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Medicines > classes : Antiparkinsonian or Classic Psychedelic or Sedative-Hypnotic

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generic:
brand:
None (79) · (none, never marketed) (1) · Akineton (1) · Apokyn (1) · Artane (1) · Azilect (1) · Cogentin (1) · Comtan (1) · Dalmane (1) · Delysid (historical, Sandoz, withdrawn 1965) (1) · Doral (1) · Doriden (1) · Dostinex (1) · Eldepryl (1) · Halcion (1) · Hetlioz (1) · Imovane (1) · Lunesta (1) · Mogadon (1) · Nembutal (1) · Neupro (1) · Ongentys (1) · Parlodel (1) · Placidyl (1) · ProSom (1) · Quaalude (1) · Restoril (1) · Rohypnol (1) · Rozerem (1) · Seconal (1) · Sinemet (1) · Sonata (1) · Symmetrel (1) · Tasmar (1) · THIP (1) · Versed (1) · Xadago (1) · Xyrem (1)
classes: (Click arrow to add another value)
mechanism:
5-HT2A agonist (26) · GABAA positive allosteric modulator (15) · Potent 5-HT2A agonist (5) · LSD analogue; 5-HT2A agonist (4) · Prodrug of LSD; 5-HT2A agonist (4) · GABAA positive allosteric modulator (non-benzodiazepine) (3) · None (2) · Contains LSA (2) · Contains mescaline (2) · GABAA potentiator and direct activator (2) · Irreversible selective MAO-B inhibitor (2) · Melatonin receptor agonist (2)
uses:
None (115) · No approved medical problem. Encountered as a designer/research benzodiazepine and, increasingly, as an adulterant in illicit opioid supplies. (1)
starting dose:
None (115) · No medical dose. Active recreational doses reported in the 0.5–1.5 mg range (similar potency to alprazolam). (1)
preparations:
None (115) · Illicit tablets ("bars"), powders, blotter, occasionally solutions. No pharmaceutical product exists. (1)
fda max:
None (115) · N/A (never approved) (1)
routes:
None (114) · intranasal; rectal and IV reported. (1) · Oral (2) · sublingual (1)
onset:
None (114) · 30–60 minutes (1) · ~20–40 min PO; faster sublingual/intranasal. (1)
duration:
None (114) · 6–10 h subjective; full pharmacologic effect considerably longer. (1) · 8–12 hours (1)
halflife:
None (114) · 3–5 hours (1) · Estimated ~12–17 h (some sources cite up to ~21 h); active metabolites prolong effect. (1)
bioavailability:
None (114) · 70–90% (oral) (1) · Not formally characterized in humans. (1)
pregnancy:
None (114) · Avoid. Benzodiazepines are associated with neonatal sedation, floppy-infant syndrome, and withdrawal; teratogenic signal weak but non-zero. Designer benzo with no safety data, assume worst-case. (1) · Not established (1)
legal:
None (115) · Schedule I (United States) (1)

Showing below up to 116 results in range #1 to #116.

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