The design and synthesis of the high efficacy, non-peptide CCK1 receptor agonist PD 170292

被引:12
作者
Bernad, N
Burgaud, BGM
Horwell, DC
Lewthwaite, RA
Martinez, J
Pritchard, MC
机构
[1] Parke Davis Neurosci Res Ctr, Cambridge CB2 2QB, England
[2] CCIPE, Fac Pharm, F-34060 Montpellier, France
关键词
D O I
10.1016/S0960-894X(00)00198-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The design, synthesis and biological actions of a novel, non-peptide CCK1 receptor agonist (PD 170292) which exhibits a similar pharmacological profile to the CCK analogue JMV180 is reported. PD 170292 was designed based on a consideration of the structures of a peptide based CCK1 receptor selective agonist and a peptoid CCK2 receptor selective antagonist. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1245 / 1248
页数:4
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