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Fluanisone

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Catalog No. T4275Cas No. 1480-19-9
Alias Sedalande, Haloanison

Fluanisone (Haloanison) is a butyrophenone derivative with sedative properties. It is a typical antipsychotic and is used in the treatment of schizophrenia.

Fluanisone

Fluanisone

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Purity: 99.94%
Catalog No. T4275Alias Sedalande, HaloanisonCas No. 1480-19-9
Fluanisone (Haloanison) is a butyrophenone derivative with sedative properties. It is a typical antipsychotic and is used in the treatment of schizophrenia.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$30In StockIn Stock
50 mg$55In StockIn Stock
100 mg$98In StockIn Stock
500 mg$238In StockIn Stock
1 mL x 10 mM (in DMSO)$30In StockIn 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:99.94%
Appearance:Solid
Color:White
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Product Introduction

Fluanisone AI Summary
Fluanisone demonstrates a wide range of bioactivities, including high affinity binding to multiple receptors and various pharmacological effects. It exhibits a high potency in displacing ligands from both the Dopamine receptor D2 (Ki = 2.9 nM) and the alpha-1 adrenergic receptor (Ki = 0.87 nM). It also shows moderate activity at the 5-hydroxytryptamine 2 receptor (Ki = 52.0 nM). The compound effectively suppresses conditioned avoidance behavior in rats and antagonizes apomorphine-induced climbing behavior in mice, with route-dependent efficacy (ED50 = 25.0 mg/kg orally and 0.4 mg/kg intraperitoneally). Additionally, it induces catalepsy in rats with an ED50 of 22.0 mg/kg intraperitoneally and modulates contractile activity and muscle tone in mice. Fluanisone also displays inhibitory activities against various enzymes and assays, including ALDH1A1, DNA Polymerase Beta, and 15-hLO-2, with varying potencies. Moreover, it possesses antiviral properties, inhibiting SARS-CoV-2 induced cytotoxicity in VERO-6 cells with an IC50 greater than 20,000 nM. The compound's pharmacokinetic properties are influenced by its logP (3.6) and logD7.4 (2.93) values, suggesting significant interactions with lipid environments..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Fluanisone (Haloanison) is a butyrophenone derivative with sedative properties. It is a typical antipsychotic and is used in the treatment of schizophrenia.
SynonymsSedalande, Haloanison
Chemical Properties
Molecular Weight356.43
FormulaC21H25FN2O2
Cas No.1480-19-9
SmilesCOC1=CC=CC=C1N1CCN(CCCC(=O)C2=CC=C(F)C=C2)CC1
Relative Density.1.146g/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: 50 mg/mL (140.28 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 2.5 mg/mL (7.01 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 mM2.8056 mL14.0280 mL28.0560 mL140.2800 mL
5 mM0.5611 mL2.8056 mL5.6112 mL28.0560 mL
10 mM0.2806 mL1.4028 mL2.8056 mL14.0280 mL
20 mM0.1403 mL0.7014 mL1.4028 mL7.0140 mL
50 mM0.0561 mL0.2806 mL0.5611 mL2.8056 mL
100 mM0.0281 mL0.1403 mL0.2806 mL1.4028 mL

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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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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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