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Fosfenopril

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Catalog No. T20518Cas No. 95399-71-6
Alias SQ27519, SQ 27519, Fosinoprilic acid, Fosinoprilat

Fosfenopril (Fosinoprilat) is a potent angiotensin-converting enzyme (ACE) inhibitor that mitigates lipopolysaccharide-induced inflammation in monocytes through the suppression of TLR4/NF-κB signaling pathways, and Fosfenopril is utilized in cardiovascular and anti-inflammatory research to investigate molecular mechanisms of ACE inhibition.

Fosfenopril

Fosfenopril

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Purity: 99.05%
Catalog No. T20518Alias SQ27519, SQ 27519, Fosinoprilic acid, FosinoprilatCas No. 95399-71-6
Fosfenopril (Fosinoprilat) is a potent angiotensin-converting enzyme (ACE) inhibitor that mitigates lipopolysaccharide-induced inflammation in monocytes through the suppression of TLR4/NF-κB signaling pathways, and Fosfenopril is utilized in cardiovascular and anti-inflammatory research to investigate molecular mechanisms of ACE inhibition.
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1 mg$90-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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.
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Purity:99.05%
Color:White
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Product Introduction

Bioactivity
Description
Fosfenopril (Fosinoprilat) is a potent angiotensin-converting enzyme (ACE) inhibitor that mitigates lipopolysaccharide-induced inflammation in monocytes through the suppression of TLR4/NF-κB signaling pathways, and Fosfenopril is utilized in cardiovascular and anti-inflammatory research to investigate molecular mechanisms of ACE inhibition.
In vitro
Fosfenopril (0-10 μM) treatment for 5 minutes can inhibit the LPS-induced increase in TLR4 expression [1].
Fosfenopril (0-10 μM) treatment for 1 hour can reduce the LPS-activated NF-κB expression level [1].
Fosfenopril also inhibits the expression of LPS-induced pro-inflammatory cytokines (IL-6, IL-1β, and TNF-α) [1].
In vivo
Single intravenous injection of Fosfenopril (0.5 mg/kg bolus plus 0.1 mg/kg/min) can increase para-aminohippuric acid (PAH) clearance and glomerular filtration rate (GFR) in canines [3].
SynonymsSQ27519, SQ 27519, Fosinoprilic acid, Fosinoprilat
Chemical Properties
Molecular Weight435.49
FormulaC23H34NO5P
Cas No.95399-71-6
SmilesC(CP(CCCCC1=CC=CC=C1)(=O)O)(=O)N2C[C@@H](C[C@H]2C(O)=O)C3CCCCC3
Relative Density.1.238g/cm3
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (183.7 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 3.3 mg/mL (7.58 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2963 mL11.4813 mL22.9626 mL114.8132 mL
5 mM0.4593 mL2.2963 mL4.5925 mL22.9626 mL
10 mM0.2296 mL1.1481 mL2.2963 mL11.4813 mL
20 mM0.1148 mL0.5741 mL1.1481 mL5.7407 mL
50 mM0.0459 mL0.2296 mL0.4593 mL2.2963 mL
100 mM0.0230 mL0.1148 mL0.2296 mL1.1481 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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