2643-78-9 Usage
Description
(S)-2-AMINO-3-PHENYL-BUTYRIC ACID, commonly known as Phenibut, is a synthetic derivative of the neurotransmitter GABA. It is a psychoactive substance that possesses anxiolytic, mood-enhancing, and cognitive-improving properties. As a GABA receptor agonist, it activates these receptors in the brain, which contributes to its therapeutic effects on anxiety and mood regulation.
Uses
Used in Pharmaceutical Industry:
Phenibut is used as a psychoactive drug for its anxiolytic effects, helping to alleviate anxiety and promote relaxation. It is particularly beneficial for individuals suffering from stress, anxiety disorders, and insomnia.
Used in Neurological Applications:
Phenibut is utilized as a nootropic agent to enhance cognitive function and memory. Its ability to improve brain function makes it a potential candidate for the treatment of neurological conditions associated with cognitive decline or memory impairment.
Used in Sports and Performance Enhancement:
Due to its mood-enhancing and relaxing properties, Phenibut is used by athletes and individuals seeking to improve their performance under pressure. It can help reduce pre-competition anxiety and improve focus and mental clarity during high-stress situations.
Used in Research and Development:
Phenibut is employed in scientific research as a GABA receptor agonist to study the effects of GABAergic compounds on the central nervous system. This research can contribute to the development of new therapeutic agents for various neurological and psychiatric disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 2643-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2643-78:
(6*2)+(5*6)+(4*4)+(3*3)+(2*7)+(1*8)=89
89 % 10 = 9
So 2643-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-7(9(11)10(12)13)8-5-3-2-4-6-8/h2-7,9H,11H2,1H3,(H,12,13)/t7?,9-/m0/s1
2643-78-9Relevant articles and documents
Stereoinversion of β- and γ-substituted α-amino acids using a chemo-enzymatic oxidation-reduction procedure
Enright, Alexis,Alexandre, Francois-Rene,Roff, Geoffrey,Fotheringham, Ian G.,Dawson, Michael J.,Turner, Nicholas J.
, p. 2636 - 2637 (2007/10/03)
Both D- and L-β- and γ-substituted α-amino acids can be interconverted to their respective L- and D- diastereoisomers by treatment with an enantioselective amino acid oxidase and a chemical reducing agent.
