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CB2R/FAAH modulator-1, a cannabinoid type 2 receptor (CB2R) agonist, is also a fatty acid amide hydrolase (FAAH) inhibitor (IC50=4 μM) that reduces the production of pro-inflammatory and anti-inflammatory cytokines and is commonly used in inflammation studies. The Kis for CB2R and CB1R are 14.8 nM and 241.3 nM, respectively.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
1 mg | $70 | In Stock | |
5 mg | $161 | In Stock | |
10 mg | $236 | In Stock | |
25 mg | $355 | In Stock | |
50 mg | $497 | In Stock | |
100 mg | $678 | In Stock | |
200 mg | $913 | In Stock | |
1 mL x 10 mM (in DMSO) | $166 | In Stock |
Description | CB2R/FAAH modulator-1, a cannabinoid type 2 receptor (CB2R) agonist, is also a fatty acid amide hydrolase (FAAH) inhibitor (IC50=4 μM) that reduces the production of pro-inflammatory and anti-inflammatory cytokines and is commonly used in inflammation studies. The Kis for CB2R and CB1R are 14.8 nM and 241.3 nM, respectively. |
Targets&IC50 | FAAH:4 μM, CB2 receptor:14.8 nM(Kis), CB1 receptor:241.3 nM(Kis) |
In vitro | CB2R/FAAH modulator-1 (compound 13; 10 μM; 24 h) reduces TNFα, IFN-γ, IL-1β, and IL-6 production in unstimulated monocytes and macrophages[1]. |
Molecular Weight | 361.48 |
Formula | C24H27NO2 |
Cas No. | 928892-60-8 |
Smiles | N(C(=O)C1=C(OCC2=CC=CC=C2)C=CC=C1)C34CC5CC(C3)CC(C4)C5 |
Relative Density. | 1.19 g/cm3 (Predicted) |
Storage | Shipping with blue ice. | |||||||||||||||||||||||||
Solubility Information | DMSO: 11 mg/mL (30.43 mM) | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
DMSO
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