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Apilimod

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Catalog No. T2018Cas No. 541550-19-0
Alias STA 5326

Apilimod (STA 5326) inhibits the production of IL-12 and IL-23 and reduces dendritic cell infiltration in psoriasis.

Apilimod

Apilimod

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🥰Excellent
Purity: 99.89%
Catalog No. T2018Alias STA 5326Cas No. 541550-19-0
Apilimod (STA 5326) inhibits the production of IL-12 and IL-23 and reduces dendritic cell infiltration in psoriasis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$43In StockIn Stock
10 mg$68In StockIn Stock
25 mg$81In StockIn Stock
50 mg$97In StockIn Stock
100 mg$158In StockIn Stock
1 mL x 10 mM (in DMSO)$48In 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:99.89%
Color:White
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Product Introduction

Apilimod AI Summary
Apilimod exhibits potent antiviral activity against SARS-CoV-2, with an EC50 value of 23.0 nM in a high-content imaging assay using Vero E6 cells infected with the USA-WA1/2020 isolate after 24 hours. Additionally, its ability to inhibit SARS-CoV-2 induced cytotoxicity has been demonstrated in multiple cell lines, including Caco-2 cells, where it showed an inhibition rate of 8.48% at 10 µM after 48 hours, and in Vero E6 cells, where it exhibited an inhibition rate of 5.69% at 10 µM after 48 hours. The compound also inhibits the SARS-CoV-2 3CL-Pro protease with an inhibition rate of 10.54% at 20 µM. Further assays indicate inhibition of viral growth with an IC50 of less than 80 nM in Vero E6 cells and 7 nM in A549-ACE2 cells. In addition to its antiviral properties, Apilimod inhibits human PIKFYVE with IC50 values ranging from 0.309 nM to 15.0 nM, and demonstrates HDAC6 inhibition with modest rates of 1.14% to 4.44%. It also shows significant binding affinity to human wild type partial length PIKFYVE with a dissociation constant of 0.075 nM. However, it exhibits cytotoxicity against Vero E6 cells at concentrations above 1000 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Apilimod (STA 5326) inhibits the production of IL-12 and IL-23 and reduces dendritic cell infiltration in psoriasis.
Targets&IC50
PIKfyve:14 nM
SynonymsSTA 5326
Chemical Properties
Molecular Weight418.49
FormulaC23H26N6O2
Cas No.541550-19-0
SmilesCc1cccc(\C=N\Nc2cc(nc(OCCc3ccccn3)n2)N2CCOCC2)c1
Relative Density.1.24
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: 200 mg/mL (477.91 mM), Sonication and heating are recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (11.95 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 mM2.3895 mL11.9477 mL23.8954 mL119.4772 mL
5 mM0.4779 mL2.3895 mL4.7791 mL23.8954 mL
10 mM0.2390 mL1.1948 mL2.3895 mL11.9477 mL
20 mM0.1195 mL0.5974 mL1.1948 mL5.9739 mL
50 mM0.0478 mL0.2390 mL0.4779 mL2.3895 mL
100 mM0.0239 mL0.1195 mL0.2390 mL1.1948 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:
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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