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Integrative approach for designing novel triazole derivatives as α-glucosidase inhibitors: QSAR, molecular docking, ADMET, and molecular dynamics investigations
In response to the increasing prevalence of diabetes mellitus and the limitations associated
with the current treatments, there is a growing need to develop novel medications for this …
with the current treatments, there is a growing need to develop novel medications for this …
Sulfamethoxazole-derived Schiff bases: synthesis, characterization, biological activities, molecular docking, DFT, and ADME studies
Herein, we reported the synthesis of sulfamethoxazole-derived Schiff bases (SBs) using
aromatic aldehydes for in-vitro biological applications (antimicrobial, antioxidant …
aromatic aldehydes for in-vitro biological applications (antimicrobial, antioxidant …
Synthesis and Therapeutic Potential of selected Schiff Bases: In vitro Antibacterial, Antioxidant, Antidiabetic, and Computational Studies
In this study, three Schiff base compounds,(E)‐N‐(4‐bromophenyl)‐1‐(2‐nitrophenyl)
methanimine (L1),(E)‐2‐((mesitylimino) methyl) phenol (L2), and (E)‐N‐(4‐bromophenyl)‐1 …
methanimine (L1),(E)‐2‐((mesitylimino) methyl) phenol (L2), and (E)‐N‐(4‐bromophenyl)‐1 …
An experimental and theoretical study of coinage bond interaction in a copper (II)/potassium (I) Schiff base complex
Abstract A copper (II)/potassium (I) Schiff base polymeric complex has been synthesized and
characterized. Salen-type N 2 O 2 O 2′ donor compartmental Schiff base ligand has been …
characterized. Salen-type N 2 O 2 O 2′ donor compartmental Schiff base ligand has been …
Antioxidant Activity and DFT Calculations of Metal Complexes Derived from a Schiff Base Ligand: Synthesis, Characterization, and Biological Evaluation
Metal complexes derived from Schiff bases are known to have a wide range of applications,
spanning the areas of material and medicinal sciences. Herein, a Schiff base ligand,(Z)‐2 …
spanning the areas of material and medicinal sciences. Herein, a Schiff base ligand,(Z)‐2 …
Biological evaluation of a novel Schiff base ligand as an antioxidant agent: Synthesis, characterization and DFT computations of its Ni (II) and Cu (II) complexes
By condensation reaction in methanolic medium, a novel ligand using methoxy substituted
amine and 5-bromosalicylaldehydic was synthesized. Then, its Cu-and Ni-complexes were …
amine and 5-bromosalicylaldehydic was synthesized. Then, its Cu-and Ni-complexes were …
[HTML][HTML] Copper (II) Complexes with 1-(Isoquinolin-3-yl) heteroalkyl-2-ones: Synthesis, Structure and Evaluation of Anticancer, Antimicrobial and Antioxidant Potential
Four copper (II) complexes, C1–4, derived from 1-(isoquinolin-3-yl) heteroalkyl-2-one
ligands L1–4 were synthesized and characterized using an elemental analysis, IR …
ligands L1–4 were synthesized and characterized using an elemental analysis, IR …
Sulfaquinoxaline-derived Schiff bases: Synthesis, characterization, biological profiling, and computational modeling
Here, six sulfaquinoxaline Schiff bases were synthesized, and various analytical techniques
such as FTIR, 1 HNMR, and 13 CNMR were employed for the characterization. Additionally …
such as FTIR, 1 HNMR, and 13 CNMR were employed for the characterization. Additionally …
1, 2, 3-Triazole based xanthene and acridine linkers as potential α-glucosidase and α-amylase inhibitors: Design, green synthesis, kinetics, and in silico studies
In an ongoing endeavor to discover new α-glucosidase as well as α-amylase inhibitors for
the treatment of type 2 diabetes mellitus (T2DM), herein we introduced the synthesis of …
the treatment of type 2 diabetes mellitus (T2DM), herein we introduced the synthesis of …
Thiophene‐2‐ethylamine Based Schiff Base Ligands and Their Co (III), Ni (II), and Cu (II) Metal Complexes: Antimicrobial and Antidiabetic Activities
Thiophene‐2‐ethylamine based Schiff base ligands, namely 2‐((E)‐(2‐(thiophen‐2‐yl)
ethylimino) methyl) phenol (L1H), 2‐((E)‐(2‐(thiophen‐2‐yl) ethylimino) methyl)‐4 …
ethylimino) methyl) phenol (L1H), 2‐((E)‐(2‐(thiophen‐2‐yl) ethylimino) methyl)‐4 …