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Cobalt protoporphyrin IX

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Catalog No. T78623Cas No. 14325-03-2

Cobalt Protoporphyrin IX serves as a potent, specific inducer of heme oxygenase-1 (HO-1) and demonstrates broad-spectrum antiviral effects against Influenza A virus (IAV) [1].

Cobalt protoporphyrin IX

Cobalt protoporphyrin IX

😃Good
Catalog No. T78623Cas No. 14325-03-2
Cobalt Protoporphyrin IX serves as a potent, specific inducer of heme oxygenase-1 (HO-1) and demonstrates broad-spectrum antiviral effects against Influenza A virus (IAV) [1].
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mgInquiry7-10 days7-10 days
5 mgInquiry7-10 days7-10 days
10 mgInquiry7-10 days7-10 days
25 mgInquiry7-10 days7-10 days
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Cobalt Protoporphyrin IX serves as a potent, specific inducer of heme oxygenase-1 (HO-1) and demonstrates broad-spectrum antiviral effects against Influenza A virus (IAV) [1].
In vitro
Cobalt protoporphyrin IX demonstrated maximal non-toxic concentration (TC0) of 3.13 μM in both MDCK and RAW264.7 cells after 72 hours [1]. At 2 μM, with a treatment duration ranging from 0 to 24 hours, the compound increased HO-1 intracellular protein levels in a time-dependent manner in these cells [1]. With respect to influenza viruses Empty Cell A/FortMonmouth/1/1947, A/TianjinJinnan/15/2009, A/Wuhan/359/1995, A/FujianTongan/196/2009, and BY/FujianXinluo/54/2006, Cobalt protoporphyrin IX exhibited IC50 values of 0.40 ± 0.16, 0.42 ± 0.15, 0.46 ± 0.19, 0.34 ± 0.05, and 0.64 ± 0.30 μM, respectively [1]. At concentrations ranging from 0.25-2 μM for 18 or 24 hours, the compound inhibited IAV replication by enhancing the IFN response, an antiviral activity that was independent of the catalytic function of HO-1 [1]. Additionally, at 2 μM for 0-6 hours, Cobalt protoporphyrin IX induction of HO-1 antiviral activity may be dependent on the phosphorylation and translocation of IRF3, thereby strengthening the antiviral IFN response [1].
Chemical Properties
Molecular Weight619.58
FormulaC34H32CoN4O4
Cas No.14325-03-2
SmilesC(CC([O-])=O)C=1C=2[N-]3[Co+2]45[N]6=C(C2)C(CCC([O-])=O)=C(C)C6=CC=7[N-]4C(C=C8[N]5=C(C=C3C1C)C(C=C)=C8C)=C(C=C)C7C.[H+].[H+]
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 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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