Recent progress in the discovery of adenosine A(2A) receptor antagonists for the treatment of Parkinson's disease.

Unmesh Shah, Robert Hodgson
{"title":"Recent progress in the discovery of adenosine A(2A) receptor antagonists for the treatment of Parkinson's disease.","authors":"Unmesh Shah,&nbsp;Robert Hodgson","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Antagonism of the adenosine A2A receptor has emerged as a promising non-dopaminergic approach for the potential treatment of Parkinson's disease (PD). Several pharmaceutical and academic institutions have ongoing research programs in this area, and orally efficacious A2A receptor antagonists have been advanced into clinical development. Traditionally, antagonists of the A2A receptor are classified as xanthine and non-xanthine derivatives. This review provides a detailed summary of the recent SAR development that has led to the discovery of promising non-xanthine-based A2A receptor antagonists. The current clinical status and the potential utility of A2A receptor antagonists in indications other than PD are also discussed.</p>","PeriodicalId":10809,"journal":{"name":"Current opinion in drug discovery & development","volume":"13 4","pages":"466-80"},"PeriodicalIF":0.0000,"publicationDate":"2010-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in drug discovery & development","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Antagonism of the adenosine A2A receptor has emerged as a promising non-dopaminergic approach for the potential treatment of Parkinson's disease (PD). Several pharmaceutical and academic institutions have ongoing research programs in this area, and orally efficacious A2A receptor antagonists have been advanced into clinical development. Traditionally, antagonists of the A2A receptor are classified as xanthine and non-xanthine derivatives. This review provides a detailed summary of the recent SAR development that has led to the discovery of promising non-xanthine-based A2A receptor antagonists. The current clinical status and the potential utility of A2A receptor antagonists in indications other than PD are also discussed.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
治疗帕金森病的腺苷A(2A)受体拮抗剂的最新发现进展。
腺苷A2A受体的拮抗已成为治疗帕金森病(PD)的一种有前途的非多巴胺能方法。一些制药和学术机构正在进行这一领域的研究项目,口服有效的A2A受体拮抗剂已经进入临床开发。传统上,A2A受体拮抗剂分为黄嘌呤和非黄嘌呤衍生物。这篇综述提供了最近SAR发展的详细总结,导致了有前途的非黄嘌呤为基础的A2A受体拮抗剂的发现。本文还讨论了A2A受体拮抗剂在PD以外适应症中的临床现状和潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊最新文献
The role of the mTOR pathway in regulating food intake. The role of tau kinases in Alzheimer's disease. Current understanding and importance of histone phosphorylation in regulating chromatin biology. Network biology as a new approach to drug discovery. Conformational ensembles, signal transduction and residue hot spots: application to drug discovery.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1