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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Structure-activity relationship of Baifuzi-cerebrosides on BKCa channel activation
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Structure-activity relationship of Baifuzi-cerebrosides on BKCa channel activation

机译:白附子脑苷对BKCa通道激活的构效关系

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Our previous study reported that a mixture of cerebrosides from traditional Chinese medicine Baifuzi could activate BKCa channel. It is curious to know the effect of each single cerebroside on the channel. Here we isolated 5 pure cerebrosides from the mixture and determined their chemical structures. The most potent one increased the single channel open probability 6 folds with EC50 value of 1.0 μM. The structure-activity relationship revealed that acyl chain length of cerebrosides has potent effect, while configuration of double bond at C8-C9 on their long chain base has weak effect on the channel activity. Thus, this research provides a guide for design and synthesis of a lead cerebroside with more potent effect on the BKCa channel.
机译:我们以前的研究报告说,中药白附子的脑苷脂混合物可以激活BKCa通道。奇怪的是,知道每个单独的脑苷对通道的作用。在这里,我们从混合物中分离出5种纯脑苷,并确定了它们的化学结构。最有效的一种将单通道开放概率提高了6倍,EC50值为1.0μM。构效关系表明,脑苷脂的酰基链长度具有强效作用,而长链C8-C9处双键的构型对通道活性的影响较弱。因此,这项研究为设计和合成对BKCa通道具有更强效作用的脑铅酸铅提供了指南。

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