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Stimulant drug of the Amphetamine family. Reported as having Effects similar to those of Dextroamphetamine, but with a milder euphoria and a comparatively smoother comedown. Has a shorter duration and less empathogenic effect-profile as compared with 4-FA. Thought not to have some of the neurotoxic metabolites Amphetamine can produce.

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We worked since 2009 year, when JWH-018, MDPV, 4-MMC etc was legal. But nowadays, many years after we gladly offer new research chemicals such as AB-FUBINACA, AB-PINACA and of course a-pvp, 5f-akb48

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URB597 is a potent and selective inhibitor of fatty acid amide hydrolase (FAAH), the enzyme that hydrolyzes anandamide (AEA; Item No. 90050) and other simple esters and amides with long unsaturated acyl chains (IC50 = 4.6 nM and 0.5 nM in brain membranes and intact neurons, respectively).1,2 The marked depression of FAAH activity in FAAH(-/-) mice results in reduced sensation of pain and enhanced endocannabinoid signaling.3 URB597 exhibits both anti-nociceptive and anxiolytic effects in vivo without evoking other symptoms associated with cannabinoid-like compounds. Thus, URB597 may serve as a lead compound for the development of new analgesic and anxiolytic drugs.

Research Chemical

Research chemicals are drugs with relatively little history of human use, and thus particular care should be taken if choosing to ingest them

Stimulants excite the nervous system and increase physiological function.

Dose Oral

Light               0.25-0.5mg
Common   0.5-1.5mg
Strong              1.5mg+

Duration         Oral 5-15 HOURS          

Onset              Oral Minutes
After Effect      5-10 hours 

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Minimum Order Quantity (MOQ)= 10 grams

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