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CB1/2 agonist 3

Catalog No. T61736Cas No. 2772655-86-2

CB1/2 agonist 3 is a competitive and potent CB1/CB2 agonist with high affinity for hCB1 and hCB2 and can be used to study neurological disorders.

CB1/2 agonist 3

CB1/2 agonist 3

Catalog No. T61736Cas No. 2772655-86-2
CB1/2 agonist 3 is a competitive and potent CB1/CB2 agonist with high affinity for hCB1 and hCB2 and can be used to study neurological disorders.
Pack SizePriceAvailabilityQuantity
1 mg$35In Stock
5 mg$81In Stock
10 mg$133In Stock
25 mg$218In Stock
50 mg$325In Stock
100 mg$483In Stock
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Product Introduction

Bioactivity
Description
CB1/2 agonist 3 is a competitive and potent CB1/CB2 agonist with high affinity for hCB1 and hCB2 and can be used to study neurological disorders.
Targets&IC50
CB2-CHO cells (human):1.28 nM (EC50), CP-55940:78.17 nM (Kb), CB1-CHO cells (human):30.99 nM (EC50)
In vitro
CB1/2 agonist 3 partially induced the binding of [35S]GTPγS to hCB1-CHO cell membranes with an EC50=30.99 nM and slightly inhibited the binding of [35S]GTPγS to hCB2-CHO cell membranes with an average EC50=1.28 nM. CB1/2 agonist 3, after treatment for 1 hour at a concentration of 1 μM , antagonized the CB1/CB2 agonist CP-55940 with Kb=78.17 nM. [1]
Chemical Properties
Molecular Weight387.6
FormulaC25H41NO2
Cas No.2772655-86-2
Storage & Solubility Information
Storagekeep away from moisture | Shipping with blue ice.
Solubility Information
DMSO: 8 mg/mL(20.64 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5800 mL12.8999 mL25.7998 mL128.9990 mL
5 mM0.5160 mL2.5800 mL5.1600 mL25.7998 mL
10 mM0.2580 mL1.2900 mL2.5800 mL12.8999 mL
20 mM0.1290 mL0.6450 mL1.2900 mL6.4499 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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