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Sufotidine

Sufotidine
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Purity:100%
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Sufotidine

Catalog No. T68146Cas No. 80343-63-1
Sufotidine (AH 25352X) is a highly selective competitive H2 receptor antagonist.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$250In Stock
5 mg$623In Stock
10 mg$887In Stock
25 mg$1,330In Stock
50 mg$1,780In Stock
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Product Introduction

Bioactivity
Description
Sufotidine (AH 25352X) is a highly selective competitive H2 receptor antagonist.
In vitro
The acid inhibitory effect of sufotidine, a potent, long-lasting, competitive H2-receptor antagonist, was studied in 12 healthy males in a double-blind, randomized, three-way cross-over study of the effect of placebo, sufotidine 600 mg nocte and sufotidine 600 mg b.d. given over 15 days. On days 1 and 15 of dosing with each regimen, each subject's 24-hour ambulatory intragastric acidity was measured by radiotelemetry, and 24-hour plasma gastrin profiles were derived from hourly venous blood samples. Acid suppression was calculated as the decrease in the area under the curve of hydrogen ion activity vs time from that observed on placebo, and 24-h plasma gastrin was calculated as the area under the curve of plasma gastrin concentration vs time. 24h intragastric acidity during the fifteenth day of dosing with sufotidine 600 mg nocte and sufotidine 600 mg b.d. did not differ significantly, but on the first and fifteenth day of dosing nocturnal acidity was decreased to a greater extent by sufotidine 600 mg nocte than sufotidine 600 mg b.d. (P less than 0.005). After 15 days, the acid suppression afforded by sufotidine 600 mg b.d. was significantly attenuated (P less than 0.0005); this was associated with a rise in 24-h plasma gastrin (P less than 0.001). Thus, tolerance to the acid-inhibitory effect of H2-receptor antagonists exists and is of rapid onset.[1]
AliasAH 25352X, AH25352X, AH-25352X
Chemical Properties
Molecular Weight421.56
FormulaC20H31N5O3S
Cas No.80343-63-1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 55 mg/mL (130.47 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3721 mL11.8607 mL23.7214 mL118.6071 mL
5 mM0.4744 mL2.3721 mL4.7443 mL23.7214 mL
10 mM0.2372 mL1.1861 mL2.3721 mL11.8607 mL
20 mM0.1186 mL0.5930 mL1.1861 mL5.9304 mL
50 mM0.0474 mL0.2372 mL0.4744 mL2.3721 mL
100 mM0.0237 mL0.1186 mL0.2372 mL1.1861 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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