Discovery of novel hedgehog antagonists from cell-based screening: Isosteric modification of p38 bisamides as potent inhibitors of SMO.
作者:
主题词
酰胺类(Amides);动物(Animals);药物评价, 临床前(Drug Evaluation, Preclinical);猬蛋白质类(Hedgehog Proteins);小鼠(Mice);丝裂原活化蛋白激酶14(Mitogen-Activated Protein Kinase 14);分子结构(Molecular Structure);蛋白激酶抑制剂(Protein Kinase Inhibitors);受体, G-蛋白偶联(Receptors, G-Protein-Coupled);信号传导(Signal Transduction);构效关系(Structure-Activity Relationship)
DOI
10.1016/j.bmcl.2012.04.104
PMID
22704236
发布时间
2012-07-03
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