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PAN endonuclease-IN-3

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Catalog No. T210780

PAN endonuclease-IN-3 is a potent inhibitor of PAN endonuclease, with an IC50 of 17.4 nM against the influenza virus polymerase complex. It demonstrates strong antiviral activity against various strains of current influenza viruses while exhibiting very low cytotoxicity in MDCK cells. In mice models infected with A/WSN/33, PAN endonuclease-IN-3 significantly suppresses viral replication.

PAN endonuclease-IN-3

PAN endonuclease-IN-3

😃Good
Catalog No. T210780
PAN endonuclease-IN-3 is a potent inhibitor of PAN endonuclease, with an IC50 of 17.4 nM against the influenza virus polymerase complex. It demonstrates strong antiviral activity against various strains of current influenza viruses while exhibiting very low cytotoxicity in MDCK cells. In mice models infected with A/WSN/33, PAN endonuclease-IN-3 significantly suppresses viral replication.
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Product Introduction

Bioactivity
Description
PAN endonuclease-IN-3 is a potent inhibitor of PAN endonuclease, with an IC50 of 17.4 nM against the influenza virus polymerase complex. It demonstrates strong antiviral activity against various strains of current influenza viruses while exhibiting very low cytotoxicity in MDCK cells. In mice models infected with A/WSN/33, PAN endonuclease-IN-3 significantly suppresses viral replication.
In vitro
PAN endonuclease-IN-3 (Compound 39-(S)) exhibits IAV polymerase inhibitory activity in HEK-293T cells with an IC₅₀ value of 17.4 nM, comparable to Baloxavir (IC₅₀ = 17.8 nM). PAN endonuclease-IN-3 (1-103 nM) strongly inhibits PAN endonuclease with an IC₅₀ of 41.8 nM. Additionally, in the MDCK cell line, PAN endonuclease-IN-3 (46 μL/well, 72 h) demonstrates exceptional antiviral activity with an EC₅₀ of 0.21 nM.
In vivo
PAN endonuclease-IN-3 (20 mg/kg, Intranasal administration, single dose) suppresses viral replication of the A/WSN/33 virus in the lungs of infected mice.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
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