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| Cat. No. : | HY-103338 |
| M.Wt: | 409.60 |
| Formula: | C27H39NO2 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
AM1172 is metabolically stable anandamide uptake inhibitor. AM1172 inhibits [3H] anandamide transport in rat cortical neurons and human CCF-STTG1 astrocytoma cells with IC50 values of 2.1 μM and 2.5 μM, respectively. AM1172 can significantly inhibit AEA hydrolysis and concurrently decrease AEA uptake. AM1172 can be used for the study of endocannabinoid system regulation[1][2][3].
In Vitro:AM1172 inhibits [3H] anandamide transport in rat cortical neurons and human CCF-STTG1 astrocytoma cells with IC50 values of 2.1 μM and 2.5 μM, respectively[1].
AM1172 (10-30 μM, 5 min) significantly reduces [14C]AEA hydrolysis in RBL-2H3 cells and concurrently decreases [14C]AEA uptake[2].
AM1172 shows moderate affinities for G protein-coupled CB1(IC50 = 271 nM) and CB2 receptors (IC50 = 189 nM)[3].
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