Clinical data | |
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Trade names | Breinox, Dinagen, Lucetam, Nootropil, Nootropyl, Oikamid, Piracetam, others |
AHFS/Drugs.com | International Drug Names |
Routes of administration | By mouth, parenteral, inhalation |
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Pharmacokinetic data | |
Bioavailability | ~100% |
Onset of action | Swiftly following administration. Food delays time to peak concentration by 1.5 h approximately to 2–3 h since dosing.[2] |
Elimination half-life | 4–5 hours |
Excretion | Urinary |
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ECHA InfoCard | 100.028.466 |
Chemical and physical data | |
Formula | C6H10N2O2 |
Molar mass | 142.158 g·mol−1 |
3D model (JSmol) | |
Melting point | 152 °C (306 °F) |
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Piracetam is a drug that has efficacy in cognitive disorders, vertigo, cortical myoclonus, dyslexia, and sickle cell anemia; sources differ on its usefulness for dementia.[3][4][5] Piracetam is sold as a medication in many European countries. Sale of piracetam is not illegal in the United States, although it is not regulated nor approved by the FDA, so it is legally sold for research use only.[6]
Piracetam is in the racetams group, with chemical name 2-oxo-1-pyrrolidine acetamide. It is a cyclic derivative of the neurotransmitter GABA[4] and shares the same 2-oxo-pyrrolidone base structure with pyroglutamic acid. Related drugs include the anticonvulsants levetiracetam and brivaracetam, and the putative nootropics aniracetam and phenylpiracetam.
(eMC) 2017
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