Discovery of Substituted 1H-Pyrazolo[3,4-b]pyridine Derivatives as Potent and Selective FGFR Kinase Inhibitors
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Design, Synthesis and Biological Evaluation of 6-(2,6-Dichloro-3,5-dimethoxyphenyl)-4-substituted-1H-indazoles as Potent Fibroblast Growth Factor Receptor Inhibitors.Magnetically separable graphene oxide anchored sulfonic acid: a novel, highly efficient and recyclable catalyst for one-pot synthesis of 3,6-di(pyridin-3-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitriles in deep eutectic solvent under microwave irradiat
P2860
Discovery of Substituted 1H-Pyrazolo[3,4-b]pyridine Derivatives as Potent and Selective FGFR Kinase Inhibitors
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Discovery of Substituted 1H-Py ...... lective FGFR Kinase Inhibitors
@en
type
label
Discovery of Substituted 1H-Py ...... lective FGFR Kinase Inhibitors
@en
prefLabel
Discovery of Substituted 1H-Py ...... lective FGFR Kinase Inhibitors
@en
P2093
P2860
P1476
Discovery of Substituted 1H-Py ...... lective FGFR Kinase Inhibitors
@en
P2093
Meiyu Geng
Wenhu Duan
Yiming Sun
P2860
P304
P356
10.1021/ACSMEDCHEMLETT.6B00066
P577
2016-04-20T00:00:00Z