Recent developments on the potential biological applications of transition metal complexes of thiosemicarbazone derivatives
V Singh, VNV Palakkeezhillam, V Manakkadan… - Polyhedron, 2023 - Elsevier
This review talks about the synthesis, and coordination chemistry of thiosemicarbazone and
its bonding with transition metals like copper, nickel, zinc, palladium, and ruthenium and …
its bonding with transition metals like copper, nickel, zinc, palladium, and ruthenium and …
[HTML][HTML] Photocatalytic degradation of Rhodamine B (RhB) dye in waste water and enzymatic inhibition study using cauliflower shaped ZnO nanoparticles synthesized …
Abstract The ZnO nanoparticles (NPs) are considered to be one of the inexpensive and very
important bioactive materials widely used in drug delivery, as a photo-catalyst material …
important bioactive materials widely used in drug delivery, as a photo-catalyst material …
Novel 2-aminopyridine liganded Pd (II) N-heterocyclic carbene complexes: Synthesis, characterization, crystal structure and bioactivity properties
In this work, the synthesis, crystal structure, characterization, and enzyme inhibition effects of
the novel a series of 2-aminopyridine liganded Pd (II) N-heterocyclic carbene (NHC) …
the novel a series of 2-aminopyridine liganded Pd (II) N-heterocyclic carbene (NHC) …
Cytotoxic effect, spectroscopy, DFT, enzyme inhibition, and moleculer docking studies of some novel mesitylaminopropanols: Antidiabetic and anticholinergics and …
Abstract β-Amino alcohols (2–4) used in this study were re-synthesized in accordance with
our previous study. All compounds were characterized by the combination of NMR, UV–Vis …
our previous study. All compounds were characterized by the combination of NMR, UV–Vis …
Probing 4-(diethylamino)-salicylaldehyde-based thiosemicarbazones as multi-target directed ligands against cholinesterases, carbonic anhydrases and α-glycosidase …
With the fading of 'one drug-one target'approach, Multi-Target-Directed Ligands (MTDL) has
become a central idea in modern Medicinal Chemistry. The present study aimed to design …
become a central idea in modern Medicinal Chemistry. The present study aimed to design …
Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3, 5‐dimethoxy benzaldehyde …
New Schiff base‐bearing thiosemicarbazones (1–13) were obtained from 4‐hydroxy‐3, 5‐
dimethoxy benzaldehyde and various isocyanates. The structures of the synthesized …
dimethoxy benzaldehyde and various isocyanates. The structures of the synthesized …
Synthesis, characterization, biological evaluation, and in silico studies of novel 1, 3‐diaryltriazene‐substituted sulfathiazole derivatives
In the present study, a series of eleven novel 1, 3‐diaryltriazene‐substituted sulfathiazole
moieties (ST1–11) was synthesized by the reaction of diazonium salt of sulfathiazole with …
moieties (ST1–11) was synthesized by the reaction of diazonium salt of sulfathiazole with …
Design, synthesis, characterization, enzymatic inhibition evaluations, and docking study of novel quinazolinone derivatives
K Pedrood, M Sherafati… - International Journal of …, 2021 - Elsevier
In this study, novel quinazolinone derivatives 7a-n were synthesized and evaluated against
metabolic enzymes including α-glycosidase, acetylcholinesterase, butyrylcholinesterase …
metabolic enzymes including α-glycosidase, acetylcholinesterase, butyrylcholinesterase …
Synthesis, biological activity and docking calculations of bis-naphthoquinone derivatives from Lawsone
Some metabolic enzyme inhibitors can be used as Multi-target-Directed-Ligands (MTDL) in
Medicinal chemistry therefore, synthesis and determination of alternative inhibitors are …
Medicinal chemistry therefore, synthesis and determination of alternative inhibitors are …
Biologically active phthalocyanine metal complexes: Preparation, evaluation of α‐glycosidase and anticholinesterase enzyme inhibition activities, and molecular …
In this study, preparation, as well as investigation of α‐glycosidase and cholinesterase
(ChE) enzyme inhibition activities of furan‐2‐ylmethoxy‐substituted compounds 1–7, are …
(ChE) enzyme inhibition activities of furan‐2‐ylmethoxy‐substituted compounds 1–7, are …