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be prevented by tetrodotoxin but not by the adrenergic antagonists timolol, yohimbine, or prazosin存储条件: Powder: -20°C
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to block Na(v)1.2, approximately 10 fold less potent to block tetrodotoxin-sensitive sodium (TTX-S Na(+)) currents
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05089771 | tetrodotoxin | PF 05089771 Tosylate | Na+ channels | Inhibitor相关产品: Orphenadrine hydrochloride | ProTx-III
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去极化。也曾作为 KCNQ 抑制剂用于研究河豚毒素(TTX)存在时小鼠胆碱能中间神经元(ChIs)膜电位超射/欠射的离子机制。中文名:XE-991英文名:XE-991中文别名:XE 991|10,10-双(4-萘甲基)-9(10H)-蒽酮英文
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by IL-6, IFN-α, and IFN-γ[1]. Dehydrocrenatidine reduces tetrodotoxin-resistant and sensitive voltage-gated sodium channel
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通道阻滞剂。Nav1.8是一种抗河豚毒素(TTX-R)钠离子通道,通过在周围感觉神经元中传递疼痛刺激而产生痛觉;A-803467通过阻滞该通道,能够对多种模型产生不同程度的疼痛减轻作用。A-803467已被用于进一步探究Nav1.8在传递
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, tetrodotoxin, quinone, macrolide antibiotics and modified sugars.
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| pain | PF 05089771 | tetrodotoxin相关产品: KT-362 fumarate | Strictosamide | Butamben | Halofuginone | PF 05089771 tosylate
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both fast tetrodotoxin-sensitive (TTX-S) and the slow tetrodotoxin-resistant (TTX-R) sodium currents in a dose-dependent
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?The PLD response induced by 1 mM L-CSA is not significantly decreased in the presence of 1 uM tetrodotoxin, suggesting