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Isobavachalcone

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Catalog No. T3861Cas No. 20784-50-3
Alias Isobacachalcone, Corylifolinin

Isobavachalcone (Corylifolinin) is a chalcone constituent of Angelica keiskei, has potent anti-inflammatory activity, possible can ameliorate neuronal injury in brain diseases associated with inflammation.

Isobavachalcone

Isobavachalcone

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Purity: 99.76%
Catalog No. T3861Alias Isobacachalcone, CorylifolininCas No. 20784-50-3
Isobavachalcone (Corylifolinin) is a chalcone constituent of Angelica keiskei, has potent anti-inflammatory activity, possible can ameliorate neuronal injury in brain diseases associated with inflammation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$55In StockIn Stock
10 mg$93In StockIn Stock
25 mg$197In StockIn Stock
50 mg$293In StockIn Stock
100 mg$437In Stock-
500 mg$982InquiryInquiry
1 mL x 10 mM (in DMSO)$61In 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:99.76%
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Product Introduction

Isobavachalcone AI Summary
Isobavachalcone exhibits a broad spectrum of bioactivities across different biological targets and organisms. It demonstrates antifungal activity against Candida albicans and Cryptococcus neoformans with IC50 values of 3.0 µg/mL and 7.0 µg/mL, respectively. The compound also shows antibacterial activity against multiple strains, including methicillin-resistant Staphylococcus aureus, Bacillus subtilis, and Escherichia coli, with varying minimum inhibitory concentration (MIC) values. Additionally, it exhibits antiprotozoal activity against Bodo caudatus with an LC50 value of 4.36 µg/mL after 48 hours. Isobavachalcone displays significant inhibition of collagen-induced, arachidonic acid-induced, and platelet-activating factor-induced platelet aggregation in rabbit platelets, with IC50 values indicating high effectiveness. It also inhibits nitric oxide production in mouse RAW264.7 cells with an IC50 value of 1600 nM and shows anti-inflammatory properties by inhibiting NF-kappaB transactivation and LPS-induced nitric oxide production. Moreover, Isobavachalcone demonstrates cytotoxicity in various human cancer cell lines, including Raji, K562, A549, MCF7, and THP1 cells, with IC50 values indicating potent antitumor activity. It activates the Nrf2 pathway in HepG2 cells, suggesting cytoprotective properties, and inhibits enzymes such as human PTP1B and porcine pancreatic lipase with significant IC50 values. The compound also exhibits antioxidant activity and has strong inhibitory effects on SARS-CoV papain-like protease and human DHODH. Its potential in inhibiting fungal, bacterial, and viral targets along with its anti-inflammatory, cytotoxic, and antiproliferative activities make Isobavachalcone a promising candidate for further pharmacological research and development..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Isobavachalcone (Corylifolinin) is a chalcone constituent of Angelica keiskei, has potent anti-inflammatory activity, possible can ameliorate neuronal injury in brain diseases associated with inflammation.
Targets&IC50
OVCAR-8 cells:7.92 μM (IC50)
SynonymsIsobacachalcone, Corylifolinin
Chemical Properties
Molecular Weight324.37
FormulaC20H20O4
Cas No.20784-50-3
SmilesCC(C)=CCc1c(O)ccc(C(=O)\C=C\c2ccc(O)cc2)c1O
Relative Density.1.243g/cm3
Storage & Solubility Information
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 58.82 mg/mL (181.34 mM), Sonication is recommended.
Chloroform, Dichloromethane, Ethyl Acetate, Acetone: Soluble
In Vivo Formulation
10% DMSO+90% Saline: 2.5 mg/mL (7.71 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 mM3.0829 mL15.4145 mL30.8290 mL154.1450 mL
5 mM0.6166 mL3.0829 mL6.1658 mL30.8290 mL
10 mM0.3083 mL1.5414 mL3.0829 mL15.4145 mL
20 mM0.1541 mL0.7707 mL1.5414 mL7.7072 mL
50 mM0.0617 mL0.3083 mL0.6166 mL3.0829 mL
100 mM0.0308 mL0.1541 mL0.3083 mL1.5414 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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