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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Activation of human IK and SK Ca2+-activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)
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Activation of human IK and SK Ca2+-activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)

机译:NS309(6,7-dichloro-1H-indole-2,3-dione 3-oxime)激活人IK和SK Ca2 +激活的K +通道

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摘要

We have identified and characterized the compound NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime) as a potent activator of human Ca2+-activated K+ channels of SK and IK types, whereas it is devoid of effect on BK type channels. IK- and SK-channels have previously been reported to be activated by the benzimidazolinone, 1-EBIO and more potently by its dichloronated-analogue, DC-EBIO. NS309 is at least 1000 times more potent than 1-EBIO and at least 30 times more potent than DC-EBIO when the compounds are compared on the same cell. (C) 2004 Elsevier B.V. All rights reserved.
机译:我们已经确定并表征了化合物NS309(6,7-二氯-1H-吲哚-2,3-二酮3-肟)是人类Ca2 +激活的SK和IK类型K +通道的有效激活剂,但它没有对BK类型通道的影响。以前已经报道过IK和SK通道被苯并咪唑啉酮1-EBIO激活,更有效地是由其二氯代类似物DC-EBIO激活。当在同一细胞中比较化合物时,NS309的效力至少是1-EBIO的1000倍,效力是DC-EBIO的至少30倍。 (C)2004 Elsevier B.V.保留所有权利。

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