LSD (Lysergic Acid Diethylamide)
Potent semi-synthetic ergoline psychedelic and 5-HT2A partial agonist. Active at microgram doses. Despite its short plasma half-life (~3.6h), subjective effects last 8-12 hours, likely due to prolonged receptor binding ("lid" trapping). Metabolite O-H-LSD is the primary urinary marker.
Projected serum levels — 1 tabs (≈ 0.10 mg), as needed (shown daily)
Maintenance schedule: 1 tabs (≈ 0.10 mg) as needed (shown daily) (oral).
Modeled steady state after ~1 days: peak ≈ 0.054 mg, trough ≈ 0.001 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Psychedelic
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 3.6 h
- Common dose
- 1 tabs (≈ 0.10 mg)
- Reference dose range
- 0.50–2 tabs (single dose)
- Suggested cadence
- as needed (shown daily)
- Validated against
- 0.20 mg oral — Cmax 0.004 mg/L at 1.5 h
Documented interactions
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danger
1P-LSD (1-Propionyl-LSD) + LSD (Lysergic Acid Diethylamide)
1P-LSD (1-Propionyl-LSD) and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).
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danger
25I-NBOMe + LSD (Lysergic Acid Diethylamide)
25I-NBOMe and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).
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danger
2C-I (2,5-Dimethoxy-4-iodophenethylamine) + LSD (Lysergic Acid Diethylamide)
2C-I (2,5-Dimethoxy-4-iodophenethylamine) and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered…
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danger
2C-B (4-Bromo-2,5-dimethoxyphenethylamine) + LSD (Lysergic Acid Diethylamide)
2C-B (4-Bromo-2,5-dimethoxyphenethylamine) and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered…
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danger
3-MeO-PCP (3-Methoxyphencyclidine) + LSD (Lysergic Acid Diethylamide)
3-MeO-PCP (3-Methoxyphencyclidine) and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental…
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danger
4-AcO-DMT (Psilacetin) + LSD (Lysergic Acid Diethylamide)
4-AcO-DMT (Psilacetin) and LSD (Lysergic Acid Diethylamide) both have serotonergic activity. Risk of serotonin syndrome (hyperthermia, rigidity, autonomic instability, altered mental status).
Serum checks 205 modeled interaction pairings for lsd (lysergic acid diethylamide) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Pharmacokinetics and Pharmacodynamics of Lysergic Acid Diethylamide in Healthy Subjects
Landmark PK/PD study of 100 and 200 mcg oral LSD showing plasma half-life of 3.6 hours with dose-proportional kinetics and subjective effects lasting 8-12 hours.
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Pharmacokinetics and Concentration-Effect Relationship of Oral LSD in Humans
First modern controlled PK study of LSD showing rapid absorption (Tmax ~1.5h), elimination half-life of 3.6h up to 12h, and prolonged effects beyond plasma elimination due to receptor binding.
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Pharmacokinetics and Pharmacodynamics of Lysergic Acid Diethylamide Microdoses in Healthy Participants
Characterized microdose (5-20 mcg) LSD pharmacokinetics showing elimination half-lives of 2.5-2.9 hours with dose-proportional plasma concentrations.
3 published studies referenced in the app, each with a plain-language summary.