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Merck
CN

H149

Supelco

氢氯噻嗪

别名:

6-氯-3,4-二氢-2H-1,2,4-苯并噻二嗪-7-磺酰胺1,1-二氧化物, 6-氯-7-磺酰胺-3,4-二氢-1,2,4-苯并噻二嗪-1,1-二氧化物

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关于此项目

经验公式(希尔记法):
C7H8ClN3O4S2
化学文摘社编号:
分子量:
297.74
EC 号:
MDL编号:
UNSPSC代码:
41116107
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SMILES字符串

NS(=O)(=O)c1cc2c(NCNS2(=O)=O)cc1Cl

InChI

1S/C7H8ClN3O4S2/c8-4-1-5-7(2-6(4)16(9,12)13)17(14,15)11-3-10-5/h1-2,10-11H,3H2,(H2,9,12,13)

InChI key

JZUFKLXOESDKRF-UHFFFAOYSA-N

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一般描述

Hydrochlorothiazide is a type of thiazide diuretics used as a hypertensive agent.

应用

Hydrochlorothiazide may be used as a reference standard in the determination of hydrochlorothiazide in pharmaceutical formulations using first-derivative ultraviolet spectrophotometry and high-performance liquid chromatography (HPLC).

生化/生理作用

碳酸酐酶抑制剂

象形图

Health hazard

警示用语:

Warning

危险声明

危险分类

Carc. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Simultaneous determination of valsartan and hydrochlorothiazide in tablets by first-derivative ultraviolet spectrophotometry and LC.
Satana E, et al.
Journal of Pharmaceutical and Biomedical Analysis, 25(5-6), 1009-1013 (2001)
Ahmed H Ahmed et al.
Journal of medicinal chemistry, 53(5), 2197-2203 (2010-02-19)
Glutamate receptors are the most prevalent excitatory neurotransmitter receptors in the vertebrate central nervous system and are important potential drug targets for cognitive enhancement and the treatment of schizophrenia. Allosteric modulators of AMPA receptors promote dimerization by binding to a
Barry L Carter et al.
Hypertension (Dallas, Tex. : 1979), 43(1), 4-9 (2003-11-26)
Thiazide diuretics are one of the preferred pharmacologic treatments for hypertension. Hydrochlorothiazide and chlorthalidone have been the 2 most commonly used diuretics in major clinical trials. Treatment guidelines and compendia often consider these 2 drugs interchangeable agents within the class
Loretta Aureli et al.
Journal of medicinal chemistry, 48(7), 2469-2479 (2005-04-02)
A novel class of 2-(R)-phenylpropionamides has been recently reported to inhibit in vitro and in vivo interleukin-8 (CXCL8)-induced biological activities. These CXCL8 inhibitors are derivatives of phenylpropionic nonsteroidal antiinflammatory drugs (NSAIDs), high-affinity ligands for site II of human serum albumin
Pil H Lee et al.
Bioorganic & medicinal chemistry letters, 20(1), 69-73 (2009-12-08)
A multiple linear regression QSAR model was developed based on a set of 61 compounds with internally consistent permeability data measured across Franz cell. The data was normalized using a mean permeability value of a reference compound, 3-isobutyl-1-methylxanthine (IBMX). The

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