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Revaprazan hydrochloride

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Catalog No. T2405Cas No. 178307-42-1
Alias YH1885

Revaprazan hydrochloride (YH1885) is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.

Revaprazan hydrochloride

Revaprazan hydrochloride

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Purity: 99.91%
Catalog No. T2405Alias YH1885Cas No. 178307-42-1
Revaprazan hydrochloride (YH1885) is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$37In StockIn Stock
25 mg$74In StockIn Stock
50 mg$115In StockIn Stock
100 mg$181In StockIn Stock
500 mg$448In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.91%
Color:White
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Product Introduction

Revaprazan hydrochloride AI Summary
Revaprazan hydrochloride inhibits the H^+/K^+/ATPase enzyme, with an IC50 value of 350.0 nM. It has a logP(lung) value of 1.34, indicating its affinity or distribution within lung tissues compared to plasma in rats. Additionally, Revaprazan hydrochloride exhibits antiviral activity; it inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 cells with a high inhibition rate of 90.92% at a concentration of 10 μM after 48 hours. In VERO-6 cells, the compound shows 5.47% inhibition of SARS-CoV-2 induced cytotoxicity under similar conditions. Furthermore, it inhibits the SARS-CoV-2 3CL-Pro protease by 18.63% at a concentration of 20 μM through a FRET response from a peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Revaprazan hydrochloride (YH1885) is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.
SynonymsYH1885
Chemical Properties
Molecular Weight398.9
FormulaC22H24ClFN4
Cas No.178307-42-1
SmilesCl.CC1N(CCc2ccccc12)c1nc(Nc2ccc(F)cc2)nc(C)c1C
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
DMSO: 3.99 mg/mL (10 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.51 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 mM2.5069 mL12.5345 mL25.0689 mL125.3447 mL
5 mM0.5014 mL2.5069 mL5.0138 mL25.0689 mL
10 mM0.2507 mL1.2534 mL2.5069 mL12.5345 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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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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