Pramiracetam
Structural formula | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
![]() |
||||||||||||||||
General | ||||||||||||||||
Non-proprietary name | Pramiracetam | |||||||||||||||
other names |
N - [2- (Diisopropylamino) ethyl] -2-oxopyrrolidine-1-acetamide ( IUPAC ) |
|||||||||||||||
Molecular formula |
|
|||||||||||||||
External identifiers / databases | ||||||||||||||||
|
||||||||||||||||
Drug information | ||||||||||||||||
ATC code | ||||||||||||||||
Drug class | ||||||||||||||||
properties | ||||||||||||||||
Molar mass | ||||||||||||||||
safety instructions | ||||||||||||||||
|
||||||||||||||||
Toxicological data |
4355 mg kg −1 ( LD 50 , mouse , oral , pramiracetam sulfate) |
|||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Pramiracetam is a drug from the group of nootropics . After traumatic brain injuries, Pramiracetam is said to improve the limited mental abilities. Its mechanism of action is largely unknown. The therapeutic use of pramiracetam is considered controversial.
Manufacturing
The synthesis takes place starting from 2-pyrrolidone in the first step by reaction with ethyl bromoacetate. In the second step, the target compound is obtained by reacting with N , N- diisopropylethylenediamine.
Individual evidence
- ↑ harmonized classification for this substance . A labeling of [No public or meaningful name is available] in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on July 11, 2020, is reproduced from a self-classification by the distributor . There is not yet a
- ↑ Entry on pramiracetam in the ChemIDplus database of the United States National Library of Medicine (NLM), accessed on July 11, 2020.
- ↑ AG Malykh, MR Sadaie: Piracetam and piracetam-like drugs: from basic science to novel clinical applications to CNS disorders . In: Drugs . tape 70 , no. 3 , February 2010, p. 287-312 , doi : 10.2165 / 11319230-000000000-00000 , PMID 20166767 .
- ↑ Donald E. Butler, Ivan C. Nordin, Yvon J. L'Italien, Lynette Zweisler, Paul H. Poschel, John G. Marriott: Amnesia-reversal activity of a series of N - [(disubstituted-amino) alkyl] - 2-oxo-1-pyrrolidine acetamides, including pramiracetam . In: Journal of Medicinal Chemistry . tape 27 , no. 5 , 1984, pp. 684-691 , doi : 10.1021 / jm00371a023 .
- ^ Axel Kleemann , Jürgen Engel, Bernd Kutscher, Dietmar Reichert: Pharmaceutical Substances. 4th edition. 2000, 2 volumes published by Thieme-Verlag Stuttgart, ISBN 978-1-58890-031-9 ; online since 2003 with biannual additions and updates.