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Tetrahydrozoline

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Catalog No. T0397Cas No. 84-22-0
Alias Tetryzoline, Tetryzolin

Tetrahydrozoline (Tetryzoline), an alpha agonist, have an effect on the constriction of conjunctival blood vessels. This contributes to relieve the redness of the eye resulted from minor ocular irritants.

Tetrahydrozoline

Tetrahydrozoline

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Purity: 99.77%
Catalog No. T0397Alias Tetryzoline, TetryzolinCas No. 84-22-0
Tetrahydrozoline (Tetryzoline), an alpha agonist, have an effect on the constriction of conjunctival blood vessels. This contributes to relieve the redness of the eye resulted from minor ocular irritants.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$33In StockIn Stock
100 mg$48In StockIn Stock
500 mg$129-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:99.77%
Appearance:Solid
Color:White
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Product Introduction

Tetrahydrozoline AI Summary
Tetrahydrozoline exhibits a range of bioactivities across different biological systems. It demonstrates central hypotensive activity with a 25% decrease in arterial pressure in anesthetized normotensive rats and induces hypertensive activity with a 60 mmHg increase in pithed rats. The compound has a partition coefficient (LogD) of -0.9 in octanol/buffer at pH 7.4 and shows binding affinities to alpha-1 and alpha-2 adrenergic receptors, with IC50 values of 1600.0 nM and 30.0 nM, respectively. It also interacts with the alpha-adrenergic receptors in the rabbit jejunum and rat brain. Moreover, Tetrahydrozoline has shown various receptor and enzyme activities, including: - Potentiation of the human D1 dopamine receptor at 2592.8 nM. - Inhibition of mammalian selenoprotein thioredoxin reductase 1 at 14125.4 nM. - Inhibition of regulator of G protein signaling 4 at 29.9 nM. - Enhancement of Arylsulfatase A at 756.9 nM. In antiviral research, it inhibits SARS-CoV-2 induced cytotoxicity of VERO-6 cells with modest efficacy (IC50 > 19952.62 nM) and shows 17.25% inhibition against SARS-CoV-2 3CL-Pro protease at 20 µM. The compound also displayed varied inhibition rates against the human HDAC6 enzyme, suggesting inhibitory activity. The compound further displays binding affinities for human ADRA2A, HTR1A, OPRM1, and ADRA1A receptors, with notable agonist activity at human ADRA1A (AC50 of 6.1 nM). For other evaluated targets, significant activity was not observed (AC50 > 30000.0 nM). Tetrahydrozoline is noted for its absence of hepatic side effects according to the Drug Induced Liver Injury Prediction System (DILIps) training set, confirming a safe hepatic profile. Its basic pKa value is determined to be 10.6, indicating its behavior in biological environments. These diverse bioactivities highlight its significance for further pharmacological and antiviral studies..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Tetrahydrozoline (Tetryzoline), an alpha agonist, have an effect on the constriction of conjunctival blood vessels. This contributes to relieve the redness of the eye resulted from minor ocular irritants.
SynonymsTetryzoline, Tetryzolin
Chemical Properties
Molecular Weight200.28
FormulaC13H16N2
Cas No.84-22-0
SmilesC1CN=C(N1)C1CCCc2ccccc12
Relative Density.1.2 g/cm3
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: 45 mg/mL (224.69 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.99 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 mM4.9930 mL24.9650 mL49.9301 mL249.6505 mL
5 mM0.9986 mL4.9930 mL9.9860 mL49.9301 mL
10 mM0.4993 mL2.4965 mL4.9930 mL24.9650 mL
20 mM0.2497 mL1.2483 mL2.4965 mL12.4825 mL
50 mM0.0999 mL0.4993 mL0.9986 mL4.9930 mL
100 mM0.0499 mL0.2497 mL0.4993 mL2.4965 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:
% DMSO
%
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% Saline/PBS/ddH2O

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