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Design and synthesis of a novel series of N, 4-diphenylpyrimidin-2-amine derivatives as potent and selective PI3Kγ inhibitors

HL Yang, F Fang, CP Zhao, DD Li, JR Li, J Sun…

文献索引:Yang, Hua-Lin; Fang, Fei; Zhao, Chang-Po; Li, Dong-Dong; Li, Jing-Ran; Sun, Jian; Du, Qian-Ru; Zhu, Hai-Liang MedChemComm, 2014 , vol. 5, # 2 p. 219 - 225

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被引用次数: 1

摘要

Due to the increasing evidence linking the PI3Kγ pathway to various disease states, PI3Kγ is becoming an important target for cancer treatment. Herein we designed and synthesized a novel series of N, 4-diphenylpyrimidin-2-amine derivatives with low CDOCKER_INTERACTION_ENERGY and then evaluated their PI3Kγ in vitro inhibitory activities and in vitro antiproliferation assays against four human cancer cells. Among the ...