Hit-to-lead studies:: The discovery of potent adamantane amide P2X7 receptor antagonists

被引：115

作者：

Baxter, A ^{[1
]}

Bent, J ^{[1
]}

Bowers, K ^{[1
]}

Braddock, M ^{[1
]}

Brough, S ^{[1
]}

Fagura, M ^{[1
]}

Lawson, M ^{[1
]}

McInally, T ^{[1
]}

Mortimore, M ^{[1
]}

Robertson, M ^{[1
]}

Weaver, R ^{[1
]}

Webborn, P ^{[1
]}

机构：

[1] AStraZeneca R&D Charnwood, Loughborough LE11 5RH, Leics, England

来源：

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 2003年 / 13卷 / 22期

关键词：

D O I：

10.1016/j.bmcl.2003.08.034

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

A Hit-to-Lead optimisation programme was carried out on the adamantane high throughput screening hit I resulting in the discovery of a number of potent P2X(7) antagonists. (C) 2003 Elsevier Ltd. All rights reserved.

引用

页码：4047 / 4050

页数：4

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