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首页> 外文期刊>Current pharmaceutical design >Anticonvulsant sulfonamides/sulfamates/sulfamides with carbonic anhydrase inhibitory activity: drug design and mechanism of action.
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Anticonvulsant sulfonamides/sulfamates/sulfamides with carbonic anhydrase inhibitory activity: drug design and mechanism of action.

机译:具有碳酸酐酶抑制活性的抗惊厥性磺酰胺/磺酸盐/磺酰胺:药物设计和作用机理。

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摘要

The marketed antiepileptic drugs can not solve entirely the problem of seizure in patients suffering from refractory epilepsies. Therefore, new anticonvulsant compounds structurally and pharmacologically different of the currently prescribed drugs are needed. Carbonic anhydrase (CA) inhibitors are known to act as anticonvulsant since several decades while the link between CA and seizure is not straightforward. However, the recent discovery that several CA isozymes are expressed in brain and the better knowledge of their physiological/pathological role, lead to the emergence of new CA inhibitors with anticonvulsant effect including: analogues of acetazolamide, analogues of topiramate, aromatic or heterocyclic sulfonamides incorporating valproyl or adamantyl moieties. Different strategies are developed for the design of new more selective CA inhibitors with anticonvulsant properties.
机译:市售的抗癫痫药不能完全解决难治性癫痫患者的癫痫发作问题。因此,需要与当前处方药物在结构和药理上不同的新的抗惊厥化合物。数十年来,碳酸酐酶(CA)抑制剂可作为抗惊厥药,而CA与癫痫发作之间的联系并不直接。但是,最近发现几种CA同工酶在大脑中表达,并且对它们的生理/病理作用有了更深入的了解,导致出现了具有抗惊厥作用的新型CA抑制剂,包括:乙酰唑胺类似物,托吡酯类似物,芳香族或杂环磺酰胺类丙戊酰基或金刚烷基部分。针对具有抗惊厥特性的新型更具选择性的CA抑制剂的设计,开发了不同的策略。

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