Abstract

In this study, a novel silver N-heterocyclic carbene (Ag-NHC) complex bearing hydroxyethyl substituent has been synthesized from the hydroxyethyl-substituted benzimidazolium salt and silver oxide by using in-situ deprotonation method. A structure of the Ag-NHC complex was characterized by using UV-Vis, FTIR, 1H-NMR and 13C-NMR spectroscopies and elemental analysis techniques. Also, the crystal structure of the novel complex was determined by single-crystal X-ray diffraction method. In this paper, compound 1 showed excellent inhibitory effects against some metabolic enzymes. This complex had Ki of 1.14 0.26 µM against human carbonic anhydrase I (hCA I), 1.88±0.20 µM against human carbonic anhydrase II (hCA I), and 10.75±2.47 µM against α-glycosidase, respectively. On the other hand, the Ki value was found as 25.32±3.76 µM against acetylcholinesterase (AChE) and 41.31±7.42 µM against butyrylcholinesterase (BChE), respectively. These results showed that the complex had drug potency against some diseases related to using metabolic enzymes.

Highlights

  • A Novel Ag-N-Heterocyclic Carbene ComplexBearing the Hydroxyethyl Ligand: Synthesis, Characterization, Crystal and Spectral Structures and Bioactivity Properties

  • Medical applications of the silver metal were discovered a long time ago [1]

  • Inhibition of this metabolic enzyme acts as a strategy for the duration of senile dementia, Parkinson’s disease, ataxia, Alzheimer’s disease (AD), myasthenia gravis and some disorders of autonomic nervous system functions

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Summary

A Novel Ag-N-Heterocyclic Carbene Complex

Bearing the Hydroxyethyl Ligand: Synthesis, Characterization, Crystal and Spectral Structures and Bioactivity Properties.

Introduction
Materials and Methods
Synthesis of Ag-NHC Complex 1
Biochemical Studies
X-ray Crystallography
44 H 56 Ag 3 Br 3 N 8 O 4
The -CH 3 and -CH 2 proton peaks belonging to the 2ethyl
FTIR Study
TheREVIEW
UV-Vis Study
Description of the Crystal Structure of Ag-NHC Complex 1
Enzyme Inhibition Studies
Conclusions
Full Text
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