GABA is the endogenous GABAR agonist, muscimol a classical... | Download Scientific Diagram
GABA analogue - Wikipedia
WO2015091463A1 - Gamma-aminobutyric acid (gaba) analogues for the treatment of pain and other disorders - Google Patents
Access to Chiral GABA Analogues Bearing a Trifluoromethylated All-Carbon Quaternary Stereogenic Center through Water-Promoted Organocatalytic Michael Reactions | Organic Letters
Stereodivergent synthesis of cyclic γ-aminobutyric acid – GABA analogues - ScienceDirect
General structure of GABA analogues (SKP 1-16) | Download Scientific Diagram
Structures of GABA, 4-PIOL, and the cyclopentane GABA analogues | Download Scientific Diagram
Conformationally restricted GABA analogs: from rigid carbocycles to cage hydrocarbons | Future Medicinal Chemistry
GABA analogues - Structure, Properties, uses, Synthesis, Assay, Storage, Dosage forms, Dose | Synthesis and Drug Profile | Anticonvulsants
Molecules | Free Full-Text | Novel-Substituted Heterocyclic GABA Analogues. Enzymatic Activity against the GABA-AT Enzyme from Pseudomonas fluorescens and In Silico Molecular Modeling
![Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c01346/asset/images/large/ol2c01346_0001.jpeg "Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters")
Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters
Progabide is an analogue and prodrug of g aminobutyric acid used in the treatment of epilepsy.
Gaba Supplements: Glorious, Gimmicky or Just Garbage? | Office for Science and Society - McGill University
Scheme 1 Synthesis of fluorinated GABA analogues 3 and 4. Reagents and... | Download Scientific Diagram
An enigmatic role of tonic inhibition in gabapentin therapy - eBioMedicine
Antagonistic effect of dopamine structural analogues on human GABAρ1 receptor | Scientific Reports
File:GABA analogues.jpg - Wikimedia Commons
Life | Free Full-Text | Pharmacological Effect of GABA Analogues on GABA-ϱ2 Receptors and Their Subtype Selectivity
GABA analogues screened against OAT. | Download Scientific Diagram
Molecules | Free Full-Text | QSAR and Molecular Docking Studies of the Inhibitory Activity of Novel Heterocyclic GABA Analogues over GABA-AT
Gaba receptors & drugs acting on them
Synthesis and resolution of 2-methyl analogues of GABA - ScienceDirect
![Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c01346/asset/images/large/ol2c01346_0008.jpeg "Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters")
Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters
Gaba analogue hi-res stock photography and images - Alamy
Figure 1 from MOLECULAR INTERACTIONS OF GABA ANALOGUES AGAINST THE α+β-INTERFACE OF GABAA RECEPTOR: DOCKING AND MOLECULAR DYNAMICS STUDIES | Semantic Scholar
GABA analogues - Structure, Properties, uses, Synthesis, Assay, Storage, Dosage forms, Dose | Synthesis and Drug Profile | Anticonvulsants
Exploring the molecular determinants for subtype-selectivity of 2-amino-1,4,5,6-tetrahydropyrimidine-5-carboxylic acid analogs as betaine/ GABA transporter 1 (BGT1) substrate-inhibitors | Scientific Reports
![A conformationally restricted GABA analogue based on octahydro-1H-cyclopenta[b]pyridine scaffold | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00726-018-2660-1/MediaObjects/726_2018_2660_Fig2_HTML.png "A conformationally restricted GABA analogue based on octahydro-1H-cyclopenta[b]pyridine scaffold | SpringerLink")
A conformationally restricted GABA analogue based on octahydro-1H-cyclopenta[b]pyridine scaffold | SpringerLink
![Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c01346/asset/images/large/ol2c01346_0005.jpeg "Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors | Organic Letters")