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Diflubenzuron

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Catalog No. T7088Cas No. 35367-38-5
Alias Larvakil, Dimilin, Difubenzuron, Difluron

Diflubenzuron (Larvakil) is a benzoyl-urea insecticide, found to be a potent inhibitor of melanosome synthesis in mouse melanoma cells. Diflubenzuron has also been shown to inhibit TCDD-induced CYP1A1 expression in HepG2 cells.

Diflubenzuron

Diflubenzuron

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🥰Excellent
Purity: 99.96%
Catalog No. T7088Alias Larvakil, Dimilin, Difubenzuron, DifluronCas No. 35367-38-5
Diflubenzuron (Larvakil) is a benzoyl-urea insecticide, found to be a potent inhibitor of melanosome synthesis in mouse melanoma cells. Diflubenzuron has also been shown to inhibit TCDD-induced CYP1A1 expression in HepG2 cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
100 mg$48In StockIn Stock
500 mg$113In StockIn Stock
1 g$166In StockIn 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:99.96%
Appearance:Solid
Color:White
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Product Introduction

Diflubenzuron AI Summary
Diflubenzuron demonstrates a wide range of bioactivities, including significant antitumor, antiviral, insecticidal, and antifeedant properties. In vivo, it shows antitumor activity against 6C3HED lymphosarcoma with inhibition percentages of 6.0% and 33.0% at doses of 300 mg/kg and 1600 mg/kg respectively for 10 days. Additionally, it has an IC50 value of >20.0 ug/mL for inhibiting the growth of CCRF-CEM cells over 72 hours. The compound acts as an agonist for retinoid X receptor alpha, peroxisome proliferator-activated receptor gamma, Aryl hydrocarbon Receptor (AhR), and antioxidant response element (ARE) with Nrf2-dependent transcriptional activity. It also inhibits binding or entry into cells for Lassa Virus and Marburg Virus and exhibits antiviral activity against Foot and Mouth Disease Virus. In terms of insecticidal capabilities, Diflubenzuron exhibits potent activities against a variety of pests. It shows 100% mortality rates in Culex pipiens pallens mosquito larvae at 0.01 mg/L after 8 days and significant mortality in Mythimna separata (Oriental armyworm) larvae, with 100% mortality observed at 0.5 mg/L and 1 mg/L after 4 days. It is also effective against Chilo suppressalis larvae, inhibiting N-acetyl-[1-14C]glucosamine incorporation with an EC50 of 20.0 nM and inhibiting chitin synthesis with IC50 values of 19.05 nM and 20.42 nM. Moreover, Diflubenzuron effectively controls insect populations in agricultural settings, causing over 90% egg mortality in Spodoptera litura at 1 to 4 ppm and significant mortality in Plutella xylostella with an LC50 of 19.9 ug/mL in susceptible strains. However, it demonstrates reduced efficacy against fufenozide-resistant strains with a Resistance ratio of 17.2. Its toxicity is evident in Daphnia magna with an EC90 of 0.5 ppb. In summary, Diflubenzuron is highly effective as an antitumor agent, antiviral compound, and potent insecticide with varied applications across different pest species and settings..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Diflubenzuron (Larvakil) is a benzoyl-urea insecticide, found to be a potent inhibitor of melanosome synthesis in mouse melanoma cells. Diflubenzuron has also been shown to inhibit TCDD-induced CYP1A1 expression in HepG2 cells.
SynonymsLarvakil, Dimilin, Difubenzuron, Difluron
Chemical Properties
Molecular Weight310.68
FormulaC14H9ClF2N2O2
Cas No.35367-38-5
SmilesFc1cccc(F)c1C(=O)NC(=O)Nc1ccc(Cl)cc1
Relative Density.1.4301 g/cm3 (Estimated)
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: Insoluble
DMSO: 50 mg/mL (160.94 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.2187 mL16.0937 mL32.1875 mL160.9373 mL
5 mM0.6437 mL3.2187 mL6.4375 mL32.1875 mL
10 mM0.3219 mL1.6094 mL3.2187 mL16.0937 mL
20 mM0.1609 mL0.8047 mL1.6094 mL8.0469 mL
50 mM0.0644 mL0.3219 mL0.6437 mL3.2187 mL
100 mM0.0322 mL0.1609 mL0.3219 mL1.6094 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.
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