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产品名称 | Sodium Channel ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Tolperisone HCl | ✔ | 99% | |||||||||||||||||
Lamotrigine | ✔ | 98% | |||||||||||||||||
Vinpocetine | ✔ | 98% | |||||||||||||||||
Zonisamide | ✔ | 99% | |||||||||||||||||
Dronedarone HCl | ✔ | 95% | |||||||||||||||||
Procainamide HCl | ✔ | 99% | |||||||||||||||||
Bupivacaine HCl | ✔ | 99+% | |||||||||||||||||
Benzocaine | ✔ | 98% | |||||||||||||||||
Carbamazepine |
++
Sodium channel, IC50: 131 μM |
98% | |||||||||||||||||
Quinidine sulfate dihydrate | ✔ | 98% | |||||||||||||||||
Ibutilide fumarate | ✔ | 99%+ | |||||||||||||||||
Dibucaine HCl | ✔ | 99+% | |||||||||||||||||
Mexiletine HCl | ✔ | 99% | |||||||||||||||||
Phenytoin | ✔ | 99+% | |||||||||||||||||
Camostat Mesylate |
+++
epithelial sodium channel (ENaC), IC50: 50 nM |
99%+ | |||||||||||||||||
Levobupivacaine | ✔ | 97+% | |||||||||||||||||
Oxcarbazepine |
+
sodium channel, IC50: 160 μM |
98% | |||||||||||||||||
Ambroxol | 98+% | ||||||||||||||||||
Primidone | ✔ | 99% | |||||||||||||||||
Propafenone | ✔ | 99% | |||||||||||||||||
A-803467 |
++++
Na(V1.8) channel, IC50: 8 nM |
99%+ | |||||||||||||||||
Rufinamide | ✔ | 99% | |||||||||||||||||
Phenytoin sodium | ✔ | 98% | |||||||||||||||||
Proparacaine HCl |
+
Voltage-gated sodium channel, ED50: 3.4 mM |
98+% | |||||||||||||||||
Riluzole | ✔ | 97% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | AZ194 is a pioneering, orally administered inhibitor that disrupts the CRMP2-Ubc9 interaction and inhibits NaV1.7 with an IC50 of 1.2 µM. It prevents the SUMOylation of CRMP2, effectively decreasing the amount of NaV1.7 expressed on the cell surface and provides antinociceptive effects[1]. |
Animal study | AZ194 offers pain relief in rat models of chemotherapy-induced and nerve injury-induced neuropathic pain. Administered orally at doses of 2 and 10 mg/kg, AZ194 restores mechanical sensitivity in animals experiencing neuropathic nociception from these conditions[1].AZ194, given at 10 mg/kg intraperitoneally to CD1 male mice, does not impact motor performance in an open field test. It enhances the efficacy of commonly used painkillers and activates NaV1.7-dependent endogenous opioid signaling[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.76mL 0.35mL 0.18mL |
8.81mL 1.76mL 0.88mL |
17.62mL 3.52mL 1.76mL |
CAS号 | 2241651-99-8 |
分子式 | C34H31F2N3O3 |
分子量 | 567.63 |
SMILES Code | O=C(C1=CC=C(OCC=2C=CC=C(F)C2)C(OC)=C1)N3CCC(C4=NC=5C=CC=CC5N4CC=6C=CC=C(F)C6)CC3 |
MDL No. | N/A |
别名 | |
运输 | 蓝冰 |
InChI Key | HDKZBBHJFURFLF-UHFFFAOYSA-N |
Pubchem ID | 135290226 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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