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作为AMPA受体拮抗剂的2,3-苯并二氮杂䓬类化合物的合成及其构效关系

Synthesis and structure-activity relationships of 2,3-benzodiazepines as AMPA receptor antagonists.

作者信息

Zappalà M, Grasso S, Micale N, Polimeni S, De Micheli C

机构信息

Dipartimento Farmaco-Chimico, Università di Messina, Viale Annunziata, 98168 Messina, Italy.

出版信息

Mini Rev Med Chem. 2001 Sep;1(3):243-53. doi: 10.2174/1389557013406783.

Abstract

There is increasing evidence of the potential therapeutic utility of glutamate receptor antagonists in the treatment of several neurodegenerative disorders, including stroke and epilepsy. In the last few years noncompetitive AMPA receptor antagonists have received considerable attention due to their therapeutic potentiality. The discovery of GYKI 52466, the prototype of noncompetitive AMPA receptor antagonists endowed with anticonvulsant and neuroprotective properties, induced growing interest on 2,3-benzodiazepine derivatives. This review covers the chemistry and pharmacology of this important class of AMPA receptor antagonists.

摘要

越来越多的证据表明,谷氨酸受体拮抗剂在治疗包括中风和癫痫在内的多种神经退行性疾病方面具有潜在的治疗效用。在过去几年中,非竞争性AMPA受体拮抗剂因其治疗潜力而受到了相当大的关注。非竞争性AMPA受体拮抗剂原型GYKI 52466的发现,其具有抗惊厥和神经保护特性,引发了人们对2,3-苯二氮䓬衍生物的越来越浓厚的兴趣。这篇综述涵盖了这类重要的AMPA受体拮抗剂的化学和药理学。

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