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Benzyl cinnamate

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Catalog No. T8145Cas No. 103-41-3
Alias Cinnamic acid benzyl ester, Cinnamein, Benzylcinnamoate, Benzyl 3-phenylpropenoate

Benzyl cinnamate (Benzylcinnamoate) is a natural product isolated from various plant species,with anti-inflammatory activity.

Benzyl cinnamate

Benzyl cinnamate

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Purity: 99.77%
Catalog No. T8145Alias Cinnamic acid benzyl ester, Cinnamein, Benzylcinnamoate, Benzyl 3-phenylpropenoateCas No. 103-41-3
Benzyl cinnamate (Benzylcinnamoate) is a natural product isolated from various plant species,with anti-inflammatory activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$30-In Stock
1 g$44-In Stock
5 g$98-In Stock
10 g$148-In Stock
1 mL x 10 mM (in DMSO)$35-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.77%
Appearance:Solid
Color:White
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Product Introduction

Benzyl cinnamate AI Summary
Benzyl cinnamate exhibits a diverse range of bioactivities, demonstrating substantial potential for therapeutic and pesticidal applications. It shows inhibitory activity against 17 beta-hydroxysteroid dehydrogenase-catalyzed reactions, with IC50 values of 700.0 nM and 7000.0 nM for oxidation and reduction, respectively. Additionally, this compound functions as an antagonist on the HA-tagged mouse AT1a angiotensin 2 receptor in HEK293T cells, decreasing angiotensin 2-induced intracellular calcium uptake with an IC50 value of 47.2 µg/mL. In terms of pesticidal properties, Benzyl cinnamate is effective against Dermatophagoides pteronyssinus, showcasing an EC50 value of 0.18 g/m² after 24 hours. It also displays cytotoxic activity against human PANC1 cells under nutrient-deprived conditions with a PC50 value greater than 100.0 µM. Furthermore, the compound demonstrates inhibitory activity towards Histone Lysine Methyltransferase G9a with a potency of 31622.8 nM, and acts as a delayed death inhibitor of the malarial parasite plastid with a potency of 19011.5 nM. It also inhibits USP1/UAF1 with a potency of 10000.0 nM, and affects NPC function in a biochemical firefly luciferase enzyme assay with a potency of 14381.8 nM. Benzyl cinnamate exhibits anti-inflammatory effects by inhibiting TNF-alpha-induced ICAM1 protein expression in HUVEC cells, with a 50% inhibition in the first assay and an IC50 value of 70.0 µg/mL in a second assay. It is also cytotoxic to HUVEC cells, maintaining around 95% cell viability at a maximum tolerated dose of 70.0 µg/mL..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Benzyl cinnamate (Benzylcinnamoate) is a natural product isolated from various plant species,with anti-inflammatory activity.
SynonymsCinnamic acid benzyl ester, Cinnamein, Benzylcinnamoate, Benzyl 3-phenylpropenoate
Chemical Properties
Molecular Weight238.28
FormulaC16H14O2
Cas No.103-41-3
SmilesC(=CC(OCC1=CC=CC=C1)=O)C2=CC=CC=C2
Relative Density.1.183. Temperature:20 °C.
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 (209.84 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (8.39 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 mM4.1967 mL20.9837 mL41.9674 mL209.8372 mL
5 mM0.8393 mL4.1967 mL8.3935 mL41.9674 mL
10 mM0.4197 mL2.0984 mL4.1967 mL20.9837 mL
20 mM0.2098 mL1.0492 mL2.0984 mL10.4919 mL
50 mM0.0839 mL0.4197 mL0.8393 mL4.1967 mL
100 mM0.0420 mL0.2098 mL0.4197 mL2.0984 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:
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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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