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Herbacetin

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Catalog No. T5S1331Cas No. 527-95-7

1. Herbacetin induces apoptosis in HepG2 cells, by ROS and PI3K/Akt pathway. 2. Herbacetin suppresses the HGF-induced motility of human breast cancer MDA-MB-231 cells by inhibiting c-Met and Akt phosphorylation.

Herbacetin

Herbacetin

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Purity: 99.51%
Catalog No. T5S1331Cas No. 527-95-7
1. Herbacetin induces apoptosis in HepG2 cells, by ROS and PI3K/Akt pathway. 2. Herbacetin suppresses the HGF-induced motility of human breast cancer MDA-MB-231 cells by inhibiting c-Met and Akt phosphorylation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$39In StockIn Stock
5 mg$89In StockIn Stock
10 mg$147In StockIn Stock
25 mg$312In StockIn Stock
50 mg$468-In Stock
1 mL x 10 mM (in DMSO)$97In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.51%
Color:Yellow
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Product Introduction

Herbacetin AI Summary
Herbacetin exhibits significant antiviral activity against influenza A viruses, specifically H9N2 and H1N1 strains, by reducing virus-induced cytopathic effects with EC50 values of 23000.0 nM and 35000.0 nM, respectively. It functions as a noncompetitive inhibitor of recombinant influenza A virus neuraminidase, with Ki and IC50 values of 13700.0 nM and 8900.0 nM, respectively, and also inhibits Clostridium perfringens neuraminidase with an IC50 value of 1400.0 nM. The compound shows selectivity indexes of 8.39 for H1N1 and 12.77 for H9N2, as calculated by the ratio of CC50 for MDCK cells to EC50 for the influenza viruses. Additionally, Herbacetin demonstrates bioactivity as an inhibitor of human liver FBP1, with an IC50 value of 8700.0 nM. It also inhibits key viral proteases, showing an IC50 value of 33100.0 nM for SARS-CoV 3C-like protease and 33000.0 nM for SARS-CoV-2 3CL protease, both measured using FRET assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. Herbacetin induces apoptosis in HepG2 cells, by ROS and PI3K/Akt pathway. 2. Herbacetin suppresses the HGF-induced motility of human breast cancer MDA-MB-231 cells by inhibiting c-Met and Akt phosphorylation.
Chemical Properties
Molecular Weight302.24
FormulaC15H10O7
Cas No.527-95-7
SmilesOc1ccc(cc1)-c1oc2c(O)c(O)cc(O)c2c(=O)c1O
Relative Density.1.799g/cm3
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 150 mg/mL (496.29 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.62 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 mM3.3086 mL16.5431 mL33.0863 mL165.4314 mL
5 mM0.6617 mL3.3086 mL6.6173 mL33.0863 mL
10 mM0.3309 mL1.6543 mL3.3086 mL16.5431 mL
20 mM0.1654 mL0.8272 mL1.6543 mL8.2716 mL
50 mM0.0662 mL0.3309 mL0.6617 mL3.3086 mL
100 mM0.0331 mL0.1654 mL0.3309 mL1.6543 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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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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

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