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Oxyfedrine L-form HCl

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Catalog No. T24579Cas No. 16777-42-7
Alias Oxyfedrine L-form hydrochloride, Modacor, Ildamen, D-563, D563, D 563

Oxyfedrine L-form HCl (Ildamen) is a partial agonist at beta-adrenergic receptors and acts as a coronary vasodilator and cardiotonic agent.

Oxyfedrine L-form HCl

Oxyfedrine L-form HCl

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Purity: 99.57%
Catalog No. T24579Alias Oxyfedrine L-form hydrochloride, Modacor, Ildamen, D-563, D563, D 563Cas No. 16777-42-7
Oxyfedrine L-form HCl (Ildamen) is a partial agonist at beta-adrenergic receptors and acts as a coronary vasodilator and cardiotonic agent.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$88In StockIn Stock
5 mg$198In StockIn Stock
10 mg$347In StockIn Stock
25 mg$538In StockIn Stock
50 mg$778In StockIn Stock
100 mg$993In StockIn Stock
200 mg$1,330-In Stock
1 mL x 10 mM (in DMSO)$226In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.57%
Appearance:Solid
Color:White
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Product Introduction

Oxyfedrine L-form HCl AI Summary
Oxyfedrine L-form HCl exhibits a range of bioactivities, including the inhibition of human tyrosyl-DNA phosphodiesterase 1 (TDP1) with varying potencies, potential gametocytocidal properties, and the ability to block the entry of the Ebola virus. Notably, this compound also demonstrates significant antiviral activities against SARS-CoV-2. It shows a 6.41% inhibition of cytotoxicity in Caco-2 cells at a concentration of 10 μM after 48 hours. Additionally, Oxyfedrine L-form HCl inhibits the SARS-CoV-2 3CL-Pro protease with 91.57% inhibition at 20 μM and an IC50 of 2350.0 nM, though it is less effective against the MERS 3CL-Pro protease, with an inhibition percentage of 19.0% at 10 μM and an IC50 greater than 10000.0 nM. Moreover, the compound exhibits minimal inhibition of virus-induced cytotoxicity in VERO-6 cells, with an inhibition rate of 0.03% at 10 μM after 48 hours. Oxyfedrine L-form HCl shows potency in the nanomolar and micromolar ranges across various assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Oxyfedrine L-form HCl (Ildamen) is a partial agonist at beta-adrenergic receptors and acts as a coronary vasodilator and cardiotonic agent.
SynonymsOxyfedrine L-form hydrochloride, Modacor, Ildamen, D-563, D563, D 563
Chemical Properties
Molecular Weight349.85
FormulaC19H24ClNO3
Cas No.16777-42-7
SmilesC(CCN[C@H]([C@H](O)C1=CC=CC=C1)C)(=O)C2=CC(OC)=CC=C2.Cl
Relative Density.1.122g/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 (128.63 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8584 mL14.2918 mL28.5837 mL142.9184 mL
5 mM0.5717 mL2.8584 mL5.7167 mL28.5837 mL
10 mM0.2858 mL1.4292 mL2.8584 mL14.2918 mL
20 mM0.1429 mL0.7146 mL1.4292 mL7.1459 mL
50 mM0.0572 mL0.2858 mL0.5717 mL2.8584 mL
100 mM0.0286 mL0.1429 mL0.2858 mL1.4292 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:
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2 Enter the in vivo formulation:
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