VGSCs-IN-1
CAS No. 1204296-79-6
VGSCs-IN-1 ( —— )
产品货号. M37270 CAS No. 1204296-79-6
VGSCs-IN-1 (compound 14) 是 Riluzole (HY-B0211) 的 2-哌嗪类似物,是一种人电压门控钠通道 (VGSC) 抑制剂。VGSCs-IN-1 显示出良好的 Nav1.4 阻断活性。VGSCs-IN-1 的 pKa 为 7.6,cLog P 为 2.4。VGSCs-IN-1可用于细胞兴奋性障碍研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2157 | 有现货 |
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| 10MG | ¥3154 | 有现货 |
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| 25MG | ¥4864 | 有现货 |
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| 50MG | ¥6417 | 有现货 |
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| 100MG | ¥8568 | 有现货 |
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| 200MG | ¥11520 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称VGSCs-IN-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述VGSCs-IN-1 (compound 14) 是 Riluzole (HY-B0211) 的 2-哌嗪类似物,是一种人电压门控钠通道 (VGSC) 抑制剂。VGSCs-IN-1 显示出良好的 Nav1.4 阻断活性。VGSCs-IN-1 的 pKa 为 7.6,cLog P 为 2.4。VGSCs-IN-1可用于细胞兴奋性障碍研究。
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产品描述VGSCs-IN-1 (compound 14), a 2-piperazine analog of Riluzole (HY-B0211), is a human voltage-gated sodium channels (VGSCs) inhibitor. VGSCs-IN-1 shows great Nav1.4 blocking activity. VGSCs-IN-1 has a pKa of 7.6 and a cLog P of 2.4. VGSCs-IN-1 can be used for cell excitability disorders research.
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体外实验——
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体内实验——
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同义词——
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通路Membrane Transporter/Ion Channel
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靶点Sodium Channel
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受体Sodium Channel
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研究领域——
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适应症——
化学信息
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CAS Number1204296-79-6
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分子量303.3
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分子式C12H12F3N3OS
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纯度>98% (HPLC)
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溶解度——
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SMILESFC(F)(F)OC1=CC2=C(C=C1)N=C(S2)N1CCNCC1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Carbamazepine
卡马西平是一种钠通道阻滞剂,是一种抗惊厥化合物。
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Silperisone HCl
Silperisone HCl (RGH-5002) blocks sodium and calcium channels in cells, decreases excitability and contractility of muscle cells, reduces peripheral tone, and acts as a muscle relaxant and peripheral vasodilator. Silperisone HCl is used to treat recurrent painful myoclonus due to spinal cord injury, abnormal hypertonia due to cerebrovascular disease, dystonia symptoms, cone tension syndrome, multiple sclerosis myospasm and myelitis. silperisone is a sodium channel protein type 2 alpha channel blocker. silperisone is an organosilicon similar to tolperisone, an organosilicon compound with centrally acting muscle relaxant properties.
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APETx2
Acid-sensing ion channel 3 (ASIC3) channel blocker (IC50 values are 63 and 175 nM for homomeric rat and human ASIC3 channels). Also inhibits NaV1.8 and NaV1.2 channels (IC50 values are 55 and 114 nM respectively). Demonstrates analgesic properties against acid-induced and inflammatory pain.
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