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Alfuzosin

    
99.50%

Alfuzosin

源叶(MedMol)
S86589 一键复制产品信息
81403-80-7
C19H27N5O4
389.45
阿夫唑嗪;N[3-[(4-氨基-6,7-二甲氧基-2-喹唑啉基)甲基氨基]丙基]四氢-2-呋喃甲酰胺;阿夫唑嗪(N-[3-[(4-氨基-6,7-二甲氧基-2-喹唑啉基)甲基氨基丙基]四氢-2-呋喃甲酰胺);n-[3-[(4-amino-6,7-dimethoxy-quinazolin-2-yl)methylamino]propyl]tetrahydrofuran-2-carboxamide;ALF
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S86589-5mg买3赠1
99.50%

¥220.00

9 - - - -
S86589-25mg买3赠1
99.50%

¥710.00

9 - - - -
S86589-100mg买3赠1
99.50%

¥1800.00

7 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Alfuzosin (SL 77499-10) is an orally active, selective and competitive α1-adrenoceptor antagonist. Alfuzosin relaxes the muscles of the prostate and bladder neck, aiding in urination. Alfuzosin can be used in study of benign prostatic hyperplasia (BPH)
靶点: Adrenergic Receptor
体内研究: Alfuzosin hydrochloride (10 mg/kg, p.o.; single) potently antagonizes phenylephrine-induced increases in urethral and arterial pressures up to 6 hours post dosing. Animal Model: Male Wistar rats (250-450 g). Dosage: 10 mg/kg Administration: Oral administration; single. Result: Increased prostatic concentrations to 4.1-8.6 times higher than plasma concentration.
参考文献: 1. Martin DJ, et al. Relationship between the effects of alfuzosin on rat urethral and blood pressures and its tissue concentrations. Life Sci. 1998;63(3):169-76. 2. Wilde MI, et al. Alfuzosin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in benign prostatic hyperplasia. Drugs. 1993 Mar;45(3):410-29.
溶解性: Soluble  in  DMSO
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.568 ml 12.839 ml 25.677 ml
5 mM 0.514 ml 2.568 ml 5.135 ml
10 mM 0.257 ml 1.284 ml 2.568 ml
50 mM 0.051 ml 0.257 ml 0.514 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

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摩尔浓度计算器

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