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首页> 外文期刊>Molecular pharmacology. >Rational Engineering Defines a Molecular Switch That Is Essential for Activity of Spider-Venom Peptides against the Analgesics Target NaV1.7
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Rational Engineering Defines a Molecular Switch That Is Essential for Activity of Spider-Venom Peptides against the Analgesics Target NaV1.7

机译:Rational Engineering定义了一种分子开关,对于对镇痛药靶NAV1.7的蜘蛛毒液肽的活性至关重要

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摘要

Many spider-venom peptides are known to modulate the activity of the voltage-gated sodium (NaV) subtype 1.7 (NaV1.7) channel, which has emerged as a promising analgesic target. In particular, a class of spider-venom peptides (NaSpTx1) has been found to potently inhibit NaV1.7 (nanomolar IC50), and has been shown to produce analgesic effects in animals
机译:已知许多蜘蛛 - 毒液肽调节电压门控钠(NAV)亚型1.7(NAV1.7)通道的活性,其被出现为有前途的镇痛靶。 特别地,已经发现一类蜘蛛毒液肽(NASPTX1)效果抑制Nav1.7(Nanomolar IC50),并且已被证明在动物中产生镇痛作用

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