Product name:Pramiracetam
Appearance:White powder
Assay: 99%
Chemical name:N-[2-(diisopropylamino)ethyl]-2-oxo-1-pyrrolidineacetamide

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Product Description

Description Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramiracetam reportedly improved cognitive deficits associated with traumatic brain injuries. Pramiracetam sulfate did not exhibit any affinity in vitro for dopaminergic , GABAergic, serotoninergic, adrenergic, muscarinic, adenosine (IC50 > 10 uM), and benzodiazepine receptors (IC50 > 1 uM) binding sites [1].in vivo: In a double-blind, randomized design, two groups of six subjects each received alternating placebo and single 400, 800, 1,200, and 1,600 mg oral doses of pramiracetam after an overnight fast. Mean (+/- SD) peak plasma concentrations of the four dose groups (2.71 +/- 0.54, 5.40 +/- 1.34, 6.13 +/- 0.71, 8.98 +/- 0.71 micrograms/mL) were attained between two to three hours following drug administration [2]. Two doses of pramiracetam (7.5 mg/kg and 15 mg/kg) were administered daily prior to testing for 7 weeks in a 16-arm radial maze in which nine arms were baited with food [3].
Density 1.0±0.1 g/cm3
Boiling Point 461.0±30.0 °C at 760 mmHg
Molecular Formula C14H27N3O2
Molecular Weight 269.383
Flash Point 232.6±24.6 °C
Exact Mass 269.210327
PSA 52.65000
LogP 0.39
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.495
Storage condition 2-8°C

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