2021
DOI: 10.1080/07391102.2020.1858163
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Synthesis, characterization, molecular docking and in vitro screening of new metal complexes with coumarin Schiff base as anticholine esterase and antipancreatic cholesterol esterase agents

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Cited by 15 publications
(7 citation statements)
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“…Sahin and coworkers synthesized a Schiff base-coumarin hybrid and coordinated it with Pd(II) or Pt (II) (compound 65) ( Şahin et al, 2022 ). The novel compounds were tested for inhibitory activity toward AChE, butyrylcholinesterase (BChE), and pancreatic cholesterol esterase (CEase).…”
Section: Coumarin Complexes As Enzyme Inhibitors and Antihaemolytic A...mentioning
confidence: 99%
“…Sahin and coworkers synthesized a Schiff base-coumarin hybrid and coordinated it with Pd(II) or Pt (II) (compound 65) ( Şahin et al, 2022 ). The novel compounds were tested for inhibitory activity toward AChE, butyrylcholinesterase (BChE), and pancreatic cholesterol esterase (CEase).…”
Section: Coumarin Complexes As Enzyme Inhibitors and Antihaemolytic A...mentioning
confidence: 99%
“…The 100 ml of pure water, the 80 μL of 100 mM Tris-SO4 buffer (pH: 8.0), the 80 μl of 3 mM 4-nitrophenyl acetate, and 20 μL enzyme were added to the reaction mix for human CA isoenzymes (hCAI and hCAII). [27] For porcine PCE activity assay, the reaction mixture was created by adding 80 μl of 100 mM phosphate buffer (pH:7) containing 100 mM NaCl, 100 μl of 12 mM NAT, 20 μl of 20 mM p-nitrophenyl butyrate at assay buffer, 80 μL of pure water and 10 μL enzyme [28,29] For inhibition studies, the compound was dissolved as 1 mg/ml at DMSO, and then diluted 10 times with distilled water to use as a stock solution. Enzyme activities were assayed at the different inhibitory concentrations by reducing the amount of water as much as the inhibitor volume.…”
Section: Enzyme Studiesmentioning
confidence: 99%
“…Şahin et al demonstrated the inhibitory potency of palladium (II) and platinum (II) complexes of coumarin-based ligand - 3-{2-[(3-( tert -butyl)-2-hydroxybenzylidene)amino]thiazol-4-yl}-2 H -chromen-2-one 54 and 55 ( Table 1 ) against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and pancreatic cholesterol esterase (cease) ( Şahin et al, 2020 ). The inhibitory properties against AChE, BChE, and cease of synthesized complexes were determined by a standard procedure involving the spectrophotometric measurements according to Elman or Pietsch and Gütschow methods.…”
Section: Enzyme Inhibiting Complexesmentioning
confidence: 99%