Product Description
Description
Phenibut (fenibut, phenybut; brand names Noofen and Citrocard), contracted from β-phenyl-γ-aminobutyric acid (β-phenyl-GABA), is a central depressant and analog of the inhibitory neurotransmitter γ-aminobutyric acid (GABA), or a GABA analogue. The addition of a phenyl ring allows phenibut to cross the blood-brain barrier. Phenibut was developed in the Soviet Union in the 1960s, and has since been used there as a pharmaceutical drug to treat a wide range of ailments, including posttraumatic stress disorder, anxiety, depression, asthenia, insomnia, alcoholism, stuttering, and vestibular disorders, among other conditions. In some other parts of the world, phenibut is not approved for clinical use, and is instead sold as a nutritional supplement. It has been reported by some researchers to possess nootropic actions for its ability to improve neurological functions,[medical citation needed] but others have not observed these effects. It is generally accepted that phenibut has anxiolytic effects in both animal models and in humans.
Phenibut is a close structural analogue of GABA, as well as of baclofen (β-(4-chlorophenyl)-GABA), pregabali (β-isobutyl-GABA), and GABOB (β-hydroxy-GABA). Originally thought to act as a selective GABAB receptor agonist, phenibut has since been found to act preferentially as a blocker of α2δ subunit-containing voltage-gated calcium channels, similarly to gabapentin and pregaba. As such, by definition, phenibut is a gabapentinoid.
Basic Info
Chemical Name | 4-Amino-3-phenylbutyric acid hydrochloride |
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Synonyms | phenylgam;PHENIBUT;fenigama;FENIBUT;fenigam;Benzenepropanoic acid, β-(aminomethyl)-;phenigam;pgaba;phenigama;Phenybut;Phenygam;Collapse |
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CAS No. | 1078-21-3 |
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Molecular Formula | C10H14ClNO2 |
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Molecular Weight | 215.67700 |
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PSA | 63.32000 |
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LogP | 2.70590 |
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Properties
Melting Point | 194.0-202.0°C |
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Safety Info
HS Code | 2922499990 |
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Hazard Codes | Xi |
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Detailed Photos
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