Tuning Cobalt(III) Schiff Base Complexes as Activated Protein Inhibitors (original) (raw)

Water-soluble Cobalt(II) & Cobalt(III) complexes supported by new triazine Schiff base ligands: Synthesis, structure and biological evaluation

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Light-Activated Protein Inhibition through Photoinduced Electron Transfer of a Ruthenium(II)-Cobalt(III) Bimetallic Complex

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Binding interactions of mixed ligand copper(II) amino acid Schiff base complexes with biological targets: Spectroscopic evaluation and molecular docking

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Synthesis, structural investigation and biological application of new mono- and binuclear cobalt (II) mixed-ligand complexes containing 1,10-phenanthroline, acetamide and ethylenediamine

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Synthesis and characterization of cationic bis-aziridine cobalt (III) complexes containing schiff base ligands

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Synthesis, characterization, electrochemical and spectroscopic investigation of cobalt(III) Schiff base complexes with axial amine ligands: The layered crystal structure of [CoIII(salophen)(4-picoline)2]ClO4 · CH2Cl2

Behrouz Shaabani, Ali Khandar

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Co(II) and Cd(II) Complexes Derived from Heterocyclic Schiff-Bases: Synthesis, Structural Characterisation, and Biological Activity

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The Scientific World Journal, 2013

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Synthesis, spectroscopic characterization, thermal studies, and molecular docking of novel Cr(III), Fe(III), and Co(II) complexes based on Schiff base: In vitro antibacterial and antitumor activities

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IJERT-Ultravoilet and Vibrational Spectral Sudies on Biologically Active Complexes of Cobalt -Ii with Benzimidazole Compound

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International Journal of Engineering Research and Technology (IJERT), 2020

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Photoinduced Electron Transfer from PbS Quantum Dots to Cobalt(III) Schiff Base Complexes: Light Activation of a Protein Inhibitor

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Synthesis, characterization and biological activities of mononuclear Co(III) complexes as potential bioreductively activated prodrugs

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Six-coordinate oxime-imine cobalt(III) complexes with amino acid co-ligands; synthesis and characterisation

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A Route to Bis(benzimidazole) Ligands with Built-In Asymmetry: Potential Models of Protein Binding Sites Having Histidines of Different Basicity

Mark Elsegood

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Synthetic routes to mixed-ligand cobalt(III) dithiocarbamato complexes containing imidazole, amine and pyridine donors and the X-ray crystal structure of a cobalt(III) bis(dithiocarbamato) histamine complex

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Dinuclear cobalt(II) complexes of Schiff-base compartmental ligands: Syntheses, crystal structure and bio-relevant catalytic activities

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Synthesis, characterization, spectroscopic and crystallographic investigation of Cobalt(III) schiff base complex with two perpendicular diamine coumarin ligands

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IJERT-Ultraviolet and Vibrational Spectral Studies on Biologically Active Complexes of Cobalt -Ii with Benzimidazole Compound

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Synthesis, structure and supramolecular features of cobalt(III) and cobalt(II) complexes, CoHxLy (x=y=3, 2, 1.50, 1.45, 1 and 0 and x=3, y=2) of a triprotic imidazole containing Schiff base ligand. Effect of protonation state on supramolecular structure

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Coordination induced 2-(2′-hydroxyphenyl) imidazolidine ring hydrolysis of dinucleating amine–imine–phenol ligands: X-ray structures of hardness-matched mononuclear cobalt(III) complexes as end products having isomeric N4O2 coordination spheres

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Synthesis, structure, and ion-binding studies of cobalt(II) complexes with aza-crown substituted salicylaldimine Schiff base ligand

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Practical and computational studies on novel Schiff base complexes derived from green synthesis approach: Conductometry as well as in-vitro screening supported by in-silico study

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Synthesis, crystal structure and antibacterial activity of azido complexes of cobalt(III) containing heteroaromatic Schiff bases

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Modulation of Amyloid-β Aggregation by Histidine-Coordinating Cobalt(III) Schiff Base Complexes

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Novel Benzimidazole Derived Imine Ligand and Its Co(III) and Cu(II) Complexes as Anticancer Agents: Chemical Synthesis, DFT Studies, In Vitro and In Vivo Biological Investigations

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Doubly end-on azido bridged mixed-valence cobalt trinuclear complex: Spectral study, VTM, inhibitory effect and antimycobacterial activity on human carcinoma and tuberculosis cells

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