pramiracetam

Modify Date: 2024-01-04 19:38:57

pramiracetam Structure
pramiracetam structure
Common Name pramiracetam
CAS Number 68497-62-1 Molecular Weight 269.383
Density 1.0±0.1 g/cm3 Boiling Point 461.0±30.0 °C at 760 mmHg
Molecular Formula C14H27N3O2 Melting Point 47 °C
MSDS Chinese USA Flash Point 232.6±24.6 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of pramiracetam


Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramiracetam reportedly improved cognitive deficits associated with traumatic brain injuries. IC50 Value: Target: in vitro: 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].

 Names

Name Pramiracetam Hydrate
Synonym More Synonyms

 pramiracetam Biological Activity

Description Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramiracetam reportedly improved cognitive deficits associated with traumatic brain injuries. IC50 Value: Target: in vitro: 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].
Related Catalog
References

[1]. Warner Lambert, et al. Some Neurochemical Properties of Pramiracetam (CI-879), A New Cognition-Enhancing Agent.

[2]. Chang T, et al. Pharmacokinetics of oral pramiracetam in normal volunteers. J Clin Pharmacol. 1985 May-Jun;25(4):291-5.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 461.0±30.0 °C at 760 mmHg
Melting Point 47 °C
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

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Hazard Codes Xn
Risk Phrases 22
RIDADR NONH for all modes of transport
HS Code 2942000000

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2933790090
Summary 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0%

 Articles23

More Articles
The effects of cholinergic drugs support an avoidance learning hypothesis of brief footshock-induced analgesia.

Neuropharmacology 25(10) , 1161-6, (1986)

Rats were tested for tail-flick responses and then immediately subjected to footshock for 30 sec. This procedure induced analgesia, i.e. prolonged the latency of the tail-flick response, which was max...

The memory-enhancing effects of the piracetam-like nootropics are dependent on experimental parameters.

Behav. Brain Res. 33(1) , 79-82, (1989)

The effects of the nootropic agent piracetam and its congeners oxiracetam, pramiracetam and aniracetam on the retention performance of mice in a passive-avoidance situation are dependent on the intens...

Gas chromatographic assay of pramiracetam in human plasma using nitrogen specific detection.

J. Chromatogr. A. 274 , 346-9, (1983)

 Synonyms

N-[2-[di(propan-2-yl)amino]ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
Neupramir
Pramiracetam
Pramistar
Remen
Amacetam
N-[2-(Diisopropylamino)ethyl]-2-(2-oxo-1-pyrrolidinyl)acetamide
1-Pyrrolidineacetamide, N-[2-[bis(1-methylethyl)amino]ethyl]-2-oxo-
MFCD00867219
N-[2-(diisopropylamino)ethyl]-2-oxo-1-pyrrolidineacetamide
N-[2-(dipropan-2-ylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
N-[2-[Bis(1-methylethyl)amino]ethyl]-2-oxo-1-pyrrolidineacetamide
N-[2-(Diisopropylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
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