Pivagabine structure
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Common Name | Pivagabine | ||
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CAS Number | 69542-93-4 | Molecular Weight | 187.23600 | |
Density | 1.053g/cm3 | Boiling Point | 397ºC at 760 mmHg | |
Molecular Formula | C9H17NO3 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 193.9ºC |
Use of PivagabinePivagabine (CXB 722), a psychoactive drug, is a hydrophobic 4-aminobutyric acid derivative with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor function and corticotropin-releasing factor (CRF) concentrations in rat brain[1][2]. |
Name | 4-Pivalamidobutanoic acid |
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Synonym | More Synonyms |
Description | Pivagabine (CXB 722), a psychoactive drug, is a hydrophobic 4-aminobutyric acid derivative with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor function and corticotropin-releasing factor (CRF) concentrations in rat brain[1][2]. |
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Related Catalog | |
In Vivo | Pivagabine (CXB 722) (200 mg/kg; i.p.; twice a day for 4 days and 1 hour before killing on the 5th day) prevents the effects of foot-shock stress on CRF concentration in both brain regions[2]. Animal Model: Adult male Sprague-Dawley CD rats (200-250 g)[2] Dosage: 200 mg/kg Administration: i.p.; twice a day for 4 days and 1 hour before killing on the 5th day Result: Prevented the effects of foot-shock stress on CRF concentration in both brain regions. Reduced by 52% the CRF concentration in the hypothalamus but had no effect on that in the cerebral cortex. |
References |
Density | 1.053g/cm3 |
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Boiling Point | 397ºC at 760 mmHg |
Molecular Formula | C9H17NO3 |
Molecular Weight | 187.23600 |
Flash Point | 193.9ºC |
Exact Mass | 187.12100 |
PSA | 69.89000 |
LogP | 1.85380 |
Index of Refraction | 1.462 |
Storage condition | 2-8°C |
4-(2,2-dimethylpropanoylamino)butanoic acid |