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[来自蜘蛛白额高脚蛛毒液的谷氨酸受体拮抗剂]

[Glutamate receptor antagonists from the spider Argiope lobata venom].

作者信息

Grishin E V, Volkova T M, Arsen'ev A S

出版信息

Bioorg Khim. 1988 Jul;14(7):883-92.

PMID:2847758
Abstract

Homologous low molecular weight compounds blocking postsynaptic glutamate receptors were isolated from the Argiope lobata spider venom by ion-exchange chromatography and reverse-phase HPLC. Structures of nine different blocking agents were determined by NMR and mass spectroscopy. They can be divided into three groups: argiopin, argiopinins and pseudoargiopinines. The major principles of the structural organization of the novel class of antagonists of glutamate receptors were considered.

摘要

通过离子交换色谱法和反相高效液相色谱法,从大腹园蛛毒液中分离出了阻断突触后谷氨酸受体的同源低分子量化合物。通过核磁共振和质谱法确定了九种不同阻断剂的结构。它们可分为三组:蛛毒平、蛛毒平宁和假蛛毒平宁。探讨了这类新型谷氨酸受体拮抗剂结构组织的主要原理。

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1
[Glutamate receptor antagonists from the spider Argiope lobata venom].[来自蜘蛛白额高脚蛛毒液的谷氨酸受体拮抗剂]
Bioorg Khim. 1988 Jul;14(7):883-92.
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[Structural-functional characteristics of argiopine--the ion channel blockers from the spider Argiope lobata venom].[来自蜘蛛棒络新妇毒液的离子通道阻滞剂精氨酸平的结构功能特性]
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Isolation and structure analysis of components from venom of the spider Argiope lobata.横纹金蛛毒液成分的分离与结构分析
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New antagonists of glutamate receptors.
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[Action of the venom of the spider Argiope lobata on glutamatergic and cholinergic synapses].[蜘蛛银斑蛛毒液对谷氨酸能和胆碱能突触的作用]
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Slowly-reversible block of glutamate receptor-channels by venoms of the spiders, Argiope trifasciata and Araneus gemma.
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