ID: selegiline
Aliases: L-deprenyl, EMSAM
Type: compound
Route/form: oral/transdermal depending product
Status: approved
Evidence level: approved / labelled
Best data tier: approved label
Support scope: human, review/regulatory
Source types: label, review
Linked sources: 3
Broad outcomes: Brain / mood / sleep
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- irreversible MAO-B inhibitor
- MAO-A inhibition at higher exposures
Optimization domains
- Parkinsons
- depression
- MAOI
Research basis
- Selegiline has approved oral Parkinson and transdermal depression contexts, making it the cleanest practical MAO-B anchor in the repository.
- Route matters: oral low-dose MAO-B selectivity and transdermal antidepressant MAOI exposure have different interaction and tyramine-risk profiles.
- It is relevant to optimization discussions because dopamine, energy, libido, mood, and stimulant-combination narratives often converge on MAO-B inhibition.
Limits, risks, and missing evidence
- MAOI interaction risk is serious, especially with SSRIs, clomipramine, trazodone, stimulants, dextromethorphan, opioids, sympathomimetics, and some foods depending on dose/route.
- Insomnia, anxiety, orthostasis, hypertensive reactions, serotonin toxicity, and amphetamine-like metabolites can matter.
- Using it as a casual nootropic or stimulant potentiator is a poor risk frame.
Risk flags
- approved drug
- maoi
- route dependent
- serotonin toxicity
- hypertensive crisis
- interaction risk
Linked papers, labels, and reviews
- Transdermal selegiline for the treatment of major depressive disorder
review / pubmed_selegiline_transdermal_2009
Selegiline transdermal system and MAOI dietary interaction context. - FDA label for selegiline hydrochloride orally disintegrating tablets
label / fda_selegiline_label
Official drug label. - DailyMed label: EMSAM selegiline transdermal system
label / dailymed_emsam_label
Official label for transdermal selegiline in major depressive disorder; useful for route-dependent MAOI risk.