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Cadralazine (Synonyms: ISF-2469, ISF2469, ISF 2469)

Catalog No. T26939 Copy Product Info
Purity: 99.65%
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Cadralazine (ISF 2469) is a peripheral arteriolar vasodilator and can be used in studies about acting as an antihypertensive drug.

Cadralazine

Copy Product Info
🥰Excellent
Catalog No. T26939
Synonyms ISF-2469, ISF2469, ISF 2469

Cadralazine (ISF 2469) is a peripheral arteriolar vasodilator and can be used in studies about acting as an antihypertensive drug.

Cadralazine
Cas No. 64241-34-5
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Pack SizePriceUSA StockGlobal StockQuantity
5 mg$39-In Stock
10 mg$64-In Stock
25 mg$133-In Stock
50 mg$215-In Stock
100 mg$305-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.65%
Appearance:Solid
Color:White
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Product Introduction

Cadralazine AI Summary
Cadralazine demonstrates bioactivity in blocking the entry of the Ebola virus, with an AC50 ranging from 2.818 µM to 3162.3 nM, indicating potential inhibitory effects on the virus's entry process. Additionally, the compound exhibits antiviral activity by inhibiting SARS-CoV-2-induced cytotoxicity in both Caco-2 and Vero-6 cells. Specifically, in Caco-2 cells, Cadralazine shows a 2.11% inhibition rate at a concentration of 10 µM after 48 hours. In Vero-6 cells, the compound exhibits a 0.05% inhibition rate under similar conditions. Further, Cadralazine inhibits the SARS-CoV-2 3CL-Pro protease at a concentration of 20 µM, although it shows an inhibition percentage of -6.669%. Additionally, the compound inhibits human HDAC6 enzyme activity, showing a decrease of 12.37% in a commercial peptide substrate assay and an increase of 2.11% in a custom peptide substrate assay. Beyond these activities, Cadralazine has demonstrated a wide range of binding affinities for various receptors and enzymes, such as human ADRB2, human OPRK1, human HTR2C, and more, with AC50 values typically exceeding 30000.0 nM. It has been evaluated for inhibition of enzymes like human PTGS2 (AC50 of 2500.0 nM) and human PDE4D (AC50 greater than 30000.0 nM). The compound also shows agonist and antagonist activities for receptors including human HRH2, human ADRA2A, human HTR1A, and human DRD1, with AC50 values generally greater than 30000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Cadralazine (ISF 2469) is a peripheral arteriolar vasodilator and can be used in studies about acting as an antihypertensive drug.
SynonymsISF-2469, ISF2469, ISF 2469
Chemical Properties
Molecular Weight283.33
FormulaC12H21N5O3
Cas No.64241-34-5
SmilesN(CC(C)O)(CC)C1=CC=C(NNC(OCC)=O)N=N1
Relative Density.1.1585 g/cm3 (Estimated)
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 (705.89 mM), Sonication and heating to 60℃ are recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (17.65 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 mM3.5295 mL17.6473 mL35.2945 mL176.4727 mL
5 mM0.7059 mL3.5295 mL7.0589 mL35.2945 mL
10 mM0.3529 mL1.7647 mL3.5295 mL17.6473 mL
20 mM0.1765 mL0.8824 mL1.7647 mL8.8236 mL
50 mM0.0706 mL0.3529 mL0.7059 mL3.5295 mL
100 mM0.0353 mL0.1765 mL0.3529 mL1.7647 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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

You can also refer to dose conversion for different animals. More Dose Conversion

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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