Chemical Structure | ![]() |
Drug Class | Atypical phenylalkylamine / Dopaminergic |
Mechanisms of action |
SERT robust inhibition / release DAT inhibition / release Low NET activity Weak TAAR1 interaction possible |
Monograph |
Chemical Name: Biphenylamphetamine Development: First synthesized in the 40s. Structural Interest: Biphenyl substitution increases steric bulk and rigidity. BPMA is probably more fat-soluble due to the lipophilic amine, making it easier to pass the blood-brain barrier-and presenting a faster onset and shorter action. Modern Interest:The compound is being evaluated for its potential role in dry stimulation - enhanced wakefulness and performance without classic amphetamine euphoria. Non-euphoric dopaminergics in cognitive and motivational settings. Anorexiant stimulant. |
Synthesis batch initiated | 1 gram target |Amount acquired for synthesis purposes: 10 g |Amount acquired for speculative holding: 5 g Note: These figures reflect total documented acquisitions. Updated manually |
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