Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22361 |
Mepivacaine
Carbocaine |
Sodium Channel | Membrane transporter/Ion channel |
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。 | |||
T0946 |
Mepivacaine hydrochloride
Mepivacaine HCl,盐酸甲哌卡因 |
Sodium Channel | Membrane transporter/Ion channel |
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。 | |||
T31400 |
Dexivacaine
BRN-0211230,Dexivacaina,BRN0211230,L(+)-Mepivacaine,BRN 0211230 |
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Dexivacaine is an type of anesthetic. | |||
T2131 |
Articaine hydrochloride
Ultracaine,盐酸阿替卡因,阿替卡因,Articaine HCl,Hoe-045 |
Sodium Channel | Membrane transporter/Ion channel |
Articaine hydrochloride (Hoe-045) 一种牙科局部麻醉剂。 | |||
T70538 |
PD-85639
|
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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 membr... |