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  • 抑制剂&激动剂
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    TargetMol | Inhibitors_Agonists
  • Mepivacaine
    甲哌卡因, Carbocaine
    T2236196-88-8
    Mepivacaine (Carbocaine) 是一种可用于局部麻醉的酰胺类化合物,可使人或动物短暂的失去自知觉。Mepivacaine 通过与神经细胞膜上特定的电压门控钠离子通道结合,抑制钠离子内流和膜去极化来发挥作用。Mepivacaine 适用于神经阻滞和硬膜外麻醉。
    • ¥ 115
    In stock
    规格
    数量
  • Mepivacaine hydrochloride
    Mepivacaine HCl, 盐酸甲哌卡因
    T09461722-62-9
    Mepivacaine hydrochloride (Mepivacaine HCl) 是具有局部麻醉特性的酰胺衍生物。Mepivacaine hydrochloride 与神经元细胞膜上特定的电压门控钠离子通道结合,抑制钠离子内流和膜去极化。
    • ¥ 143
    In stock
    规格
    数量
  • Dexivacaine
    BRN-0211230,Dexivacaina,BRN0211230,L(+)-Mepivacaine,BRN 0211230
    T3140024358-84-7
    Dexivacaine is an type of anesthetic.
    • ¥ 594
    5日内发货
    规格
    数量
  • Articaine hydrochloride
    Ultracaine, 阿替卡因, Articaine HCl, 盐酸阿替卡因, Hoe-045
    T213123964-57-0
    Articaine hydrochloride (Hoe-045) 一种牙科局部麻醉剂。
    • ¥ 133
    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