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Article 2024 · 12 citations

Synthesis, characterization, crystal structure, biological activities, and molecular docking study of the (NHC)Pd(II)(Morp) (NHC:<i> N</i>-heterocyclic carbene, Morp: Morpholine) complexes

Aktas, Aydin, Taslimi, Parham, Bal, Selma, Celepci, Duygu Barut, Gok, Yetkin, Taskin-Tok, Tugba, Aygun, Muhittin, Gulcin, Lhami

Abstract

In this paper, a new palladium -based (NHC)Pd(II)(Morp) complexes (NHC: N -heterocyclic carbene, Morp: morpholine) were prepared. The NHC ligand in these complexes bears the 2-chloro-4-fluorobenzyl group. All complexes were fully characterized by 1 H, 13 C NMR, FTIR spectroscopic and elemental analysis methods. The crystal structure of complex 1f has been determined by using single-crystal X-ray diffraction. Furthermore, all complexes were investigated for their ability to inhibit enzymes. All complexes exhibited highly potent inhibition effects on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes (K i values are in the range of 97.84 +/- 8.97 to 132.28 +/- 11.63 mu M and 18.24 +/- 2.08 to 39.08 +/- 5.28 mu M for AChE and BChE, respectively). Designing of reported complexes is impacted by molecular docking study, because with molecular docking study, it will lead to future researches by illuminating the interaction mechanism of complexes 1a , 1b , 1c and 1f with potential activity against target AChE and BChE enzymes at molecuar level.

Keywords
Acetylcolineesterase Butylcolineesterace Crystal structure Molecular docking N -heterocyclic carbene MEDICINAL CHEMISTRY VALIDATION FLUORINE
WoS Categories
Chemistry, Inorganic & Nuclear Crystallography
Sustainable Development Goals
Citation
Journal
POLYHEDRON
Year
2024
Volume
257
ISSN
0277-5387
eISSN
1873-3719
DOI
10.1016/j.poly.2024.117016
WoS UID
WOS:001239162700001
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