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Azosemide
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Azosemide图片
规格:98%
分子量:370.84
包装与价格:
包装价格(元)
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
Azosemide 是一种磺胺类环利尿剂,一种有效的 NKCC1 抑制剂,对 hNKCC1A 和 NKCC1B 的 IC50 分别为 0.246 µM 和 0.197 µM。
货号:ajcx15262
CAS:27589-33-9
分子式:C12H11ClN6O2S2
分子量:370.84
溶解度:DMSO: 250 mg/mL (674.15 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Azosemide, a sulfonamide loop diuretic, is a potent NKCC1 inhibitor with IC50s of 0.246 µM and 0.197 µM for hNKCC1A and NKCC1B, respectively[1].

Azosemide inhibits the sodium-potassium-chloride-cotransporter human variants hNKCC1A and hNKCC1B[1].

Azosemide shows a smaller AUC (81.9% decrease), shorter terminal half-life (50.9% decrease) and MRT (64.1% decrease), faster CL (454% increase), CLR (853% increase) and CLNR (307% increase) for NARs[2]. Animal Model: Male Sprague-Dawley rats (control rats, weighing 310345 g) and NARs (weighing 220315 g) of 9 weeks of age[2]

[1]. Hampel P, et al. Azosemide is more potent than bumetanide and various other loop diuretics to inhibit the sodium-potassium-chloride-cotransporter human variants hNKCC1A and hNKCC1B. Sci Rep. 2018 Jun 29;8(1):9877. [2]. Kim EJ, et al. Pharmacokinetics and pharmacodynamics of intravenous azosemide in mutant Nagaseanalbuminemic rats. Drug Metab Dispos. 2003 Feb;31(2):194-201.