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CAS: 2016-88-8
分子式: C6H8ClN7O·HCl
分子量: 266.11
中文名称: 
氨氯吡咪
阿米洛利
盐酸氨氯吡咪
脒吡嗪盐酸盐
盐酸阿米洛利
英文名称: 
Amiloride hydrochloride
Arumil
n-amidino-3,5-diamino-6-chloro-pyrazinecarboxamid monohydrochloride
amiloride chloride
amiprazidine
amiloride hydrochloride hydrate
性质描述: 黄色或绿黄色粉末。熔点293.5℃。溶于水,几乎无臭,氨氯吡咪碱[2609-46-3]熔点,240.5-241.5℃。
用途: 为弱效利尿药。作用与氨苯蝶相似,为目前排钠甾钾利尿药中作用最强的药物。
推荐供应商
货号品牌产品名称规格包装、参考价格
129876Sigma-AldrichAmiloride, Hydrochloride-CAS 2016-88-8-CalbiochemAn inhibitor of angiogenesis.1107.04元/100 MG;   咨询

产品说明

一般描述

An inhibitor of angiogenesis. Inhibits capillary morphogenesis completely and reversibly at approximately 130 µM. At low concentrations, acts as a potent and specific inhibitor of transmembrane Na+ entry and Na+,K+-ATPase. Also acts as an inhibitor of urokinase-type plasminogen activator (uPA). Blocks smooth muscle responses to contractile stimuli and palytoxin-induced conductance in skeletal muscle. Reduces electrical potential across tubular epithelium. At higher concentrations, blocks the Na+/H+ exchange pathway.
An inhibitor of angiogenesis. At low concentrations, acts as a potent and specific inhibitor of transmembrane Na+ entry and Na+/H+ ATPase. Inhibits smooth muscle responses to contractile stimuli. Blocks palytoxin-induced conductance in skeletal muscle. Reduces the electrical potential across tubular epithelium. At higher concentrations, blocks the Na+/H+ exchange pathway.

包装

100 mg in Alu drum

生化/生理作用

Primary Target
capillary morphogenesis
Product does not compete with ATP.
Cell permeable: no
Reversible: yes
Target IC50: 130 µM inhibiting capillary morphogenesis completely and reversibly

警告

Toxicity: Toxic (F)

重悬

Following reconstitution, aliquot and freeze (-20°C). Aqueous stock solutions are stable for up to 6 months at -20°C.

其他说明

Knoll, A., et al. 1999. Microvasc. Res.58, 1.
Swiercz, R., et al. 1999. Oncol. Rep.6, 523.
Moran, A., et al. 1995. Am. J. Physiol. 268, C350.
Alliegro, M.C., et al. 1993. J. Exp. Zool. 267, 245.
Sugiyama, S., et al. 1988. J. Biol. Chem.263, 8215.
Yoshida, K., et al. 1988. Biochem. Biophys. Res. Commun.154, 101.
Sariban-Sotorabay, S., and Benos, D.J. 1986. Am. J. Physiol.250, C175.
Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C6H8ClN7O · xHCl
分子量229.63 (free base basis)
NACRESNA.77

产品性质

质量水平100
测定≥98% (HPLC)
形式solid
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
desiccated (hygroscopic)
protect from light
颜色 off-white to yellow
溶解性water: 2.5 mg/mL
DMSO: 5 mg/mL
运输ambient
储存温度10-30℃
InChI1S/C6H8ClN7O.ClH/c7-2-4(9)13-3(8)1(12-2)5(15)14-6(10)11;/h(H4,8,9,13)(H4,10,11,14,15);1H
InChI keyACHKKGDWZVCSNH-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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