Synthesis and SAR of 8-aza-quinoxalin-2(1H)-one as corticotropin-releasing factor-1 receptor antagonists

被引：0
|
作者：
Dasgupta, Bireshwar [1 ]
Dzierba, Carolyn D. [1 ]
Sielecki, Thais M. [1 ]
Galka, Amy [1 ]
Johnson, Tricia L. [1 ]
Takvorian, Amy G. [1 ]
Rafalski, Maria [1 ]
Kasireddy-Polam, Padmaja [1 ]
Vig, Shikha [1 ]
Arvanitis, Argyrios G. [1 ]
Zhang, Ge [2 ]
Molski, Thaddeus F. [2 ]
Zaczek, Robert C. [2 ]
Combs, Andrew P. [1 ]
Gilligan, Paul J. [1 ]
Trainor, George [4 ]
Bronson, Joanne J. [1 ]
Macor, John E. [3 ]
机构：
[1] Bristol Myers Squibb Co, Res & Dev, Neurosci Discovery Chem, Wallingford, CT 06492 USA
[2] Bristol Myers Squibb Co, Res & Dev, Neurosci Discovery Biol, Wallingford, CT 06492 USA
[3] Bristol Myers Squibb Co, Res & Dev, Neurosci Chem, Wallingford, CT 06492 USA
[4] Bristol Myers Squibb Co, Discovery Chem, Res & Dev, Princeton, NJ 08543 USA
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2009年 / 238卷
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中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
85-MEDI
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页数：1
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