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Isoferulic acid

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Catalog No. T2889Cas No. 537-73-5
Alias Isoferulate, Hesperetic acid, Hesperetate, 3-Hydroxy-4-methoxycinnamic acid

Isoferulic acid (Hesperetate) exhibits hypoglycemic properties.

Isoferulic acid

Isoferulic acid

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Purity: 99.49%
Catalog No. T2889Alias Isoferulate, Hesperetic acid, Hesperetate, 3-Hydroxy-4-methoxycinnamic acidCas No. 537-73-5
Isoferulic acid (Hesperetate) exhibits hypoglycemic properties.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$40-In Stock
1 g$64-In Stock
1 mL x 10 mM (in DMSO)$29In 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:99.49%
Appearance:Solid
Color:White
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Product Introduction

Isoferulic acid AI Summary
Isoferulic acid is a bioactive molecule that demonstrates a range of biological activities. It inhibits the diphenolase activity of mushroom tyrosinase at a concentration of 0.035 mM, with an inhibition of 7.9%, and shows an IC50 of 115,200.0 nM in a different mushroom tyrosinase inhibition assay. Although it exhibits antiproliferative activity against various cell lines including mouse B16-BL6, human HT1080, human A549, human HeLa, and mouse 26-L5 cells, its EC50 values are consistently greater than 515,000.0 nM, indicating low potency in cell proliferation inhibition. In terms of cytotoxicity, it shows an IC50 value greater than 10,000.0 nM against human HeLa cells and greater than 50,000.0 nM in anti-inflammatory assays involving mouse RAW264.7 cells. The compound inhibits hyaluronidase with an IC50 value greater than 2,000,000.0 nM and alpha-amylase with an IC50 value greater than 7,000,000.0 nM. It also exhibits antioxidant activities with an EC50 value greater than 250,000.0 nM in DPPH radical scavenging assays. Additionally, Isoferulic acid shows estrogenic activity, acting on the ERalpha receptor in human MVLN cells, achieving substantial luciferase reporter gene expression at concentrations of 20 and 100 μg/mL. In ion channel assays, it exhibits strong inhibition (98.5%) of the Gloeobacter violaceus ligand-gated ion channel expressed in Xenopus laevis oocytes, with an antagonist IC50 value of 13,500.0 nM. The compound is also cytoprotective against H2O2-induced cytotoxicity in human EAhy926 cells, with an EC50 of 29,300.0 nM for protective effects. It exhibits antitrypanosomal activity against Trypanosoma brucei brucei Lister 427 bloodstream forms, with an IC50 value of less than 30,000.0 nM. Furthermore, Isoferulic acid shows varied bioactivities across several specific assays, including inhibition of Chronic Active B-Cell Receptor Signaling (6513.1 nM), ELG1-dependent DNA repair (25,918.5 nM), HP1-beta Chromodomain interactions (100,000.0 nM), acting as an agonist of gsp for Fibrous Dysplasia/McCune-Albright Syndrome (3981.1 nM), and inhibiting human tyrosyl-DNA phosphodiesterase 1 (TDP1) in cells in the presence of CPT (29,092.9 nM)..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Isoferulic acid (Hesperetate) exhibits hypoglycemic properties.
Targets&IC50
α1-adrenoceptor:1.4 µM (EC50), β-endorphin:52.2 nM (EC50)
SynonymsIsoferulate, Hesperetic acid, Hesperetate, 3-Hydroxy-4-methoxycinnamic acid
Chemical Properties
Molecular Weight194.18
FormulaC10H10O4
Cas No.537-73-5
SmilesCOC1=C(O)C=C(\C=C\C(O)=O)C=C1
Relative Density.1.0583 g/cm3 (Estimated)
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (257.49 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (10.3 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 mM5.1499 mL25.7493 mL51.4986 mL257.4930 mL
5 mM1.0300 mL5.1499 mL10.2997 mL51.4986 mL
10 mM0.5150 mL2.5749 mL5.1499 mL25.7493 mL
20 mM0.2575 mL1.2875 mL2.5749 mL12.8747 mL
50 mM0.1030 mL0.5150 mL1.0300 mL5.1499 mL
100 mM0.0515 mL0.2575 mL0.5150 mL2.5749 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

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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