Clopamide

Modify Date: 2024-01-02 08:43:00

Clopamide Structure
Clopamide structure
Common Name Clopamide
CAS Number 636-54-4 Molecular Weight 345.845
Density 1.4±0.1 g/cm3 Boiling Point N/A
Molecular Formula C14H20ClN3O3S Melting Point 244-246ºC
MSDS N/A Flash Point N/A
Symbol GHS08
GHS08
Signal Word Danger

 Use of Clopamide


Clopamide is an orally active thiazide-like diuretic agent that inhibits the sodium-coupled chloride cotransporter SLC12A3. Clopamide has the potential for hypertension and cardiac failure research[1][2].

 Names

Name Clopamide
Synonym More Synonyms

 Clopamide Biological Activity

Description Clopamide is an orally active thiazide-like diuretic agent that inhibits the sodium-coupled chloride cotransporter SLC12A3. Clopamide has the potential for hypertension and cardiac failure research[1][2].
Related Catalog
In Vitro Clopamide is actively secreted by renal tubular cells and the True Tubular Excretion Fraction (TTEF) value is 10%[3].
In Vivo The venoconstrictor response to bradykinin is attenuated after oral administration of Clopamide (0.5 mg/kg), and by concomitant local infusion of cyclosporine-A (1-10 μg/min) in conscious dogs[4].
References

[1]. J J McNeil, et al. Clopamide: plasma concentrations and diuretic effect in humans. Clin Pharmacol Ther. 1987 Sep;42(3):299-304.

[2]. Yoshiteru Noutoshi, et al. Diuretics prime plant immunity in Arabidopsis thaliana. PLoS One. 2012;7(10):e48443.

[3]. B Odlind, et al. Renal tubular secretion and effects of chlorothiazide, hydrochlorothiazide and clopamide: a study in the avian kidney. Acta Pharmacol Toxicol (Copenh). 1982 Sep;51(3):187-97.

[4]. E Müller-Schweinitzer, et al. Interaction of cyclosporine-A with the renin-angiotensin system in canine veins. Naunyn Schmiedebergs Arch Pharmacol. 1989 Aug;340(2):252-7.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Melting Point 244-246ºC
Molecular Formula C14H20ClN3O3S
Molecular Weight 345.845
Exact Mass 345.091400
PSA 100.88000
LogP 1.59
Index of Refraction 1.613
Storage condition 2-8°C

 Safety Information

Symbol GHS08
GHS08
Signal Word Danger
Hazard Statements H317-H334
Precautionary Statements P261-P280-P284-P304 + P340-P342 + P311
Hazard Codes Xn
Risk Phrases R42/43
Safety Phrases 36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2935009090

 Customs

HS Code 2935009090
Summary 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

 Articles3

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Ultra high performance supercritical fluid chromatography coupled with tandem mass spectrometry for screening of doping agents. II: Analysis of biological samples.

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The potential and applicability of UHPSFC-MS/MS for anti-doping screening in urine samples were tested for the first time. For this purpose, a group of 110 doping agents with diverse physicochemical p...

Effects of pindolol, or a pindolol/clopamide combination preparation, on plasma lipid levels in essential hypertension. Hunter Hypertension Research Group.

Med. J. Aust. 150(11) , 646, 648, 651-2, (1989)

In an open study that was conducted in general practice, 22 patients with previously-untreated mild hypertension received an average daily dose of 11.7 mg of pindolol over a 50-week study period. The ...

 Synonyms

EINECS 211-261-7
Brinaldix
DT-327
4-Chloro-N-[(2R,6S)-2,6-dimethyl-1-piperidinyl]-3-sulfamoylbenzamide
Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,6-dimethyl-1-piperidinyl)-, cis-
CLOPAMIDUM
ChlosudiMepriMyl
Adurix
MFCD00941495
4-Chloro-N-(2,6-dimethylpiperidino)-3-sulfamoylbenzamide
3-(aminosulfonyl)-4-chloro-N-(2,6-dimethylpiperidin-1-yl)benzamide
Aquex
4-Chloro-N-(2,6-dimethylpiperidin-1-yl)-3-sulfamoylbenzamide
Benzamide, 3-(aminosulfonyl)-4-chloro-N-[(2R,6S)-2,6-dimethyl-1-piperidinyl]-
Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,6-dimethyl-1-piperidinyl)-
4-Chloro-N-(2,6-dimethyl-1-piperidinyl)-3-sulfamoylbenzamide