Canrenoate potassium

(Synonyms: 坎利酸钾; Aldadiene potassium; SC-14266)
目录号: PL07289 纯度: ≥99%
Canrenoate potassium 是一种释放 canrenone 的前药,也是一种有效的竞争性盐皮质激素受体 (mineralocorticoid receptor) 拮抗剂。Canrenoate potassium 作为一种利尿剂,用于高血压的研究。
CAS No. :2181-04-6
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中文名称
Canrenoate potassium
中文别名
坎利酸钾;刊利酸钾;17-羟基-3-氧孕烷4,6-二烯-21-羧酸
英文名称
Canrenoate potassium
英文别名
Potassium canrenoate;17-Hydroxy-3-oxopregna-4,6-diene-21-carboxylic acid potassium salt;Canrenoic acid potassium salt;CANRENOIC ACID POTASSIUM;17-Hydroxy-3-oxopregna-4,6-diene-21-carboxylic acid,Potassium canrenoate;Canrenoate potassium
Cas No.
2181-04-6
分子式
C22H29O4-.K+
分子量
396.56
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
详情描述
Canrenoate potassium 是一种释放 canrenone 的前药,也是一种有效的竞争性盐皮质激素受体 (mineralocorticoid receptor) 拮抗剂。Canrenoate potassium 作为一种利尿剂,用于高血压的研究。
产品详情
Canrenoate potassium 是一种释放 canrenone 的前药,也是一种有效的竞争性盐皮质激素受体 (mineralocorticoid receptor) 拮抗剂。Canrenoate potassium 作为一种利尿剂,用于高血压的研究。
生物活性
Canrenoate (Aldadiene) potassium, a prodrug that releases canrenone, is a potent, competitive mineralocorticoid receptor (aldosterone receptor) antagonist. Potassium canrenoate, as a diuretic, is used for the research of hypertension.
性状
Solid
体内研究(In Vivo)
Potassium canrenoate has been shown to cause in rats a dose-dependent increase in myelogenous leukemia and statistically significant increases in malignant tumor of the liver, thyroid, brain and mammary gland.
Potassium canrenoate (20 mg/kg/day; drinking water) reduces isoprenaline-induced cardiac fibrosis in the rat. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
ClinicalTrial
参考文献
[1]. Iqbal J, Andrew R, et al. Displacement of cortisol from human heart by acute administration of a mineralocorticoid receptor antagonist. J Clin Endocrinol Metab. 2014;99(3):915-922.
溶解度数据
In Vitro: H2O : 100 mg/mL (252.17 mM; ultrasonic and warming and heat to 60°C)配制储备液
搜索质检报告(COA)
[1]. Iqbal J, Andrew R, et al. Displacement of cortisol from human heart by acute administration of a mineralocorticoid receptor antagonist. J Clin Endocrinol Metab. 2014;99(3):915-922.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2