Original articleDevelopment of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors
-
Add time:08/20/2019 Source:sciencedirect.com
A new series of potential GABA uptake inhibitors starting from of 1H-imidazol-4-ylacetic acid with the carboxylic acid side chain originating from different positions and varying in length have been synthesized and tested for the inhibitory potency at the four GABA uptake transporters mGAT1–4 stably expressed in HEK cells. Further two bicyclic compounds with a rigidified carboxylic acid side chain were included in this study. The results of the biological tests indicated that most ω-imidazole alkanoic and alkenoic acid derivatives exhibit the highest potencies as GABA uptake inhibitors at mGAT3.
We also recommend Trading Suppliers and Manufacturers of 1-(Triphenylmethyl)imidazole (cas 15469-97-3). Pls Click Website Link as below: cas 15469-97-3 suppliers
Prev:Research paperAssembly of a mononuclear ferrous site using a bulky aldehyde-imidazole ligand
Next:Novel metal chelating molecules with anticancer activity. Striking effect of the imidazole substitution of the histidine–pyridine–histidine system) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Chapter 9 Imidazoles08/23/2019
- Research paperSynthesis and biological evaluation of a series of N-alkylated imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors08/22/2019
- Novel metal chelating molecules with anticancer activity. Striking effect of the imidazole substitution of the histidine–pyridine–histidine system08/21/2019
- Research paperAssembly of a mononuclear ferrous site using a bulky aldehyde-imidazole ligand08/19/2019


