荧光
荧光各向异性
变构调节
分子
化学
小分子
亲缘关系
立体化学
晶体结构
结晶学
生物化学
受体
有机化学
量子力学
物理
作者
Ana S. Newton,Luca Deiana,D.E. Puleo,José A. Cisneros,Kara J. Cutrona,Joseph Schlessinger,William L. Jorgensen
标识
DOI:10.1021/acsmedchemlett.7b00154
摘要
A competitive fluorescence polarization (FP) assay is reported for determining binding affinities of probe molecules with the pseudokinase JAK2 JH2 allosteric site. The syntheses of the fluorescent 5 and 6 used in the assay are reported as well as Kd results for 10 compounds, including JNJ7706621, NVP-BSK805, and filgotinib (GLPG0634). X-ray crystal structures of JAK2 JH2 in complex with NVP-BSK805, filgotinib, and diaminopyrimidine 8 elucidate the binding poses.
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