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Pinosylvic acid

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Catalog No. T201918Cas No. 38232-09-6

Pinosylvic acid is a Pinosylvin derivative, Pinosylvin can play an antioxidant role by scavenging free radicals, inhibiting protein kinase C and other mechanisms, and has a variety of biological functions such as antifungal, antibacterial, anticancer, anti-inflammatory, antioxidant, neuroprotective, antiallergic and so on.Pinosylvic acid is a competitive inhibitor of lunularic acid decarboxylase.

Pinosylvic acid

Pinosylvic acid

😃Good
Catalog No. T201918Cas No. 38232-09-6
Pinosylvic acid is a Pinosylvin derivative, Pinosylvin can play an antioxidant role by scavenging free radicals, inhibiting protein kinase C and other mechanisms, and has a variety of biological functions such as antifungal, antibacterial, anticancer, anti-inflammatory, antioxidant, neuroprotective, antiallergic and so on.Pinosylvic acid is a competitive inhibitor of lunularic acid decarboxylase.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$195-In Stock
5 mg$483-In Stock
10 mg$692-In Stock
25 mg$1,080-In Stock
50 mg$1,490-In Stock
100 mg$1,970-In Stock
200 mg$2,690-In 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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Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Pinosylvic acid is a Pinosylvin derivative, Pinosylvin can play an antioxidant role by scavenging free radicals, inhibiting protein kinase C and other mechanisms, and has a variety of biological functions such as antifungal, antibacterial, anticancer, anti-inflammatory, antioxidant, neuroprotective, antiallergic and so on.Pinosylvic acid is a competitive inhibitor of lunularic acid decarboxylase.
In vitro
Pinosylvic acid (10µM, 20µM, 50µM) was used to treat RAW264.7 macrophages, and after LPS-induced inflammation, various Methods including the Griess assay, quantitative PCR, Western blotting, and immunofluorescence were employed for detection. The Results showed that Pinosylvic acid (10-50µM) significantly inhibited LPS-induced NO production (P<0.001), reduced the mRNA and protein expression levels of IL-1β, IL-6, and TNF-α, and inhibited the nuclear translocation of NF-κBp65. These findings suggest that Pinosylvic acid exhibits significant anti-inflammatory activity in vitro by inhibiting the NF-κB signaling pathway [1].
In vivo
In inflammation and cardiovascular disease in vivo experimental models in rats or mice, Pinosylvic acid (at doses of 10-50mg/kg) was administered via oral or intraperitoneal injection for a duration of 14-28 days. The Results showed that Pinosylvic acid significantly reduced MPO activity and levels of inflammatory markers such as TNF-α. In cardiovascular disease models, it effectively improved myocardial function and alleviated myocardial damage. Histological analysis revealed that Pinosylvic acid could reduce infiltration of inflammatory cells and tissue damage. The study confirmed that Pinosylvic acid exhibited significant anti-inflammatory effects in vivo, provided protective effects against cardiovascular diseases, and showed no apparent toxicity or side effects during the experiment, indicating good safety[2].
Chemical Properties
Molecular Weight256.25
FormulaC15H12O4
Cas No.38232-09-6
SmilesC(=C/C1=CC=CC=C1)\C2=C(C(O)=O)C(O)=CC(O)=C2
Relative Density.no data available
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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
%
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% 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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