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石房蛤毒素。

Saxitoxin.

机构信息

Department of Chemistry, Stanford University, Stanford, CA 94305-5080 (USA).

出版信息

Angew Chem Int Ed Engl. 2014 Jun 2;53(23):5760-84. doi: 10.1002/anie.201308235. Epub 2014 Apr 25.

Abstract

The paralytic agent (+)-saxitoxin (STX), most commonly associated with oceanic red tides and shellfish poisoning, is a potent inhibitor of electrical conduction in cells. Its nefarious effects result from inhibition of voltage-gated sodium channels (Na(V)s), the obligatory proteins responsible for the initiation and propagation of action potentials. In the annals of ion channel research, the identification and characterization of Na(V)s trace to the availability of STX and an allied guanidinium derivative, tetrodotoxin. The mystique of STX is expressed in both its function and form, as this uniquely compact dication boasts more heteroatoms than carbon centers. This Review highlights both the chemistry and chemical biology of this fascinating natural product, and offers a perspective as to how molecular design and synthesis may be used to explore Na(V) structure and function.

摘要

麻痹剂 (+)-石房蛤毒素(STX),最常见于海洋赤潮和贝类中毒,是一种有效的细胞电传导抑制剂。它的有害作用是由于抑制电压门控钠离子通道(Na(V)s)所致,Na(V)s 是负责产生和传播动作电位的必需蛋白。在离子通道研究的历史中,Na(V)s 的鉴定和特性可以追溯到 STX 和一种相关的胍基衍生物——河豚毒素的可用性。STX 的神秘之处在于它的功能和形式,因为这种独特的紧凑二价阳离子拥有比碳原子更多的杂原子。这篇综述强调了这种迷人天然产物的化学和化学生物学,并提供了一个视角,说明分子设计和合成如何用于探索 Na(V)的结构和功能。

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