Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo(1,2-b)pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.

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作者： Scott Sawyer J ^[1] ; Beight DW ; Britt KS ; Anderson BD ; Campbell RM ; Goodson T Jr ; Herron DK ; Li HY ; McMillen WT ; Mort N ; Parsons S ; Smith EC ; Wagner JR ; Yan L ; Zhang F ; Yingling JM

作者单位： Discovery Chemistry Research and Technology, The Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN 46285, USA. ^[1]

关键词 pyrazole Phosphotransferases receptor mitogen-activated protein kinase p38 磷酸转移酶类

发布时间 2013-11-20

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Bioorganic and Medicinal Chemistry Letters

2004年14卷13期

3581-3584页

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Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo(1,2-b)pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.

Bioorganic and Medicinal Chemistry Letters

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Bioorganic and Medicinal Chemistry Letters

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Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo(1,2-b)pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.

Bioorganic and Medicinal Chemistry Letters

相似文献

Bioorganic and Medicinal Chemistry Letters

相关期刊

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