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The drug is a phenylacetylindole and it really works being an agonist at CB1 and CB2 receptors. It's got an affinity of ~11 nM at CB1 and ~33 nM at CB2. jwh k2 powder
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As revealed from your dose response curves, all exam drugs were being fully successful uptake inhibitors at DAT and NET, with little activity at SERT, So, exhibiting catecholamine selectivity.
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