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Delapril hydrochloride

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Catalog No. T3281Cas No. 83435-67-0
Alias indalapril, Delapril Hydrochloride, CV 3317, Alindapril Hydrochloride

Delapril hydrochloride (indalapril) is a prodrug; it is converted into two active metabolites, 5-hydroxy delapril diacid and delapril diacid. These metabolites bind completely to and inhibit angiotensin-converting enzyme (ACE), hence blocking angiotensin I to angiotensin II conversion.

Delapril hydrochloride

Delapril hydrochloride

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Purity: 97.45%
Catalog No. T3281Alias indalapril, Delapril Hydrochloride, CV 3317, Alindapril HydrochlorideCas No. 83435-67-0
Delapril hydrochloride (indalapril) is a prodrug; it is converted into two active metabolites, 5-hydroxy delapril diacid and delapril diacid. These metabolites bind completely to and inhibit angiotensin-converting enzyme (ACE), hence blocking angiotensin I to angiotensin II conversion.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$31In StockIn Stock
10 mg$56In StockIn Stock
25 mg$113In StockIn Stock
50 mg$147In StockIn Stock
100 mg$197In StockIn Stock
1 mL x 10 mM (in DMSO)$35In 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:97.45%
Appearance:Solid
Color:White
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Product Introduction

Delapril hydrochloride AI Summary
Delapril hydrochloride demonstrates bioactivity as an inhibitor in various assays, including blocking the entry of Ebola virus into cells and inhibiting human tyrosyl-DNA phosphodiesterase 1 (TDP1). It shows potency at varying concentrations in these assays, indicating potential antiviral and enzymatic inhibitory properties. However, it exhibits a low inhibition index (0.1107) in assays conducted on Vero E6 cells infected with SARS-CoV-2, showing minimal inhibition of cell viability compared to the control arbidol. Additionally, it inhibited SARS-CoV-2 induced cytotoxicity of Caco-2 cells by 26.34% at a concentration of 10 μM after 48 hours, as determined by high content imaging. Furthermore, Delapril hydrochloride has a 7.146% inhibition rate on SARS-CoV-2 3CL-Pro protease at a concentration of 20 µM, suggesting some potential bioactivity against this enzyme. However, in Vero-6 cells, it demonstrated a mere 0.03% inhibition rate at 10 μM concentration after 48 hours of exposure to the virus..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Delapril hydrochloride (indalapril) is a prodrug; it is converted into two active metabolites, 5-hydroxy delapril diacid and delapril diacid. These metabolites bind completely to and inhibit angiotensin-converting enzyme (ACE), hence blocking angiotensin I to angiotensin II conversion.
Synonymsindalapril, Delapril Hydrochloride, CV 3317, Alindapril Hydrochloride
Chemical Properties
Molecular Weight489.01
FormulaC26H33ClN2O5
Cas No.83435-67-0
SmilesCl.CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N(CC(O)=O)C1Cc2ccccc2C1
Relative Density.no data available
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 89 mg/mL (182 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (6.75 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 mM2.0449 mL10.2247 mL20.4495 mL102.2474 mL
5 mM0.4090 mL2.0449 mL4.0899 mL20.4495 mL
10 mM0.2045 mL1.0225 mL2.0449 mL10.2247 mL
20 mM0.1022 mL0.5112 mL1.0225 mL5.1124 mL
50 mM0.0409 mL0.2045 mL0.4090 mL2.0449 mL
100 mM0.0204 mL0.1022 mL0.2045 mL1.0225 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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