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Norartocarpetin

Catalog No. T72803 Copy Product Info
Purity: 99.97%
🥰Excellent
Norartocarpetin is a tyrosinase inhibitor with strong inhibitory activity against tyrosinase (IC₅₀ = 0.47 μM). It can be used as an anti-browning agent in food-related research and also shows significant anti-tumor activity against human lung cancer NCI-H460 cells with an IC₅₀ of 22 μM. Its anti-proliferative mechanisms mainly include regulating the Ras/Raf/MAPK signaling pathway, inducing mitochondria-dependent apoptosis, arresting the cell cycle at S phase, and inhibiting cell migration and invasion.

Norartocarpetin

Copy Product Info
🥰Excellent
Catalog No. T72803

Norartocarpetin is a tyrosinase inhibitor with strong inhibitory activity against tyrosinase (IC₅₀ = 0.47 μM). It can be used as an anti-browning agent in food-related research and also shows significant anti-tumor activity against human lung cancer NCI-H460 cells with an IC₅₀ of 22 μM. Its anti-proliferative mechanisms mainly include regulating the Ras/Raf/MAPK signaling pathway, inducing mitochondria-dependent apoptosis, arresting the cell cycle at S phase, and inhibiting cell migration and invasion.

Norartocarpetin
Cas No. 520-30-9
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$113-In Stock
5 mg$289-In Stock
10 mg$479-In Stock
25 mg$892-In Stock
50 mg$1,220-In Stock
1 mL x 10 mM (in DMSO)$273-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.97%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Norartocarpetin is a tyrosinase inhibitor with strong inhibitory activity against tyrosinase (IC₅₀ = 0.47 μM). It can be used as an anti-browning agent in food-related research and also shows significant anti-tumor activity against human lung cancer NCI-H460 cells with an IC₅₀ of 22 μM. Its anti-proliferative mechanisms mainly include regulating the Ras/Raf/MAPK signaling pathway, inducing mitochondria-dependent apoptosis, arresting the cell cycle at S phase, and inhibiting cell migration and invasion.
Targets&IC50
Tyrosinase:0.47 μM, NCI-H460 cells:22 μM
In vitro
Methods: Relevant cells were treated with Norartocarpetin to detect its mushroom tyrosinase inhibitory activity; NCI-H460 and MRC-9 cells were treated with different concentrations of Norartocarpetin for 24–48 h to detect cytotoxicity, signaling pathways, apoptosis, cell cycle, invasion and migration.
Results:
1 Norartocarpetin had potent mushroom tyrosinase inhibitory activity with an IC₅₀ of 0.47 μM [1].
2 Norartocarpetin (0–100 μM, 48 h) showed dose-dependent cytotoxicity on NCI-H460 and MRC-9 cells, with IC₅₀ values of 22 μM and 85 μM, respectively.
3 Norartocarpetin (0, 11, 22, 44 μM, 24 h) could block the Ras/Raf/MAPK signaling pathway.
4 Norartocarpetin (0, 11, 22, 44 μM, 24 h) could induce apoptosis in human lung cancer NCI-H460 cells.
5 Norartocarpetin (0, 11, 22, 44 μM) could induce cell cycle arrest at the S phase.
6 Norartocarpetin (22 μM, 24 h) could inhibit cell invasion in a dose-dependent manner.
7 Norartocarpetin (0, 11, 22, 44 μM, 24 h) could significantly inhibit cell migration [2].
Chemical Properties
Molecular Weight286.24
FormulaC15H10O6
Cas No.520-30-9
SmilesO=C1C=C(OC=2C=C(O)C=C(O)C12)C=3C=CC(O)=CC3O
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (279.49 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4936 mL17.4679 mL34.9357 mL174.6786 mL
5 mM0.6987 mL3.4936 mL6.9871 mL34.9357 mL
10 mM0.3494 mL1.7468 mL3.4936 mL17.4679 mL
20 mM0.1747 mL0.8734 mL1.7468 mL8.7339 mL
50 mM0.0699 mL0.3494 mL0.6987 mL3.4936 mL
100 mM0.0349 mL0.1747 mL0.3494 mL1.7468 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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