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Kurarinone

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Catalog No. T5S0993Cas No. 34981-26-5

Kurarinone is a flavonoid extracted from the shrub Sophora flavescens, which has anti-tumor, estrogenic and anti-inflammatory activities, and also has a strong inhibitory effect on immune responses.

Kurarinone

Kurarinone

😃Good
Purity: 99.72%
Catalog No. T5S0993Cas No. 34981-26-5
Kurarinone is a flavonoid extracted from the shrub Sophora flavescens, which has anti-tumor, estrogenic and anti-inflammatory activities, and also has a strong inhibitory effect on immune responses.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$39In StockIn Stock
5 mg$122In StockIn Stock
10 mg$197In StockIn Stock
25 mg$455In StockIn Stock
50 mg$657In StockIn Stock
100 mg$918-In Stock
500 mg$1,830InquiryInquiry
1 mL x 10 mM (in DMSO)$135In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.72%
Appearance:Solid
Color:Yellow to Orange
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Product Introduction

Bioactivity
Description
Kurarinone is a flavonoid extracted from the shrub Sophora flavescens, which has anti-tumor, estrogenic and anti-inflammatory activities, and also has a strong inhibitory effect on immune responses.
In vitro
METHODS: To test the cytotoxicity of kurarinone on HMC3 cells, we treated HMC3 cells with different concentrations of kurarinone (10, 20, 40 or 80 μM) for 24 hours.
RESULTS HMC3 cell viability was reduced after treatment with 80 μM Kur.
METHODS: Two human small cell lung cancer (SCLC) cell lines H1688 and H146, and an immortalized bronchial epithelial cell line BEAS-2B were treated with different concentrations of kurarinone (3.125 ~ 50 μM), and the IC50 was determined.
RESULTS The IC50 values of kurarinone against H1688, H146 and BEAS-2B cells were 12.5±4.7, 30.4±5.1 and 55.8±4.9 μM respectively. [3]
In vivo
METHODS: Arthritis was reproduced in DBA/1 mice by inducing bovine type II collagen (CII) as a collagen-induced arthritis (CIA) model. After establishment of CIA, kurarinone (100 mg/kg/day) was administered orally from day 21 to day 42, and severity was determined based on symptom scoring scales and histopathology. ELISA and flow cytometry were used to detect the cytokine levels, anti-cii antibody levels, and T cell proliferation and lineage in the draining lymph nodes, respectively.
RESULTS kurarinone treatment reduced the severity of arthritis in CIA mice and reduced the levels of pro-inflammatory cytokines TNF-α, IL-6, IFN-γ and IL-17A in serum and foot tissue. [1]
Chemical Properties
Molecular Weight438.51
FormulaC26H30O6
Cas No.34981-26-5
SmilesCOc1cc(O)c(C[C@@H](CC=C(C)C)C(C)=C)c2O[C@@H](CC(=O)c12)c1ccc(O)cc1O
Relative Density.1.266g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 235 mg/mL (535.91 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.56 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 mM2.2804 mL11.4022 mL22.8045 mL114.0225 mL
5 mM0.4561 mL2.2804 mL4.5609 mL22.8045 mL
10 mM0.2280 mL1.1402 mL2.2804 mL11.4022 mL
20 mM0.1140 mL0.5701 mL1.1402 mL5.7011 mL
50 mM0.0456 mL0.2280 mL0.4561 mL2.2804 mL
100 mM0.0228 mL0.1140 mL0.2280 mL1.1402 mL

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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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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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