Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

Isoangustone A

Copy Product Info
😃Good
Catalog No. TN4263Cas No. 129280-34-8

Isoangustone A is a natural product that inhibits PI3K, MKK4, and MKK7 through ATP competition, suppresses the expression of G1 phase regulatory proteins, inhibits the phosphorylation of Akt, GSK-3β, and JNK1/2, and inhibits the proliferation of human melanoma cells and tumour growth in xenograft mouse models.

Isoangustone A

Isoangustone A

Copy Product Info
😃Good
Purity: 98.89%
Catalog No. TN4263Cas No. 129280-34-8
Isoangustone A is a natural product that inhibits PI3K, MKK4, and MKK7 through ATP competition, suppresses the expression of G1 phase regulatory proteins, inhibits the phosphorylation of Akt, GSK-3β, and JNK1/2, and inhibits the proliferation of human melanoma cells and tumour growth in xenograft mouse models.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$229-In Stock
5 mg$577-In Stock
10 mg$822-In Stock
25 mg$1,230-In Stock
50 mg$1,680-In Stock
Add to Cart
Add to Quotation
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.
Questions
TargetMol
View More

Batch Information

Select Batch
Purity:98.89%
Appearance:Solid
Color:White
Contact us for more batch information

Resource Download

Product Introduction

Bioactivity
Description
Isoangustone A is a natural product that inhibits PI3K, MKK4, and MKK7 through ATP competition, suppresses the expression of G1 phase regulatory proteins, inhibits the phosphorylation of Akt, GSK-3β, and JNK1/2, and inhibits the proliferation of human melanoma cells and tumour growth in xenograft mouse models.
In vitro
Method:
A cell proliferation assay was performed using the SK-MEL-28 cell line. Cells were treated with Isoangustone A at concentrations of 10 μM and 20 μM for 48 and 72 hours to evaluate its effect on cell proliferation.

Result:
Isoangustone A significantly inhibited the proliferation of SK-MEL-28 cells in a dose- and time-dependent manner. [1]
In vivo
Method:
A SK-MEL-28 xenograft tumor model was established using male Balb/c nude (nu/nu) mice. Mice were administered Isoangustone A via daily intraperitoneal injection at doses of 2 or 10 mg/kg for 35 consecutive days to evaluate its antitumor effects.

Result:
Isoangustone A significantly reduced tumor weight compared to the control group. It also markedly decreased the expression of proliferating cell nuclear antigen (PCNA) and reduced the phosphorylation levels of Akt. [1]
Chemical Properties
Molecular Weight422.47
FormulaC25H26O6
Cas No.129280-34-8
SmilesO=C1C(=COC2=CC(O)=C(C(O)=C12)CC=C(C)C)C=3C=C(O)C(O)=C(C3)CC=C(C)C
Relative Density.1.31g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

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

You can also refer to dose conversion for different animals. More Dose Conversion

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

Keywords

Related Tags: buy Isoangustone A | purchase Isoangustone A | Isoangustone A cost | order Isoangustone A | Isoangustone A chemical structure | Isoangustone A in vivo | Isoangustone A in vitro | Isoangustone A formula | Isoangustone A molecular weight