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Fipamezole (Synonyms: JP-1730, JP1730, JP 1730, BVF-025)

Catalog No. T24064 Copy Product Info
Purity: 99.97%
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Fipamezole is a potent alpha2 adrenergic receptor antagonist that may be useful for studying autonomic dysfunction in Parkinson's disease.

Fipamezole

Copy Product Info
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Catalog No. T24064
Synonyms JP-1730, JP1730, JP 1730, BVF-025

Fipamezole is a potent alpha2 adrenergic receptor antagonist that may be useful for studying autonomic dysfunction in Parkinson's disease.

Fipamezole
Cas No. 150586-58-6
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$377In StockIn Stock
5 mg$810In StockIn Stock
10 mg$913In StockIn Stock
25 mg$1,060In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.97%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Fipamezole AI Summary
Fipamezole demonstrates significant antihypothermic activity in NMRI mice when administered either orally (po) or intraperitoneally (ip), effectively inhibiting guanabenz-induced hypothermia. It has an ED50 of 1.87 mg/kg for oral administration and 0.47 mg/kg for intraperitoneal administration. This compound displaces [3H]-RX821002 from adrenergic alpha2B and alpha-2C receptors with Ki values of 6.761 nM and 13.8 nM, respectively, and acts as an antagonist at the adrenergic alpha2A receptor with a pKb value of 7.84. Additionally, Fipamezole displaces [3H]-prazosin from the adrenergic alpha-1b receptor with a Ki value of 2089.3 nM. At a dose of 10 mg/kg intraperitoneally, it increases normetanephrine levels in the mouse cortex by 247.0% following microwave irradiation..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Fipamezole is a potent alpha2 adrenergic receptor antagonist that may be useful for studying autonomic dysfunction in Parkinson's disease.
Targets&IC50
α2B-adrenoceptor (human):17 nM (Ki), α2C-adrenoceptor (human):55 nM (Ki), α2A-adrenoceptor (human):9.2 nM (Ki)
SynonymsJP-1730, JP1730, JP 1730, BVF-025
Chemical Properties
Molecular Weight230.28
FormulaC14H15FN2
Cas No.150586-58-6
SmilesC(C)C1(CC=2C(C1)=CC=C(F)C2)C3=CN=CN3
Relative Density.1.31g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 55 mg/mL (238.84 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.3425 mL21.7127 mL43.4254 mL217.1270 mL
5 mM0.8685 mL4.3425 mL8.6851 mL43.4254 mL
10 mM0.4343 mL2.1713 mL4.3425 mL21.7127 mL
20 mM0.2171 mL1.0856 mL2.1713 mL10.8563 mL
50 mM0.0869 mL0.4343 mL0.8685 mL4.3425 mL
100 mM0.0434 mL0.2171 mL0.4343 mL2.1713 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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