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Tyrosinase-IN-2

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Catalog No. T60278Cas No. 180864-33-9

Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase, a copper-containing metalloenzyme crucial for the rate-limiting step in melanin biosynthesis and enzymatic browning processes. This compound shows promise for research into skin whitening agents and food preservatives [1].

Tyrosinase-IN-2

Tyrosinase-IN-2

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Purity: 99.78%
Catalog No. T60278Cas No. 180864-33-9
Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase, a copper-containing metalloenzyme crucial for the rate-limiting step in melanin biosynthesis and enzymatic browning processes. This compound shows promise for research into skin whitening agents and food preservatives [1].
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$39In StockIn Stock
25 mg$82In StockIn Stock
50 mg$133In StockIn Stock
100 mg$215In 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:99.78%
Appearance:Solid
Color:Yellow
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Product Introduction

Tyrosinase-IN-2 AI Summary
Tyrosinase-IN-2 exhibits a wide range of bioactivities against several parasites and enzymes, showing significant potential as an anti-parasitic and multi-target therapeutic agent. It demonstrates anti-parasitic activity against Toxoplasma gondii, reducing the number of intracellular parasites in infected vero cells, with IC50 values of 1,500,000 nM and 500,000 nM for the infected cells and parasites, respectively. The compound also inhibits the trypomastigote and amastigote stages of Trypanosoma cruzi Y, with EC50 values of 1,430.0 nM and 3,230.0 nM, respectively, and selectivity indices of 26.2 and 11.6, indicating specificity towards the parasite over mammalian cells. Additionally, Tyrosinase-IN-2 shows various inhibitory activities: against jack bean urease (IC50 547.0 nM, Ki 497.0 nM), mushroom tyrosinase (IC50 1740.0 nM for diphenolase and 50.0 nM for monophenolase), and human ERG, along with inhibition of human microsomal CYP enzymes and recombinant human aurora B kinase. It also addresses multiple bacterial and viral targets, including inhibition of AmpC Beta-Lactamase, ROR gamma transcriptional activity, and Vaccinia Orthopoxvirus. The compound exhibits cytotoxicity against different human cell lines but also potentiates methotrexate-induced antitrypanosomal activity and displays permeability in PAMPA assays. This diverse bioactivity profile hints at its potential utility in treating multiple diseases, particularly parasitic infections..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase, a copper-containing metalloenzyme crucial for the rate-limiting step in melanin biosynthesis and enzymatic browning processes. This compound shows promise for research into skin whitening agents and food preservatives [1].
Chemical Properties
Molecular Weight224.24
FormulaC8H8N4O2S
Cas No.180864-33-9
SmilesNC(=S)N\N=C\c1ccc(cc1)[N+]([O-])=O
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: 50 mg/mL (222.98 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.4595 mL22.2975 mL44.5951 mL222.9754 mL
5 mM0.8919 mL4.4595 mL8.9190 mL44.5951 mL
10 mM0.4460 mL2.2298 mL4.4595 mL22.2975 mL
20 mM0.2230 mL1.1149 mL2.2298 mL11.1488 mL
50 mM0.0892 mL0.4460 mL0.8919 mL4.4595 mL
100 mM0.0446 mL0.2230 mL0.4460 mL2.2298 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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%
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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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