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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
NN414
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
279215-43-9
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1925.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥1750.0 |
| 规格: | 10 mg | 产品价格: | ¥2800.0 |
| 规格: | 25 mg | 产品价格: | ¥5135.0 |
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Tifenazoxide
CAS No. : 279215-43-9
MCE 国际站:Tifenazoxide
产品活性:Tifenazoxide (NN414) 是一种有效的,口服活性的 SUR1/Kir6.2 选择性 KATP 通道开放剂。Tifenazoxide 具有抗糖尿病作用,可以抑制葡萄糖刺激的胰岛素在体内和体外的释放,并对葡萄糖稳态具有有益作用。
研究领域:Membrane Transporter/Ion Channel
作用靶点:Potassium Channel
In Vitro: Tifenazoxide (NN414) hyperpolarises βTC3 cell membranes, and inhibits insulin release from βTC6, from isolated rat islets and from human islets at least a 100-fold more potent than Diazoxide.
The EC50 values for Tifenazoxide and diazoxide are 0.45 and 31 µM, respectively in the patch-clamp assay. Tifenazoxide (100 µM) activates Kir6.2/SUR1 channels, but not Kir6.2/SUR2A or Kir6.2/SUR2 channels, expressed in Xenopus oocytes both in whole-cell and inside-out macropatch recordings.
Tifenazoxide is a potent inhibitor of glucose stimulated insulin release from βTC6 cells (IC50 = 0.15 µM).
In Vivo: Tifenazoxide (NN414; 1.5 mg/kg; oral administration; twice daily; for 3 weeks; male VDF Zucker (fa/fa) rat) treatment for 3 weeks in VDF rats reduces basal hyperglycemia, improves glucose tolerance, and reduces hyperinsulinemia during an oral glucose tolerance test (OGTT) and improves insulin secretory responsiveness ex vivo.
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