期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 51, 期 22, 页码 7049-7052出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm801050k
关键词
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A series of arylaminobenzimidazoles was designed and synthesized as Raf kinase inhibitors. Exploration of the structure-activity relationship resulted in compounds that are potent in vitro and show desirable in vivo properties.
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