治疗帕金森病的腺苷A(2A)受体拮抗剂的最新发现进展。

Unmesh Shah, Robert Hodgson
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引用次数: 0

摘要

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

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.

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