Agonist responses of (R)- and (S)-3-fluoro-γ-aminobutyric acids suggest an enantiomeric fold for GABA binding to GABAC receptors-Reference-Cited by-同舟云学术

Agonist responses of (R)- and (S)-3-fluoro-γ-aminobutyric acids suggest an enantiomeric fold for GABA binding to GABAC receptors

Published:2011 Issue:28 Volume:47 Page:7956
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yamamoto Izumi,Deniau Gildas P.,Gavande Navnath,Chebib Mary,Johnston Graham A. R.,O'Hagan David

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2011/CC/C1CC12141C

Reference29 articles.

1. Distribution of GABAA and GABAB receptors in mammalian brain: Potential targets for drug development

2. GABA-Activated Ligand Gated Ion Channels: Medicinal Chemistry and Molecular Biology

3. An Updated Unified Pharmacophore Model of the Benzodiazepine Binding Site on γ-Aminobutyric Acida Receptors: Correlation with Comparative Models

4. Medicinal Chemistry and Molecular Pharmacology of GABA-C Receptors

5. Medicinal chemistry of ρ GABAC receptors

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis and physicochemical evaluation of tetrafluorinated GABA analogue;Journal of Fluorine Chemistry;2024-07

2. Zn/F carbenoids: preparation, structures, stability, and application to nucleophilic monofluoroalkylation;Organic Chemistry Frontiers;2024

3. Direct syntheses of stereoisomers of 3-fluoro GABA and β-fluoroamine analogues of the calcium receptor (CaR) agonists, cinacalcet, tecalcet, fendiline and NPS R-467;Medicinal Chemistry Research;2023-07

4. Direct syntheses of stereoisomers of 3-fluoro GABA and β-fluoroamine analogues of the calcium receptor (CaR) agonists, cinacalcet, tecalcet, fendilines and NPS R-467;2023-05-19

5. Highly Diastereoselective Construction of Carbon– Heteroatom Quaternary Stereogenic Centers in the Synthesis of Analogs of Bioactive Compounds: From Monofluorinated Epoxyalkylphosphonates to α-Fluoro-, β-, or γ-Amino Alcohol Derivatives of Alkylphosphonates;Frontiers in Chemistry;2021-06-02