论文部分内容阅读
新型嘧啶类BTK共价抑制剂的设计、合成及生物活性研究
【机 构】
：
中国药科大学药物科学研究院,南京,210009
【出 处】
：
2016年长三角药物化学研讨会
【发表日期】
：
2016年11期
其他文献
Design, synthesis and pharmacological evaluation of ANTA XV derivatives as Hedgehog signaling pathwa
会议
Stereoselective and Regioselective Preparations of C-Pentopyranosides and Formal Synthesis of Omarig
会议
Design, Synthesis and Biological Evaluation of 6-(2,6-dichloro-3,5-dimethoxyphenyl)-4-Substituted-1H
Tyrosine kinase fibroblast growth factor receptor (FGFR),which is aberrant in various cancer types,is a promising target for cancer therapy[1-4].Thus,discovery of potent and selective FGFR inhibitors
会议
Design, Synthesis, and Evaluation of Asymmetric EF24 Analogues as Potential Anti-Cancer Agents for L
The nuclear factor-kappa B (NF-κB) signaling pathway has been targeted for the therapy of various cancers,including lung cancer.EF24 was considered as a potent inhibitor of NF-κB signaling pathway.