak screening hit with suboptimal physicochemical properties was optimized against PFKFB3 kinase using critical structure-guided insights. The resulting compounds demonstrated high selectivity over related PFKFB isoforms and modulation of the target in a cellular context. A selected example demonstrated exposure in animals following oral dosing. Examples from this series may serve as useful probes to understand the emerging biology of this metabolic target.
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