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Pemirolast potassium

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Catalog No. T1425Cas No. 100299-08-9
Alias TWT-8152, BMY 26517

Pemirolast Potassium is the potassium salt form of pemirolast, a pyrimidinone derivative with antiallergic property. Pemirolast potassium (TWT-8152) exerts its action by blocking the antigen-mediated calcium ion influx into mast cells.

Pemirolast potassium

Pemirolast potassium

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Purity: 99.63%
Catalog No. T1425Alias TWT-8152, BMY 26517Cas No. 100299-08-9
Pemirolast Potassium is the potassium salt form of pemirolast, a pyrimidinone derivative with antiallergic property. Pemirolast potassium (TWT-8152) exerts its action by blocking the antigen-mediated calcium ion influx into mast cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$30In StockIn Stock
10 mg$48In StockIn Stock
25 mg$68In StockIn Stock
50 mg$85In StockIn Stock
100 mg$126In StockIn Stock
200 mg$163-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.63%
Appearance:solid
Color:White to Yellow
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Product Introduction

Pemirolast potassium AI Summary
Pemirolast potassium demonstrates antiviral activity, notably inhibiting the entry of the Ebola virus with significant potency, evidenced by AC50 values of 1.259 µM and 1258.9 nM in different assays. It also exhibits antiviral properties against SARS-CoV-2, albeit with varying efficacy. In Vero E6 cells, it showed a low inhibition index of 0.2426 for SARS-CoV-2 strain BavPat1. For SARS-CoV-2-induced cytotoxicity, it displayed 6.36% inhibition in Caco-2 cells at a 10 µM concentration over 48 hours and a 7.072% inhibition of the SARS-CoV-2 3CL-Pro protease at 20 µM. However, in Vero-6 cells, the inhibition rate was -0.09% at a 10 µM concentration after 48 hours, indicating limited efficacy. Additionally, Pemirolast potassium shows weak bioactivity in inhibiting human BSEP, MRP2, MRP3, and MRP4 activities, with IC50 values exceeding 133,000.0 nM in these assays, suggesting low potency in these transport processes..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Pemirolast Potassium is the potassium salt form of pemirolast, a pyrimidinone derivative with antiallergic property. Pemirolast potassium (TWT-8152) exerts its action by blocking the antigen-mediated calcium ion influx into mast cells.
In vitro
Pemirolast potassium inhibits the release of peptides from sensory nerves (substance P, neurokinin (NK) A, and CGRP) and inhibits the release of chemical mediators from tissue mast cells, which are commonly used in the treatment of allergic reactions.
In vivo
Pemirolast potassium inhibits the release of peptides from sensory nerves (substance P, neurokinin (NK) A, and CGRP) and inhibits the release of chemical mediators from tissue mast cells, which are commonly used in the treatment of allergic reactions.
SynonymsTWT-8152, BMY 26517
Chemical Properties
Molecular Weight266.31
FormulaC10H7KN6O
Cas No.100299-08-9
Smiles[K+].Cc1cccn2c1ncc(c2=O)c1[n-]nnn1
Relative Density.no data available
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
H2O: 10 mM, Sonication is recommended.
DMSO: Insoluble
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM3.7550 mL18.7751 mL37.5502 mL187.7511 mL
5 mM0.7510 mL3.7550 mL7.5100 mL37.5502 mL
10 mM0.3755 mL1.8775 mL3.7550 mL18.7751 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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