WNK463
规格
Cas Number | 2012607-27-9 |
规格或纯度 | ≥99% |
纯度 | ≥99% |
包装 | 100mg 或 50mg 或 10mg 或 5mg 或 25mg |
产品信息
品牌 | 阿拉丁 |
溶解性 | Solubility (25°C) In vitro DMSO: 92 mg/mL (198.5 mM); Ethanol: 92 mg/mL (198.5 mM); Water: Insoluble; |
简短描述 | 丝氨酸/苏氨酸激酶抑制剂 |
英文简短描述 | Serine/threonin kinase Inhibitors |
过滤标签 | Ser/Thr Protease,Metabolic Enzyme/Protease |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
生化和生理学机理 | WNK463 是一种泛 WNK 激酶抑制剂。它能有效抑制所有四种 WNK 家族成员(WNK1、WNK2、WNK3 和 WNK4)的体外激酶活性。 |
英文描述 |
Information WNK463 WNK463 is a pan-WNK-kinase inhibitor. It potently inhibits the in vitro kinase activity of all four WNK family members (WNK1, WNK2, WNK3, and WNK4). Targets WNK-kinase In vitro WNK463 potently inhibited the in vitro kinase activity of all four WNK family members (WNK1, WNK2, WNK3, and WNK4). WNK463 also inhibited WNK1-catalyzed phosphorylation of the native WNK substrate, oxidative stress response 1 (OSR1) in a biochemical assay and in human embryonic kidney 293 (HEK293) cells that express exogenous OSR1 and that are activated by sorbitol-mediated osmotic stress. In vivo In rodent models of hypertension, WNK463 affects blood pressure and body fluid and electrolyte homeostasis. WNK463 is orally bioavailable in C57BL/6 mice (100%) and Sprague Dawley rats (74%), with a half-life of 3.6 and 2.1 h, respectively. In spontaneously hypertensive rats (SHRs), WNK463 administered orally (p.o.) at 1, 3, or 10 mg per kg body weight (mg/kg) p.o. achieved maximum plasma concentration (Cmax) values of 88, 441, and 1,170 nM, respectively. These exposures produced dose-dependent decreases in blood pressure and simultaneous increases in heart rate in conscious SHRs. Moreover, WNK463 produced significant and dose-dependent increases in urine output as well as urinary sodium and potassium excretion rates. Orally administered WNK463 also significantly decreasedblood pressure in these hypertensive mice. WNK463 elicited in vivo cardiovascular and renal effects through WNK kinase inhibition. |