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Marrubiin

Catalog No. TN1914 Copy Product Info
Purity: 99.81%
🥰Excellent
Marrubiin is a natural terpenoid compound extracted from Marrubium vulgare that exhibits vasodilatory and anti-edematous effects, as well as anti-inflammatory, antioxidant, and antibacterial bioactivity.

Marrubiin

Copy Product Info
🥰Excellent
Catalog No. TN1914

Marrubiin is a natural terpenoid compound extracted from Marrubium vulgare that exhibits vasodilatory and anti-edematous effects, as well as anti-inflammatory, antioxidant, and antibacterial bioactivity.

Marrubiin
Cas No. 465-92-9
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$77-In Stock
5 mg$163-In Stock
10 mg$289-In Stock
25 mg$519-In Stock
1 mL x 10 mM (in DMSO)$179-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.81%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Marrubiin is a natural terpenoid compound extracted from Marrubium vulgare that exhibits vasodilatory and anti-edematous effects, as well as anti-inflammatory, antioxidant, and antibacterial bioactivity.
In vitro
Method: Marrubiin at various concentrations (0.0001–0.001 M) was preincubated with lipoxygenase (8000 U/mL) for 5 minutes. Sodium linoleate was then added as a substrate, and changes in absorbance were continuously monitored at 234 nm to calculate the inhibition rate.
Results: Marrubiin exhibited moderate inhibitory activity against LOX (IC50 = 173 μg/mL). [1]
Methods: Human umbilical vein endothelial cells (HUVECs) were pretreated with marrubiin (39 µM) for 24 hours, then stimulated with TNF-α (50 ng/mL) for 24 hours; GSH levels were measured using a glutathione assay kit.
Results: Pretreatment with marrubiin significantly increased GSH levels and antagonized the depleting effect of TNF-α, indicating that marrubiin protects endothelial cells by maintaining cellular antioxidant reserves.[2]
In vivo
Methods: Inflammation was induced in C57BL/6 mice by intraperitoneal injection of carrageenan (1%, 250 μL). Marrubiin (1, 10, 20, 40 mg/kg) was administered intraperitoneally 1 hour prior to carrageenan stimulation, and the animals were sacrificed 4 hours after carrageenan stimulation.
Results: Marrubiin dose-dependently reduced the total number of inflammatory cells in the exudate, significantly decreased protein content and MPO activity in the exudate, and maintained or increased GPx activity, but had no significant effect on GSH levels. [1]
Chemical Properties
Molecular Weight332.43
FormulaC20H28O4
Cas No.465-92-9
SmilesC[C@@]12[C@]3([C@](OC(=O)[C@@]3(C)CCC1)(C[C@@H](C)[C@@]2(CCC=4C=COC4)O)[H])[H]
Relative Density.1.152 g/cm3 at 20℃
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: 80 mg/mL (240.65 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0082 mL15.0408 mL30.0815 mL150.4076 mL
5 mM0.6016 mL3.0082 mL6.0163 mL30.0815 mL
10 mM0.3008 mL1.5041 mL3.0082 mL15.0408 mL
20 mM0.1504 mL0.7520 mL1.5041 mL7.5204 mL
50 mM0.0602 mL0.3008 mL0.6016 mL3.0082 mL
100 mM0.0301 mL0.1504 mL0.3008 mL1.5041 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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

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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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