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Avicularin

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Catalog No. T6S0117Cas No. 572-30-5
Alias Fenicularin

Avicularin (Fenicularin) has anti-allergic, anti-inflammatory, hepatoprotective, antioxidant, anti-tumor and other activities. It ameliorates human hepatocellular carcinoma by modulating the activities of NF-κB(p65), COX-2, and PPAR-γ. In LPS-stimulated RAW 264.7 macrophages, it exerts anti-inflammatory activity by inhibiting the ERK signaling pathway.

Avicularin

Avicularin

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Purity: 99.94%
Catalog No. T6S0117Alias FenicularinCas No. 572-30-5
Avicularin (Fenicularin) has anti-allergic, anti-inflammatory, hepatoprotective, antioxidant, anti-tumor and other activities. It ameliorates human hepatocellular carcinoma by modulating the activities of NF-κB(p65), COX-2, and PPAR-γ. In LPS-stimulated RAW 264.7 macrophages, it exerts anti-inflammatory activity by inhibiting the ERK signaling pathway.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$53In StockIn Stock
5 mg$98In StockIn Stock
10 mg$163In StockIn Stock
25 mg$297In StockIn Stock
50 mg$439In StockIn Stock
100 mg$648-In Stock
200 mg$925-In Stock
1 mL x 10 mM (in DMSO)$113In 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:99.94%
Color:White to Yellow
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Product Introduction

Avicularin AI Summary
Avicularin exhibits a multifaceted profile of bioactivity across various biological systems. It inhibits cow milk xanthine oxidase activity by 30.8% at a concentration of 50 µg/mL and demonstrates notable procoagulant inhibition in human monocytes by counteracting IL1-induced tissue factor expression at 10 µM after 18 hours, resulting in 0.0 microunits of tissue factor per 10^5 cells. The compound is also effective against algae, showing antialgal activity with IC50 values of 180,000.0 nM for Microcystis aeruginosa NIES 44 and 28,000.0 nM for Anabaena flos-aquae NIES 73. Additionally, Avicularin inhibits human recombinant aldose reductase (IC50: 19050.0 nM) and chicken liver Fatty Acid Synthase (FASN) (IC50: 6150.0 nM). It also has antiviral activity against the Dengue virus, with an IC50 of 1700.0 nM, and shows cytotoxicity against human cancer cell lines SGC7901, A549, and HeLa with IC50 values >10.0 µg/mL. Furthermore, it has potent antioxidant activity, with DPPH and ABTS radical scavenging IC50 values of 16.13 µg/mL and 6.9 µg/mL, respectively, and exhibits increasing FRAP values at higher concentrations (25, 50, and 100 µg/mL). The compound displays antifungal properties with minimum inhibitory concentrations (MIC) of 2.0 µg/mL against Candida albicans and Aspergillus fumigatus ATTC 26934, and 8.0 µg/mL against Candida parapsilosis. Lastly, Avicularin acts as an agonist at TRPA1 channels with 41.0% activity at 1000 µM relative to AITC..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Avicularin (Fenicularin) has anti-allergic, anti-inflammatory, hepatoprotective, antioxidant, anti-tumor and other activities. It ameliorates human hepatocellular carcinoma by modulating the activities of NF-κB(p65), COX-2, and PPAR-γ. In LPS-stimulated RAW 264.7 macrophages, it exerts anti-inflammatory activity by inhibiting the ERK signaling pathway.
SynonymsFenicularin
Chemical Properties
Molecular Weight434.35
FormulaC20H18O11
Cas No.572-30-5
SmilesOC[C@@H]1O[C@@H](Oc2c(oc3cc(O)cc(O)c3c2=O)-c2ccc(O)c(O)c2)[C@H](O)[C@H]1O
Relative Density.1.86 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature,keep 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
H2O: 1.15 mg/mL (2.65 mM), Sonication is recommended.
DMSO: 120 mg/mL (276.27 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.3023 mL11.5115 mL23.0229 mL115.1145 mL
DMSO
1mg5mg10mg50mg
5 mM0.4605 mL2.3023 mL4.6046 mL23.0229 mL
10 mM0.2302 mL1.1511 mL2.3023 mL11.5115 mL
20 mM0.1151 mL0.5756 mL1.1511 mL5.7557 mL
50 mM0.0460 mL0.2302 mL0.4605 mL2.3023 mL
100 mM0.0230 mL0.1151 mL0.2302 mL1.1511 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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