Piracetam

Synonyms: UCB 6215

Piracetam (UCB 6215) is a cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA), used in treatment of a wide range of cognitive disorders.

Piracetam Chemical Structure

Piracetam Chemical Structure

CAS: 7491-74-9

Purity & Quality Control

Batch: S307001 DMSO] 72 mg/mL] false] Water] 72 mg/mL] false] Ethanol] Insoluble] false Purity: 100%
100

Piracetam Related Products

Choose Selective GABA Receptor Inhibitors

Biological Activity

Description Piracetam (UCB 6215) is a cyclic derivative of the neurotransmitter gamma-aminobutyric acid (GABA), used in treatment of a wide range of cognitive disorders.
Targets
AMPA receptor [1]
In vitro
In vitro Piracetam is able to significantly decrease the fusogenic and destabilising effect of Abeta 29-42, in a concentration-dependent manner. Preincubation of piracetam, at a piracetam/peptide ratio of 960, during 20 min before the addition of Abeta 29-42 prevents almost completely the mixture of the two fluorescent probes. Preincubation of piracetam with lipids prevents almost completely the release of calcein induced by the peptide in a dose-dependent fashion (piracetam/peptide ratios from 9.6 to 960). [1] Piracetam (< 1.0 mM) preincubated with brain membranes enhances membrane fluidity in aged mice, rats and humans, as indicated by decreased anisotropy of the membrane-bound fluorescence probe 1,6-diphenyl-1,3,5-hexatriene (DPH). [2]
In Vivo
In vivo Piracetam (300 mg/kg once daily) significantly increases membrane fluidity in some brain regions of young and aged rats, but has no measurable effect on membrane fluidity in the young rats. [2] Piracetam (300 mg/kg daily for 6 weeks) improves active avoidance learning in the aged rats only and elevates membrane fluidity in all brain regions except the cerebellum in the aged rats. Piracetam (300 mg/kg daily for 6 weeks) also improves NMDA receptor density in the hippocampus and on muscarinic cholinergic receptor densities in the frontal cortex and the striatum and to a lesser extent in the hippocampus of rats. [3] Piracetam (500 mg/kg p.o. for 14 days) elevates N-methyl-D-aspartate (NMDA) receptor density by about 20% and normalizes the enhanced affinity of L-glutamate for the NMDA receptor in aged mice. [4] Piracetam-treated withdrawn rats has higher the number of synapses than that observed in nonpiracetam-treated and alcohol-fed animals by up to 20%, the mechanisms leading to the synaptic reorganization took place at the mossy fiber level. [5]
Animal Research Animal Models male Wistar rats
Dosages 300 mg/kg
Administration Orally
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05918341 Not yet recruiting
Drug Adherence Marker
The Netherlands Cancer Institute
July 3 2023 Phase 4
NCT00567060 Completed
Memory Disorders
UCB Pharma
May 2000 Not Applicable

Chemical Information & Solubility

Molecular Weight 142.16 Formula

C6H10N2O2

CAS No. 7491-74-9 SDF Download Piracetam SDF
Smiles C1CC(=O)N(C1)CC(=O)N
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 72 mg/mL ( (506.47 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 72 mg/mL

Ethanol : Insoluble


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In vivo
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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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