Design, Synthesis and Biological Evaluation of 6-(2,6-dichloro-3,5-dimethoxyphenyl)-4-Substituted-1H

来源 :2016年长三角药物化学研讨会 | 被引量 : 0次 | 上传用户:sisi22
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  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 is an urgent need in cancer treatment.Currently,several FGFR-selective inhibitors have progressed into clinical trials (Figure 1)[5-7].
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Phenanthridines,are an important class of nitrogen-containing compounds with a wide range of applications in material and medicinal chemistry1.Drugs with this ubiquitous scaffold (Figure 1) present br
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