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N-trans-Sinapoyltyramine

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Catalog No. TN4618Cas No. 200125-11-7

N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.

N-trans-Sinapoyltyramine

N-trans-Sinapoyltyramine

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Purity: 99.73%
Catalog No. TN4618Cas No. 200125-11-7
N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$248In StockIn Stock
5 mg$620In StockIn Stock
10 mg$882In StockIn Stock
25 mg$1,330In StockIn Stock
50 mg$1,780InquiryInquiry
1 mL x 10 mM (in DMSO)$630In 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:99.73%
Appearance:Solid
Color:White
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Product Introduction

N-trans-Sinapoyltyramine AI Summary
N-trans-Sinapoyltyramine is a multi-faceted chemical entity exhibiting various biological activities. It demonstrates growth inhibition against HepG2, VA13, and WI38 cells with an IC50 value greater than 20.0 µg/mL. In terms of antiproliferative efficacy, it shows limited activity against a range of human cell lines such as A549, MCF7, ZR-75-1, SK-BR-3, MDA-MB-231, DU145, KB, and KBVIN, with IC50 values exceeding 40,000.0 nM. Specific tests on human MDA-MB-231 and MDA-MB-468 cells expressing c-MET reveal IC50 values of 72,800.0 nM and 80,200.0 nM, respectively, for antiproliferative activity, and greater than 50,000.0 nM for antimigratory activity in MDA-MB-231 cells. Its antimycobacterial activity against Mycobacterium tuberculosis H37Rv shows a MIC greater than 100.0 µg/mL, indicating limited effectiveness at this concentration. Additionally, it exhibits antimicrobial properties against Streptococcus pyogenes and Staphylococcus aureus with a MIC of 62.5 µg/mL. N-trans-Sinapoyltyramine also possesses antineuroinflammatory activity, inhibiting LPS-induced NO production in mouse BV2 cells with an IC50 greater than 50,000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
Chemical Properties
Molecular Weight343.37
FormulaC19H21NO5
Cas No.200125-11-7
SmilesC(=C/C(NCCC1=CC=C(O)C=C1)=O)\C2=CC(OC)=C(O)C(OC)=C2
Relative Density.1.248 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: 55 mg/mL (160.18 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9123 mL14.5616 mL29.1231 mL145.6155 mL
5 mM0.5825 mL2.9123 mL5.8246 mL29.1231 mL
10 mM0.2912 mL1.4562 mL2.9123 mL14.5616 mL
20 mM0.1456 mL0.7281 mL1.4562 mL7.2808 mL
50 mM0.0582 mL0.2912 mL0.5825 mL2.9123 mL
100 mM0.0291 mL0.1456 mL0.2912 mL1.4562 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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