Article detail · 2018 · article
Synthesis and characterization of novel substituted thiophene derivatives and discovery of their carbonic anhydrase and acetylcholinesterase inhibition effects
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- YÖKSİSYÖKSİS article record
- YÖKSİS venueJOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY
- Catalog match (ISSN)Journal of Biochemical and Molecular Toxicology
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Abstract
Abstract Novel substituted thiophene derivatives (1, 2a‐e, 3, and 4) were synthesized and their structures were characterized by infrared radiation, nuclear magnetic resonance, and mass analysis. These novel substituted thiophene derivatives were effective inhibitor compounds of the carbonic anhydrase I and II isozymes (hCA I and II), and acetylcholinesterase (AChE) enzyme with K i values in the range of 447.28 to 1004.65 nM for hCA I, 309.44 to 935.93 nM for hCA II, and 0.28 to 4.01 nM for AChE, respectively. Novel substituted thiophene derivatives can be good candidate drugs for the treatment of some diseases like neurological disorders, epilepsy, glaucoma, gastric and duodenal ulcers, mountain sickness, or osteoporosis as carbonic anhydrase isozymes inhibitors, and for the treatment of Alzheimer’s and Parkinson’s diseases as acetylcholinesterase inhibitors.
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39citationsOpenAlex · cited_by_count (cache / database)
62 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
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