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Fangchinoline

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Catalog No. T3122Cas No. 436-77-1
Alias Tetrandrine B, Hanfangichin B, (+)-Limacine, (+)-Fangchinoline

Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore.

Fangchinoline

Fangchinoline

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🥰Excellent
Purity: 99.86%
Catalog No. T3122Alias Tetrandrine B, Hanfangichin B, (+)-Limacine, (+)-FangchinolineCas No. 436-77-1
Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$40In StockIn Stock
10 mg$62In StockIn Stock
25 mg$97In StockIn Stock
50 mg$139In StockIn Stock
100 mg$213In StockIn Stock
200 mg$318In StockIn Stock
1 mL x 10 mM (in DMSO)$54In 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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Batch Information

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Purity:99.86%
Appearance:Solid
Color:White
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Product Introduction

Fangchinoline AI Summary
Fangchinoline exhibits diverse and significant bioactivities. It inhibits formyl-methionyl-leucyl-phenylalanine-induced superoxide generation in PMNC with an inhibition rate of 82.4%, indicating potential anti-inflammatory properties and regulation of oxidative stress and immune responses. It inhibits COX1 with an IC50 of 129,000.0 nM and shows cytotoxicity against various human cancer cell lines, including KB, MCF-7, and K562, with varying IC50 values. The compound also demonstrates strong antiplasmodial activity against both chloroquine-sensitive and chloroquine-resistant Plasmodium falciparum, with IC50 values of 179.0 nM and 306.0 nM, respectively. It exhibits antiamoebic activity against Entamoeba histolytica (IC50 = 14.71 ug/mL) and antibacterial activity against methicillin-resistant Staphylococcus aureus (MIC = 6.0 ug/mL). In addition, Fangchinoline induces rat C/EBPalpha expression in human U937 cells, increases Rhodamine 123 accumulation in HCT15 cells, and shows significant antiviral activity against SARS-CoV-2 in HEK293T cells with an IC50 of 193.0 nM. Despite its broad cytotoxic and inhibitory effects, it displays low cytotoxicity against certain cell lines and does not significantly inhibit AKT activity (IC50 > 20000.0 nM). Moreover, it has moderate selectivity indices in antiplasmodial assays, suggesting a balance between efficacy and cytotoxicity..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Fangchinoline (Tetrandrine B) is extracted from Stephania tetrandra S. Moore.
SynonymsTetrandrine B, Hanfangichin B, (+)-Limacine, (+)-Fangchinoline
Chemical Properties
Molecular Weight608.72
FormulaC37H40N2O6
Cas No.436-77-1
SmilesCOc1ccc2C[C@H]3N(C)CCc4cc(OC)c(O)c(Oc5cc6[C@H](Cc7ccc(Oc1c2)cc7)N(C)CCc6cc5OC)c34
Relative Density.1.204 g/cm3 (Predicted)
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: 49.5 mg/mL (81.32 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.29 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 mM1.6428 mL8.2140 mL16.4279 mL82.1396 mL
5 mM0.3286 mL1.6428 mL3.2856 mL16.4279 mL
10 mM0.1643 mL0.8214 mL1.6428 mL8.2140 mL
20 mM0.0821 mL0.4107 mL0.8214 mL4.1070 mL
50 mM0.0329 mL0.1643 mL0.3286 mL1.6428 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
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

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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