| Literature DB >> 31015178 |
Hayriye Genç Bilgiçli1, Ali Kestane2, Parham Taslimi3, Oguz Karabay4, Arlinda Bytyqi-Damoni5, Mustafa Zengin2, İlhami Gulçin6.
Abstract
Five oxypropanol amine derivatives that four of them are novel have been synthesized with high yields and practical methods. in vitro antibacterial susceptibility of Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli and Staphylococcus aureus strains to synthesized substances were evaluated with agar well-diffusion method by comparison with commercially available drugs. Most of the bacteria were multidrug resistant. It was concluded that these compounds are much more effective than reference drugs. These eugenol bearing oxypropanolamine derivatives were also effective inhibitors against α-glycosidase, cytosolic carbonic anhydrase I and II isoforms (hCA I and II), and acetylcholinesterase (AChE) enzymes with Ki values in the range of 0.80 ± 0.24-3.52 ± 1.01 µM for hCA I, 1.08 ± 0.15-3.64 ± 0.92 µM for hCA II, 5.18 ± 0.84-12.46 ± 2.08 µM for α-glycosidase, and 11.33 ± 2.83-32.81 ± 9.73 µM for AChE, respectively.Entities:
Keywords: Acetylcholinesterase; Antibacterial effects; Carbonic anhydrase; Enzyme inhibition; Eugenol; α-glycosidase
Year: 2019 PMID: 31015178 DOI: 10.1016/j.bioorg.2019.102931
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275