VU0071063
货号：
21897-1mg 基本售价：
350.0 元 规格：
1 mg
产品信息
概述| 货号 | 21897-1mg |
| 描述 | VU0071063 is a potent and selective activator of the inward-rectifier potassium channel (Kir) 6.2 and sulfonylurea receptor (SUR) 1 (EC50 = 7 µM using whole cell patch clamp electrophysiology).1 It is selective for SUR1-containing Kir6.1 or Kir6.2 channels over SUR2A, Kir2.1, Kir2.2, Kir2.3, Kir3.1/3/2, and voltage-gated potassium channel 2.1. VU0071063 inhibits glucose-stimulated calcium entry in isolated mouse pancreatic β-cells. |
性能| 供应商 | Cayman |
| 应用文献 |
1.Raphemot, R.,Swale, D.R.,Dadi, P.K., et al. Direct activation of β-cell KATP channels with a novel xanthine derivative. Mol. Pharmacol. 85(6), 858-865 (2014).
|
| 运输条件 | Room temperature in continental US; may vary elsewhere |
| 存放说明 | -20 |
| 纯度 | ≥98% |
| 计算分子量 | 326.4 |
| 分子式 | C18H22N4O2 |
| CAS号 | 333415-38-6 |
| 稳定性 | ≥ 2 years |
声明| 本官网所有报价均为常温或者蓝冰运输价格，如有产品需要干冰运输，需另外加收干冰运输费。 |
