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(-)-Catechin gallate

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Catalog No. T3682Cas No. 130405-40-2
Alias (-)-Catechin 3-O-gallate, (-)-Catechin 3-gallate

(-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of 6PGD, IDH. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of human Beta-secretase. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) possesses antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum NF54 and chloroquine-resistant Plasmodium falciparum K1.

(-)-Catechin gallate

(-)-Catechin gallate

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🥰Excellent
Purity: 97.74%
Catalog No. T3682Alias (-)-Catechin 3-O-gallate, (-)-Catechin 3-gallateCas No. 130405-40-2
(-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of 6PGD, IDH. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of human Beta-secretase. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) possesses antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum NF54 and chloroquine-resistant Plasmodium falciparum K1.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$68In StockIn Stock
5 mg$213In StockIn Stock
10 mg$338In StockIn Stock
25 mg$493In StockIn Stock
50 mg$621In StockIn Stock
100 mg$932In StockIn Stock
1 mL x 10 mM (in DMSO)$197In 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:97.74%
Color:White to Red
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Product Introduction

(-)-Catechin gallate AI Summary
(-)-Catechin gallate exhibits diverse bioactivities including inhibition of key enzymes and receptors. It inhibits human Beta-secretase 1 with an IC50 value of 6000.0 nM. Furthermore, it shows potent inhibition of FabZ, FabI, and FabG with respective IC50 values of 400.0 nM, 300.0 nM, and 1000.0 nM, demonstrating bioactivity in fatty acid biosynthesis pathways. The compound has notable antiplasmodial activity against chloroquine-sensitive and chloroquine-resistant Plasmodium falciparum strains with IC50 values of 3200.0 nM and 400.0 nM, respectively. Additionally, (-)-Catechin gallate acts as an antagonist at human mu, delta, and kappa opioid receptors with Ke values of 210.0 nM, 950.0 nM, and 220.0 nM, respectively. It inhibits yeast G6PD, 6PGD, and IDH with IC50 values of 240.0 nM, 1280.0 nM, and 6620.0 nM, respectively, and shows an inhibitory IC50 of 25000.0 nM for G6PD-mediated NADPH production in mouse 3T3-L1 cells. Moreover, the compound inhibits the chymotrypsin-like activity of the purified human 20S proteasome with an IC50 value of 124.0 nM and inhibits duck liver FASN with an IC50 value of 3400.0 nM. It also exhibits antioxidant properties by inhibiting lipid peroxidation in a liposomal model. (-)-Catechin gallate shows inhibition of alpha-synuclein filament formation and SARS-CoV nucleocapsid protein with IC50 values of 21400.0 nM and 0.005 µg/mL, respectively. It inhibits PKM2 activity with an IC50 value of 850.0 nM and DYRK1A activity with an IC50 value of 220.0 nM. Finally, it inhibits SIRT6 deacetylase activity with an IC50 value of 2500.0 nM, demonstrating significant multi-target inhibitory characteristics..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
(-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of 6PGD, IDH. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) displays inhibition of human Beta-secretase. (-)-Catechin gallate ((-)-Catechin 3-O-gallate) possesses antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum NF54 and chloroquine-resistant Plasmodium falciparum K1.
Synonyms(-)-Catechin 3-O-gallate, (-)-Catechin 3-gallate
Chemical Properties
Molecular Weight442.37
FormulaC22H18O10
Cas No.130405-40-2
SmilesOc1cc(O)c2C[C@@H](OC(=O)c3cc(O)c(O)c(O)c3)[C@@H](Oc2c1)c1ccc(O)c(O)c1
Relative Density.1.8 g/cm3
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 (113.03 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.52 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 mM2.2606 mL11.3028 mL22.6055 mL113.0276 mL
5 mM0.4521 mL2.2606 mL4.5211 mL22.6055 mL
10 mM0.2261 mL1.1303 mL2.2606 mL11.3028 mL
20 mM0.1130 mL0.5651 mL1.1303 mL5.6514 mL
50 mM0.0452 mL0.2261 mL0.4521 mL2.2606 mL
100 mM0.0226 mL0.1130 mL0.2261 mL1.1303 mL

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In Vivo Formulation Calculator (Clear solution)

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:
mg/kg
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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