Ahmet Yaşar's research while affiliated with Gazi University and other places

What is this page?


This page lists the scientific contributions of an author, who either does not have a ResearchGate profile, or has not yet added these contributions to their profile.

It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.

If you're a ResearchGate member, you can follow this page to keep up with this author's work.

If you are this author, and you don't want us to display this page anymore, please let us know.

Publications (2)


Synthesis of novel Schiff base derivatives of Tacrine and investigation of their acetylcholinesterase inhibition potency
  • Article

June 2019

·

41 Reads

Macedonian Journal of Chemistry and Chemical Engineering

Elif Aynacı Koyuncu

·

Ahmet Yaşar

·

·

Share

Fig. 1. (a) Tacrine. (b) Tacrine with protonated acridine nitrogen [12]. (c) Donepezil. (d) Physostigmine.
Fig. 3. AChE activity assay by Ellman method
Synthesis of novel Schiff base derivatives of tacrine and investigation of their acetylcholinesterase inhibition potency
  • Article
  • Full-text available

May 2019

·

2,278 Reads

·

5 Citations

Macedonian Journal of Chemistry and Chemical Engineering

Investigation of acetylcholinesterase (AChE) inhibition potency of some new Schiff base derivatives of tacrine (9-amino-1,2,3,4-tetrahydroacridine) was reported in this paper. Novel Schiff base derivatives of tacrine (3a–g) have been synthesized, and they have been characterized by several methods (FT-IR, 1H-NMR, 13C-NMR, etc.). Then, inhibition effects on AChE by the synthesized compounds have been investigated by the spectrophotometric Ellman method. IC50, Ki, KM and Vmax values and inhibition types have been determined. It was seen that all compounds had the property of a water-soluble reversible AChE inhibitor. Structure 3a was found to be the most potent inhibitor, with the IC50 value of 22.1 ± 1.11 nM (tacrine's IC50 value was calculated as 34.1 nM).

Download

Citations (1)


... inhibition of the enzyme. Certain derivatives of Schiff bases showed pronounced activity as AChE inhibitors [51] as well as butyrylcholinesterase (BuChE) and monoamine oxidase (MAO) [52,53]. Obtained results are in correlation with the nematicidal activity assays where the same compound displayed the highest activity. ...

Reference:

Effects of Coumarinyl Schiff Bases against Phytopathogenic Fungi, the Soil-Beneficial Bacteria and Entomopathogenic Nematodes: Deeper Insight into the Mechanism of Action
Synthesis of novel Schiff base derivatives of tacrine and investigation of their acetylcholinesterase inhibition potency

Macedonian Journal of Chemistry and Chemical Engineering