Small molecule · CNS / Psychiatric

Amphetamine

Adderall
Small moleculeCNS stimulant, triggers non-vesicular dopamine/norepinephrine release via VMAT2 displacement and transporter reversal

PubChem CID 5826 · 3D model

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Gets pulled into nerve cells by the same transporters it will later reverse, then breaks open the internal storage packets holding dopamine and norepinephrine and pumps both out into the synapse in a flood — a more forceful release mechanism than methylphenidate's simple blockade, even though both treat ADHD.

How it works

Unlike Concerta (methylphenidate), also on this site, which works by plugging up the 'drains' that normally clear dopamine and norepinephrine away, Adderall works from the inside: it hitches a ride into the nerve cell on those same drains, breaks open the internal storage packets holding dopamine and norepinephrine, and then runs the drains themselves backward, actively pumping those chemicals out into the space between nerve cells. The result is a much bigger flood of these focus-and-alertness chemicals than simply blocking reuptake would produce — a genuinely different mechanism from methylphenidate, even though both drugs are prescribed for ADHD.

What it’s used for

Adderall is prescribed to treat ADHD and narcolepsy, a condition involving excessive daytime sleepiness with sudden sleep attacks. It carries a boxed warning, the FDA's strongest safety warning, because it's a Schedule II controlled substance with real potential for abuse and addiction.

Mechanism
CNS stimulant, triggers non-vesicular dopamine/norepinephrine release via VMAT2 displacement and transporter reversal
Drug class
Therapeutic area
CNS / Psychiatric

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