2. Metabolic Enzyme/Protease
  3. Carbonic Anhydrase
  4. Quinethazone

Quinethazone  (Synonyms: 喹乙宗； 喹噻酮； 喹乙唑酮)

目录号: HY-B1364
产品使用指南

摩尔计算器

Quinethazone 是一种具有口服活性的利尿剂，也是一种碳酸酐酶（carbonic anhydrase）的弱抑制剂，可用于高血压研究。

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Quinethazone Chemical Structure

Quinethazone Chemical Structure

CAS No. : 73-49-4

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规格 价格 是否有货
2500 μg ￥6880
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Customer Review

Other Forms of Quinethazone:

Quinethazone 相关抗体

Top Publications Citing Use of Products

查看 Carbonic Anhydrase 亚型特异性产品:

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CA CA I CA Ⅱ CA Ⅸ CA XII

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Quinethazone is an orally active diuretic agent and is also a weak inhibitor of carbonic anhydrase. Quinethazone can be used for hypertension research[1][2].

体内研究
(In Vivo)

Quinethazone (50 mg/kg; p.o.; daily for 2 weeks) lowers blood pressure of renal hypertensive rats in association with a decrease in potassium but no change in water or sodium contents of aorta wall[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Five- to 6-week-old Long Evans male rats, hypertension model[1]
Dosage: 50 mg/kg
Administration: Oral, daily for 2 weeks
Result: Had no significant effect on sodium or water distribution in arterial tissue of hypertensive rats, but decreased approximate 20% intra-cellular content of potassium
分子量

289.74

Formula

C10H12ClN3O3S
CAS 号
中文名称

喹乙宗； 喹噻酮； 喹乙唑酮
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

Quinethazone 相关分类

  • 摩尔计算器

  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Quinethazone73-49-4喹乙宗 喹噻酮 喹乙唑酮Carbonic AnhydraseCarbonate dehydratasehypertensiondiureticpotassiumInhibitorinhibitorinhibit

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