Pyridine substituted BODIPYs: synthesis, characterization and cholinesterease, alpha-glucosidase inhibitory, DNA hydrolytic cleavage effects


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BARUT B. , Bas H., BIYIKLIOĞLU Z.

TURKISH JOURNAL OF CHEMISTRY, vol.45, no.5, pp.1567-1580, 2021 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Article
  • Volume: 45 Issue: 5
  • Publication Date: 2021
  • Doi Number: 10.3906/kim-2105-59
  • Title of Journal : TURKISH JOURNAL OF CHEMISTRY
  • Page Numbers: pp.1567-1580
  • Keywords: Synthesis, BODIPY, anticholinesterase, DNA hydrolytic cleavage, COMPLEXES, LIGANDS

Abstract

In this study, the synthesis of new monostyryl (BDPY-2) and distyryl BODIPY dyes (BDPY-4, BDPY-5) containing pyridine groups has been reported for the first time. The acetylcholinesterase from Electrophorus electricus (AChE), butyrylcholinesterase from equine scrum (BuChE), alpha-glucosidase from Saccharomyces cerevisiae and DNA hydrolytic cleavage actions of BDPY-2, BDPY-4, BDPY-5 were investigated using various techniques. The results indicated that the compounds had varying inhibition properties against AChE, BuChE, and alpha-glucosidase. BDPY-4 was the most potent compound on AChE with IC50 of 54.78 +/- 4.51 mu M, and Lineweaver-Burk plots indicated that the compound is bound to a site other than the active site as a noncompetitive inhibitor. 1 he compound-protein binding experiment showed that BDPY-4 changed the microenvironment around AChE. On the other hand, the compounds showed lower alpha-glucosidase inhibition than the positive control. The DNA hydrolytic cleavage effects were not observed on supercoiled plasmid DNA in the presence of the compounds as compared to negative controls. These findings suggested that BDPY-4 might be a promising compound to treat Alzheimer's diseases.