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8-Fluoroimidazo[1,2-a]pyridine: synthesis, physicochemical properties and evaluation as a bioisosteric replacement for imidazo[1,2-a]pyrimidine in an allosteric modulator ligand of the GABA A receptor.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2006 Mar 15; Vol. 16 (6), pp. 1518-22. Date of Electronic Publication: 2006 Jan 04. - Publication Year :
- 2006
-
Abstract
- 8-Fluoroimidazo[1,2-a]pyridine has been established as a physicochemical mimic of imidazo[1,2-a]pyrimidine, using both in silico and traditional techniques. Furthermore, a novel synthesis of a 3,7-disubstituted-8-fluoroimidazopyridine 3 has been developed and the utility of the physicochemical mimicry has been demonstrated in an in vitro system. Here, the 8-fluoroimidazopyridine ring contained in ligand 3 acts as a bioisosteric replacement for imidazopyrimidine in the GABA(A) receptor modulator 2.
- Subjects :
- Animals
Fibroblasts cytology
Fibroblasts drug effects
Fibroblasts metabolism
GABA Agonists chemistry
GABA Agonists pharmacology
Humans
Imidazoles chemistry
Imidazoles pharmacology
Ligands
Mice
Molecular Structure
Pyridines chemistry
Pyridines pharmacology
Recombinant Proteins agonists
Structure-Activity Relationship
Allosteric Regulation drug effects
GABA Agonists chemical synthesis
GABA-A Receptor Agonists
Imidazoles chemical synthesis
Pyridines chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 16
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 16386901
- Full Text :
- https://doi.org/10.1016/j.bmcl.2005.12.037