4F-Phenibut Free Base

Description

4F-Phenibut Free Base Overview

4F-Phenibut Free Base is a fluorinated analog of phenibut, a compound structurally related to gamma-aminobutyric acid (GABA). The addition of a fluorine atom to the phenibut structure may influence the compound's chemical properties and receptor-binding characteristics.

In laboratory environments, 4F-Phenibut Free Base is utilized as a research compound to investigate mechanisms associated with neurotransmitter systems and central nervous system signaling pathways. Researchers study this compound to better understand how structural modifications may influence receptor interactions and downstream signaling activity.

Chemical and Molecular Properties

PubChem CID	103611
Molecular Formula	C10H12FNO2
Molecular Weight	197.210 g/mol
Synonyms	β-(4-Fluorophenyl)-γ-aminobutyric acid 4-Amino-3-(4-fluorophenyl)butyric acid Benzenepropanoic acid, β-(aminomethyl)-4-fluoro
IUPAC	4-Amino-3-(4-fluorophenyl)butanoic acid
CAS	1858241-03-8
Labeling	Research Use Only (RUO), not for human or animal consumption
Chemical Structure Depiction
Purity	99%
Classification	Research Use Only (RUO)
Storage Temperature	Store at -20°C (-4°F) for long-term stability
Solubility	Water, DMSO (research-grade solvents)
Safety	Handle with gloves, a lab coat, eye protection; use a fume hood if dust/aerosol is possible

Mechanisms of Action

In controlled laboratory investigations, 4F-Phenibut has been studied in experimental models for potential interactions with GABA-related receptor systems involved in inhibitory neurotransmission.

Research models suggest that phenibut and structurally related analogs have been studied for interactions with GABA-B receptor pathways; however, the specific receptor-binding profile of 4F-Phenibut remains under investigation.

Some studies explore its potential interactions with additional neurotransmitter-related pathways; however, these mechanisms are not fully characterized. These pathways have been described in literature in relation to neurological processes such as motivation, reward signaling, and cognitive function.

Further investigation is required to fully characterize the receptor-binding profile and intracellular signaling activity associated with 4F-Phenibut.

Potential Research Applications

Within laboratory settings, 4F-Phenibut is investigated for several areas of neurochemical research, including:

• Examination of GABA receptor-associated signaling pathways
• Evaluation of fluorinated phenibut analogs and their receptor-binding characteristics
• Analysis of neurotransmitter modulation in experimental models
• Investigation of central nervous system signaling mechanisms related to inhibitory neurotransmission
• Comparative studies between phenibut and structurally modified derivatives

These research efforts help scientists better understand how structural changes to GABA-related compounds may influence receptor activity and cellular signaling processes.

Disclaimer

This information is for educational purposes only and not medical advice. Products are for research use only. Research must follow IRB or IACUC guidelines. Verify information independently before purchasing. By ordering, you agree to our Terms and Conditions. If you are not 100% satisfied with the product you received, please contact us at support@staging.purerawz.co

ATTENTION: All our products are for LABORATORY AND RESEARCH PURPOSES ONLY, not for veterinary or human use.

References:

• Irie, T., Yamazaki, D., & Kikura-Hanajiri, R. (2020). F-phenibut (β-(4-Fluorophenyl)-GABA), a potent GABAB receptor agonist, activates an outward-rectifying K+ current and suppresses the generation of action potentials in mouse cerebellar Purkinje cells. European Journal of Pharmacology, 884, 173437. https://doi.org/10.1016/j.ejphar.2020.173437
• Lapin, I. (2001). Phenibut (β-Phenyl-GABA): a tranquilizer and nootropic drug. CNS Drug Reviews, 7(4), 471-481. https://doi.org/10.1111/j.1527-3458.2001.tb00211.x