Identification of small molecule agonists of the motilin receptor

被引:14
|
作者
Heightman, Tom D. [1 ]
Conway, Elizabeth [2 ]
Corbett, David F. [2 ]
Macdonald, Gregor J. [1 ]
Stemp, Geoffrey
Westaway, Susan M.
Celestini, Paolo [4 ]
Gagliardi, Stefania [4 ]
Riccaboni, Mauro [4 ]
Ronzoni, Silvano [4 ]
Vaidya, Kalindi [2 ]
Butler, Sharon [2 ]
Mckay, Fiona [2 ]
Muir, Alison [2 ]
Powney, Ben [2 ]
Winborn, Kim [2 ]
Wise, Alan [2 ]
Jarvie, Emma M. [1 ]
Sanger, Gareth J. [3 ]
机构
[1] GlaxoSmithKline, Neurol & GI Ctr Excellence Drug Discovery, Harlow CM19 5AW, Essex, England
[2] GlaxoSmithKline R&D, Mol Discovery Res, Harlow CM19 5AW, Essex, England
[3] GlaxoSmithKline, Med Res Ctr, Immunoinflammat Ctr Excellence Drug Discovery, Stevenage SG1 2NY, Herts, England
[4] NiKem Res Srl, I-20021 Baranzate Di Bollate, MI, Italy
关键词
Motilin; Receptor; Agonist; GPCR;
D O I
10.1016/j.bmcl.2008.10.071
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
High-throughput screening resulted in the identification of a series of novel motilin receptor agonists with relatively low molecular weights. The series originated from an array of biphenyl derivatives designed to target 7-transmembrane (7-TM) receptors. Further investigation of the structure-activity relationship within the series resulted in the identi. cation of compound (22) as a potent and selective agonist at the motilin receptor. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6423 / 6428
页数:6
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