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Cannabigerol

Catalog No. TN1465 Copy Product Info
Purity: 99.92%
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Cannabigerol is a high affinity α±2-adrenergic receptor agonist, moderate affinity 5-HT1A receptor antagonist, and low affinity CB1 receptor antagonist ; also binds to the CB2 receptor; it can relieve interocular pressure, which may be of benefit in the treatment of glaucoma.

Cannabigerol

Copy Product Info
🥰Excellent
Catalog No. TN1465

Cannabigerol is a high affinity α±2-adrenergic receptor agonist, moderate affinity 5-HT1A receptor antagonist, and low affinity CB1 receptor antagonist ; also binds to the CB2 receptor; it can relieve interocular pressure, which may be of benefit in the treatment of glaucoma.

Cannabigerol
Cas No. 25654-31-3
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$148In StockIn Stock
2 mg$226In StockIn Stock
5 mg$331In StockIn Stock
10 mg$498In StockIn Stock
25 mg$851In StockIn Stock
50 mg$1,170-In Stock
100 mg$1,580-In Stock
1 mL x 10 mM (in DMSO)$341In StockIn Stock
In stock · 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:99.92%
Appearance:Solid
Color:White
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Product Introduction

Cannabigerol AI Summary
Cannabigerol exhibits a diverse range of bioactivities. It shows antibacterial activity against various methicillin-resistant and macrolide-resistant strains of Staphylococcus aureus, including specific strains like SA1199B and RN4220, with a minimum inhibitory concentration (MIC) of 1.0 ug/mL after 18 hours of exposure. This compound also targets tetracycline-resistant strains such as XU212. For epidemic strains 15 and 16 of methicillin-resistant Staphylococcus aureus, the MIC values are 2.0 ug/mL and 1.0 ug/mL, respectively. In addition to its antibacterial properties, Cannabigerol exhibits agonist activity at the rat TRPA1 channel, increasing intracellular calcium influx with an EC50 of 3400.0 nM. It interacts with cannabinoid receptors CB1 and CB2, where it displaces [3H]-CP55940 with Ki values of 153.0 nM (CB2) and 897.0 nM (CB1). The compound also affects various TRP receptors such as TRPV1, TRPV2, TRPA1, and TRPM8, exhibiting both agonist and antagonist activities, with a notable IC50 value of 160.0 nM for TRPM8 antagonism. Moreover, Cannabigerol demonstrates multiple other bioactivities: it inhibits FAAH in rat brain membranes (IC50 > 100,000 nM) and MAGL in African green monkey COS cell homogenates (IC50 95,700.0 nM). It also inhibits recombinant human DAGLalpha (IC50 > 100,000 nM) and shows an IC50 of 11,300.0 nM for the uptake of [14C]-AEA in rat RBL2H3 cells. It has agonist activity at GAL4-tagged PPARgamma with an EC50 value of 15700.0 nM and shows inhibition of human LDHB reducing lactate production by less than 50% at 10 uM. Cannabigerol also demonstrates antihemolytic potency against erythrocytes subjected to hypotonic lysis and substantial inhibition of lysophosphatidylcholine acyltransferase in mouse brains. It exhibits antibiofilm and antimicrobial activities against methicillin-resistant Staphylococcus aureus USA300 and displays antimycobacterial activity against Escherichia coli in conjunction with polymyxin..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Cannabigerol is a high affinity α±2-adrenergic receptor agonist, moderate affinity 5-HT1A receptor antagonist, and low affinity CB1 receptor antagonist ; also binds to the CB2 receptor; it can relieve interocular pressure, which may be of benefit in the treatment of glaucoma.
Chemical Properties
Molecular Weight316.48
FormulaC21H32O2
Cas No.25654-31-3
SmilesC(CCCC)C1=CC(O)=C(C/C=C(/CCC=C(C)C)\C)C(O)=C1
Relative Density.0.987g/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: 65 mg/mL (205.38 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1598 mL15.7988 mL31.5976 mL157.9879 mL
5 mM0.6320 mL3.1598 mL6.3195 mL31.5976 mL
10 mM0.3160 mL1.5799 mL3.1598 mL15.7988 mL
20 mM0.1580 mL0.7899 mL1.5799 mL7.8994 mL
50 mM0.0632 mL0.3160 mL0.6320 mL3.1598 mL
100 mM0.0316 mL0.1580 mL0.3160 mL1.5799 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
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2 Enter the in vivo formulation:
% DMSO
%
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% Saline/PBS/ddH2O

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