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抑制剂&激动剂
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TargetMol产品目录中 "tetracaine"的结果
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TargetMol产品目录中 "

tetracaine

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    TargetMol | Inhibitors_Agonists
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    TargetMol | Isotope_Products
  • Tetracaine hydrochloride
    盐酸丁卡因, Tetracaine HCl, Amethocalne HCl, Amethocaine hydrochloride
    T1198136-47-0
    Tetracaine hydrochloride (Amethocalne HCl) 是一种钙通道蛋白抑制剂,可阻断肌浆网中 Ca2+的电压敏感释放。它主要用作眼科的止痒剂和局部用药,可用于表面和脊髓麻醉。
    • ¥ 164
    In stock
    规格
    数量
  • Tetracaine-d6
    丁卡因-d6
    TMIJ-0246756771-02-5
    Tetracaine-d6 是 Tetracaine 的氘代化合物。Tetracaine 的 CAS 号为 94-24-6。
    • 待询
    20日内发货
    规格
    数量
  • Benzonatate
    苯佐那酯
    T19644104-31-4
    Benzonatate 是外周口服镇咳药,对咳嗽延伸受体 (cough stretch receptors) 的活性具有抑制作用。它是丁卡因样代谢物,能够阻断呼吸延伸受体的钠通道并产生局部麻醉作用。
    • ¥ 235
    In stock
    规格
    数量
  • PD-85639
    T70538149838-21-1
    PD-85639 is a voltage-gated sodium (Na+) channel blocker (75% in 10 min & >95% in 25 min blockage of Na+ current by 25 μM PD85,639; whole-cell patch clamp using primary rat brain neurons) that is shown to target rat brain Nav1.2 with simultaneous high- and low-affinity modes of binding (EC50 = 56 nM 40% & 20 μM 60% at pH 9.0, 5 nM 28% & 3 μM 72% at pH 7.4, against 2 nM [3H]-PD85,639 for binding rat brain synaptosomes; EC50 = 17 nM 39% & 10 μM 61% using at pH 9.0 using rat brain synaptosome membranes) and a fast kinetic (t1 2 = 1.2 at 4°C, <0.5 min at 25°C), competitive against the local anesthetic Na+ channel blockers tetracaine, bupivacaine, and mepivacaine, as well as Na+ channel activators veratridine and batrachotoxin (K1 = 0.26 μM against 5 nM [3H]-BTX for binding rat neocrotical membranes).
    • ¥ 10600
    6-8周
    规格
    数量
  • Anticancer agent 100
    T724412914922-73-7
    Anticancer agent 100 是一种丁卡因衍生物,具有抗癌活性,可用于癌症研究。
    • ¥ 10600
    6-8周
    规格
    数量
  • Anticancer agent 102
    T747672914922-86-2
    Anticancer agent 102 是丁卡因的衍生物。Anticancer agent 102 具有抗癌活性. Anticancer agent 102 诱导细胞凋亡。
    • 待询
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  • Anticancer agent 101
    T830952914922-80-6
    Anticanceragent 101,一种丁卡因衍生物,展现出抗癌活性。
    • 待询
    8-10周
    规格
    数量
  • Ent-(+)-Verticilide
    T863712056011-05-1
    ent-(+)-verticilide is an effective and specific inhibitor of cardiac ryanodine receptor (RyR2) calcium release channels, demonstrating antiarrhythmic properties. It suppresses RyR2-mediated diastolic Ca2+ leak and shows greater potency and a unique action mechanism compared to Dantrolene and Tetracaine. ent-(+)-verticilide serves as a valuable tool for exploring the therapeutic potential of addressing RyR2 hyperactivity in cardiac and neurological conditions [1].
    • 待询
    待询
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