Publications by authors named "Ch Sarala Devi"

The molecular and QSAR (Quantitative Structure-Activity Relationship) properties of title compound 2-((6-Methoxybenzo[d]thiazol-2-ylimino)methyl)-6-ethoxyphenol (HL) were evaluated employing HyperChem 7.5 tools. The interaction of the complexes of HL with calf thymus DNA (CT-DNA) was investigated by absorption titrations, Fluorescence quenching and viscosity measurements.

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Three mononuclear, mixed ligand ternary Cu(II) complexes of 3-((Z)-1-(2-hydroxyphenylimino)ethyl)-4-hydroxy-6-methyl-2H-pyran-2-one (HEHMP) viz; [Cu-(Phen) (HEHMP)] (), [Cu-(Bpy)(HEHMP)] () and [Cu-Bpy(NCS)(HEHMP)] () were synthesized and characterized by data obtained from various spectral techniques. The binding affinities of these complexes with calf thymus DNA (CT-DNA) and bovine serum albumin (BSA) protein were explored by absorption and fluorescence quenching titrations. The results indicated strong affinity of the title compounds to bind with both CT-DNA and BSA.

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Some novel transition metal [Cu (II), Ni (II) and Co (II)] complexes of nalidixic acid hydrazone have been prepared and characterized by employing spectro-analytical techniques viz: elemental analysis, H-NMR, Mass, UV-Vis, IR, TGA-DTA, SEM-EDX, ESR and Spectrophotometry studies. The HyperChem 7.5 software was used for geometry optimization of title compound in its molecular and ionic forms.

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The compound N-(2-hydroxybenzylidene)-1-ethyl-1, 4-dihydro-7-methyl-4-oxo-1, 8 naphthyridine-3-carbohydrazide (LH) and its Cu (II), Co (II) and Zn (II) complexes were synthesized and characterized. The absorption spectral titrations and competitive DNA binding studies depicted those complexes of title compound bind to CT-DNA through intercalation. Interestingly [Cu (II)-(L2)] showed relatively high binding constant value (6.

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Article Synopsis
  • The study focuses on developing and analyzing metal complexes (Cu (II), Cd (II), Ce (IV), and Zr (IV)) using a specific imine derivative, including their DNA interaction, photo-cleavage, and antioxidant properties.
  • Characterization techniques such as EDX, IR, and NMR were used to confirm the synthesis of these complexes, while spectrophotometric methods assessed their reactivity and interactions with DNA, revealing a tendency to intercalate.
  • The results indicated that these metal complexes exhibit significant antibacterial activity and dose-dependent cytotoxicity in cell lines, suggesting potential for new therapeutic drug development, bolstered by molecular modeling and docking studies to understand receptor interactions.
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