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中枢烟碱样受体配体与药效基团。

Central nicotinic receptor ligands and pharmacophores.

作者信息

Glennon R A, Dukat M

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Virginia Commonwealth University, Richmond 23298-0540, USA.

出版信息

Pharm Acta Helv. 2000 Mar;74(2-3):103-14. doi: 10.1016/s0031-6865(99)00022-9.

Abstract

Multiple populations of pentameric nicotinic acetylcholinergic (nACh) receptors exist and several may be classified as central or neuronal. Neuronal nACh receptors, however, are primarily of the alpha 4 beta 2 and alpha 7 types, and these have been the focus of most recent investigations aimed at the development of novel agents and identification of pharmacophores. Selectivity data are limited. Furthermore, because several populations of nACh receptors might indirectly influence a given functional effect, it is difficult to discuss structure-activity relationships (SAR) in terms of differential SAR, or to formulate SAR on the basis of functional studies. For the most part, studies are limited to the formulation of structure-affinity relationships (SAFIR) for the binding of agents at nACh receptors, and for these the alpha 4 beta 2 population has been the most extensively investigated. SAFIR and newer agents are reviewed here with reference to earlier studies. Novel agents now have been identified that bind with up to 30 times higher affinity than nicotine and these are providing new insight into the understanding of nACh receptors.

摘要

存在多种五聚体烟碱型乙酰胆碱(nACh)受体群体,其中一些可归类为中枢型或神经元型。然而,神经元型nACh受体主要是α4β2和α7类型,这些一直是最近旨在开发新型药物和确定药效基团的研究重点。选择性数据有限。此外,由于几种nACh受体群体可能间接影响特定的功能效应,因此很难从差异构效关系的角度讨论构效关系(SAR),或者根据功能研究来制定SAR。在很大程度上,研究仅限于阐述药物与nACh受体结合的结构亲和力关系(SAFIR),其中α4β2群体是研究最广泛的。本文结合早期研究对SAFIR和新型药物进行了综述。现已鉴定出与尼古丁结合亲和力高达30倍的新型药物,这些药物为理解nACh受体提供了新的见解。

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