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Pinosylvin

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Catalog No. T3843Cas No. 22139-77-1
Alias 5-Styrylresorcinol, 3,5-stilbenediol

Pinosylvin (5-Styrylresorcinol) induces autophagy via AMPK activation. Pinosylvin is likely to act as a pro-angiogenic factor.

Pinosylvin

Pinosylvin

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Purity: 99.91%
Catalog No. T3843Alias 5-Styrylresorcinol, 3,5-stilbenediolCas No. 22139-77-1
Pinosylvin (5-Styrylresorcinol) induces autophagy via AMPK activation. Pinosylvin is likely to act as a pro-angiogenic factor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$38In StockIn Stock
10 mg$54In StockIn Stock
25 mg$88In StockIn Stock
50 mg$129In StockIn Stock
100 mg$189In StockIn Stock
200 mg$283-In Stock
1 mL x 10 mM (in DMSO)$42In 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:99.91%
Appearance:Solid
Color:White
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Product Introduction

Pinosylvin AI Summary
Pinosylvin inhibits the protein-tyrosine kinase p56lck in vitro with an IC50 value of 193,000 nM using angiotensin I and [gamma-32P]-ATP. It also inhibits PGE-2 production in LPS-stimulated RAW264.7 cells with an IC50 value of 10,600 nM, and demonstrates significant anti-inflammatory effects in mouse J774 cells by reducing LPS-induced nitric oxide production, IL6 expression, and MCP1 expression, with IC50 values of 16,600 nM, 32,100 nM, and 38,700 nM, respectively. In addition, it shows ABTS and DPPH radical scavenging activities, displaying a trolox equivalent antioxidant capacity of 2.04 and a DPPH absorbance ratio of 0.52 relative to L-cysteine at 20 μM. The compound also exhibits antimicrobial activity against methicillin-resistant Staphylococcus aureus with MIC values of 125 μg/mL against S. aureus strains 5 and COL. It induces apoptosis in human HL60 cells, with 36.95% cell accumulation at the sub-G1 phase after 48 hours at 200 μM. Furthermore, Pinosylvin inhibits leukotriene formation in activated human neutrophils with an IC50 of 22,700 nM and demonstrates cytotoxicity against mouse Hepa 1c1c7 cells with a cell viability of 61% at 12.5 μM after 24 hours. It possesses various antioxidant activities, inhibiting AAPH-induced peroxidation and Cu2+-induced human LDL peroxidation, and delaying lipid oxidation based on the Rancimat method. The compound shows potent modulation of TRPV1 and TRPA1 receptors, serving as both an inhibitor and agonist with respective IC50 and efficacy values. Additionally, it inhibits sodium fluorescein uptake in OATP1B3 and OATP1B1-transfected CHO cells, with respective inhibition percentages of 114.57% and 133.48% at 10 μM. Pinosylvin is characterized by a log P value of 2.25, indicating moderate lipophilicity which may influence its bioavailability and efficacy..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Pinosylvin (5-Styrylresorcinol) induces autophagy via AMPK activation. Pinosylvin is likely to act as a pro-angiogenic factor.
Synonyms5-Styrylresorcinol, 3,5-stilbenediol
Chemical Properties
Molecular Weight212.24
FormulaC14H12O2
Cas No.22139-77-1
SmilesOc1cc(O)cc(\C=C\c2ccccc2)c1
Relative Density.1.252g/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: 122.5 mg/mL (577.18 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.42 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 mM4.7116 mL23.5582 mL47.1165 mL235.5824 mL
5 mM0.9423 mL4.7116 mL9.4233 mL47.1165 mL
10 mM0.4712 mL2.3558 mL4.7116 mL23.5582 mL
20 mM0.2356 mL1.1779 mL2.3558 mL11.7791 mL
50 mM0.0942 mL0.4712 mL0.9423 mL4.7116 mL
100 mM0.0471 mL0.2356 mL0.4712 mL2.3558 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

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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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