Abstract
Gamma-aminobutyric acid (GABA) plays a pivotal role in neuronal regulation within the
Brain. This study aims to explore potential interactions between synthesized GABA derivatives and
GATI through molecular docking simulations. Initially, GABA's historical significance and
Therapeutic applications are outlined. The mechanism of action of GABAergic drugs and the role of
GATI are elucidated. Subsequently, using ADME procedures and molecular docking protocols, the
Physicochemical properties of synthesized compounds and their binding affinities to GATI are
Investigated. Results reveal high gastrointestinal absorption and varying blood-brain barrier
Permeability among the compounds. Docking studies show promising interactions, with compound
G8 exhibiting notable affinity attributed possibly to hydrogen bond formations. This research offers
Insights into potential drug development targeting GATI for modulating GABAergic signaling.