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2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid

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Catalog No. T38224Cas No. 24967-27-9

2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity against sialidases 1–4, with an IC50 of 43–143 μM, and also exhibits inhibitory activity against various influenza viruses.

2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid

2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid

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Catalog No. T38224Cas No. 24967-27-9
2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity against sialidases 1–4, with an IC50 of 43–143 μM, and also exhibits inhibitory activity against various influenza viruses.
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25 mg$5226-8 weeks6-8 weeks
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity against sialidases 1–4, with an IC50 of 43–143 μM, and also exhibits inhibitory activity against various influenza viruses.
In vitro
Methods:
To evaluate the effect on sialidase activity in pancreatic β-cells, INS-1D cells were used, and in vitro enzymatic activity was measured using the substrate 4MU-Neu5Ac (2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid).
Results:
N-acetyl-2,3-dehydro-2-deoxyneuraminic acid (DANA / Neu5Ac2en) significantly inhibited sialidase activity in INS-1D cells at concentrations ranging from 10 to 100 μM in a dose-dependent manner [1].
In vivo
Methods:
A mouse model of pulmonary fibrosis was established using bleomycin. Starting on day 10 after bleomycin administration, mice were intraperitoneally injected with 2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid (DANA) at a dose of 10 mg/kg daily. Treatment continued until day 21, at which point the animals were euthanized for tissue analysis.
Results:
Inhibition of sialidase activity starting on day 10 after bleomycin administration significantly attenuated pulmonary fibrosis, suggesting that DANA exerts anti-fibrotic effects.[1]
Chemical Properties
Molecular Weight291.26
FormulaC11H17NO8
Cas No.24967-27-9
Smiles[C@H]([C@@H](CO)O)(O)[C@]1([C@H](NC(C)=O)[C@@H](O)C=C(C(O)=O)O1)[H]
Relative Density.1.58 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMF: < 1 mg/ml (insoluble), Sonication is recommended.
DMSO: 1 mg/mL (3.43 mM), Sonication is recommended.
PBS (pH 7.2): 10 mg/mL (34.33 mM), Sonication is recommended.
Solution Preparation Table
DMSO/PBS (pH 7.2)
1mg5mg10mg50mg
1 mM3.4334 mL17.1668 mL34.3336 mL171.6679 mL
PBS (pH 7.2)
1mg5mg10mg50mg
5 mM0.6867 mL3.4334 mL6.8667 mL34.3336 mL
10 mM0.3433 mL1.7167 mL3.4334 mL17.1668 mL
20 mM0.1717 mL0.8583 mL1.7167 mL8.5834 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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%
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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

Keywords

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