Literature DB >> 16781158

Synthesis, characterization, and DNA-binding properties of the Ln(III) complexes with 6-hydroxy chromone-3-carbaldehyde-(2'-hydroxy) benzoyl hydrazone.

Bao-dui Wang1, Zheng-Yin Yang, Tian-rong Li.   

Abstract

A new ligand, 6-hydroxy chromone-3-carbaldehyde-(2'-hydroxy) benzoyl hydrazone (L), was prepared by condensation of 6-hydroxy-3-carbaldehyde chromone (CDC) with 2-hydroxy benzoyl hydrazine. Its four rare earth complexes have been synthesized and characterized on the basis of elemental analyses, molar conductivities, mass spectra, 1H NMR, thermogravimetry/differential thermal analysis (TG-DTA), UV-vis spectra, fluorescence spectra, and IR spectra. The general formula of the complexes is [LnL2.(NO3)2].NO3 [Ln=La(1), Sm(2), Dy(3), Eu(4)]. Spectrometric titration, ethidium bromide displacement experiments, and viscosity measurements indicate that Eu(III) complex and ligand, especially the Eu(III) complex, strongly bind with calf-thymus DNA, presumably via an intercalation mechanism. The intrinsic binding constants of Eu(III) complex and ligand with DNA were 3.55 x 10(6) and 1.33 x 10(6)M(-1) through fluorescence titration data, respectively. In addition, the suppression ratio for O2-* and OH* of the ligand and its complexes was studied by spectrophotometric methods. The experimental results show that La (1), Sm (2), and Eu (4) complexes are better effective inhibitor for OH* than that of mannitol. It indicates that the complexes have the activity to suppress O2-* and OH* and exhibit more effective antioxidants than ligand alone.

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Year:  2006        PMID: 16781158     DOI: 10.1016/j.bmc.2006.05.015

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  9 in total

Review 1.  Spirocyclic derivatives as antioxidants: a review.

Authors:  Karen Acosta-Quiroga; Cristian Rojas-Peña; Luz Stella Nerio; Margarita Gutiérrez; Efraín Polo-Cuadrado
Journal:  RSC Adv       Date:  2021-06-21       Impact factor: 4.036

2.  Synthesis, characterization, DNA-binding properties of the Ln(III) complexes with 6-hydroxy chromone-3-carbaldehyde-(4'-hydroxy) benzoyl hydrazone.

Authors:  Bao-Dui Wang; Zheng-Yin Yang
Journal:  J Fluoresc       Date:  2007-12-12       Impact factor: 2.217

3.  Synthesis, characterization and DNA-binding properties of Ln(III) complexes with 6-ethoxy chromone-3-carbaldehyde benzoyl hydrazone.

Authors:  Ju Wang; Zheng-Yin Yang; Bao-Dui Wang; Xu-Yang Yi; Yong-Chun Liu
Journal:  J Fluoresc       Date:  2009-04-16       Impact factor: 2.217

4.  Fluorescence and biological evaluation of the La(III) and Eu(III) complexes with 7-methoxychromone-3-carbaldehyde benzoyl hydrazone Schiff base.

Authors:  Dong-dong Qin; Gao-fei Qi; Zheng-yin Yang; Jin-cai Wu; Yong-chun Liu
Journal:  J Fluoresc       Date:  2008-10-21       Impact factor: 2.217

5.  Influence of Amino Acid-Nucleobase Hybrid Ligand in Binding and Biological Activity of Co(II) and Zn(II) Complexes.

Authors:  V Violet Dhayabaran; T Daniel Prakash
Journal:  J Fluoresc       Date:  2016-07-15       Impact factor: 2.217

6.  Molecular aspects on the interaction of isatin-3-isonicotinylhydrazone to deoxyribonucleic acid: model for intercalative drug-DNA binding.

Authors:  Soheila Kashanian; Mohammad Mehdi Khodaei; Parvaneh Pakravan; Hadi Adibi
Journal:  Mol Biol Rep       Date:  2011-07-21       Impact factor: 2.742

7.  Two half-sandwiched ruthenium (II) compounds containing 5-fluorouracil derivatives: synthesis and study of DNA intercalation.

Authors:  Zhao-Jun Li; Yong Hou; Da-An Qin; Zhi-Min Jin; Mao-Lin Hu
Journal:  PLoS One       Date:  2015-03-19       Impact factor: 3.240

8.  Study on the Interaction between Isatin-β-Thiosemicarbazone and Calf Thymus DNA by Spectroscopic Techniques.

Authors:  Parvaneh Pakravan; Shahla Masoudian
Journal:  Iran J Pharm Res       Date:  2015       Impact factor: 1.696

9.  Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes.

Authors:  Palakuri Kavitha; K Laxma Reddy
Journal:  Bioinorg Chem Appl       Date:  2014-04-28       Impact factor: 7.778

  9 in total

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