Literature DB >> 24904962

New mixed ligand zinc(II) complexes based on the antiepileptic drug sodium valproate and bioactive nitrogen-donor ligands. Synthesis, structure and biological properties.

Mohanad Darawsheh1, Hijazi Abu Ali2, A Latif Abuhijleh1, Emilia Rappocciolo3, Mutaz Akkawi4, Suhair Jaber4, Salam Maloul1, Yasmeen Hussein3.   

Abstract

Starting from the precursor [Zinc Valproate complex] (1), new mixed ligand zinc(II) complexes of valproic acid and nitrogen-based ligands, formulating as, [Zn(valp)22,9-dmphen] (2), [Zn2(valp)4(quin)2] (3), [Zn(valp)2(2-ampy)2] (4), and [Zn(valp)2(2-ampic)2] (5) (valp = valproate, 2,9-dmphen = 2,9-dimethyl-1,10-phenanthroline, quin = quinoline, 2-ampy = 2-aminopyridine, 2-ampic = 2-amino-6-picoline) were synthesized and characterized using IR, (1)H NMR, (13)C{(1)H} NMR and UV-Vis spectrometry. The crystal structures of complexes 2, 3 and 4 were determined using single-crystal X-ray diffraction. The complexes were also evaluated for their anti-bacterial activity using in-vitro agar diffusion method against three Gram-positive (Micrococcus luteus, Staphylococcus aureus, and Bacillus subtilis) and three Gram-negative (Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis) species. Complex 2 showed considerable activity against all tested microorganisms and the effect of complexation on the anti-bacterial activity of the parent ligand of 2 was also investigated. The anti-bacterial activity of 2,9-dmphen against Gram-negative bacteria was enhanced upon complexation with zinc valproate. On the other hand, complexes 1 and 3 showed weak inhibition activity against the tested species and complexes 4 and 5 didn't show any activity at all. Two methods were used for testing the inhibition of ferriprotoporphyrinIX bio-mineralization: a semi-quantitative micro-assay and a previously self-developed quantitative in-vitro method. Both were used to study the efficiency of these complexes in inhibiting the formation of the Malaria pigment which considered being the target of many known anti-malarial drugs such as Chloroquine and Amodiaquine. Results showed that the efficiency of complex 2 in preventing the formation of β-Hematin was 80%. The efficiency of Amodiaquine as a standard drug was reported to give 91%.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

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Keywords:  Anti-bacterial activity; Anti-malarial activity; Hemozoin; Nitrogen-based ligands; Valproic acid; Zinc(II) complexes; β-Hematin

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Year:  2014        PMID: 24904962     DOI: 10.1016/j.ejmech.2014.01.067

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  2 in total

1.  Nitrogen donor ligand for capping ZnS quantum dots: a quantum chemical and toxicological insight.

Authors:  Vivek Pandey; Vinay Kumar Tripathi; Keshav Kumar Singh; Tejasvi Bhatia; Nitesh Kumar Upadhyay; Bela Goyal; Gajanan Pandey; Inho Hwang; Poonam Tandon
Journal:  RSC Adv       Date:  2019-09-11       Impact factor: 4.036

2.  Synthesis, crystallographic, spectroscopic studies and biological activity of new cobalt(II) complexes with bioactive mixed sulindac and nitrogen-donor ligands.

Authors:  Asia M Shalash; Hijazi I Abu Ali
Journal:  Chem Cent J       Date:  2017-05-10       Impact factor: 4.215

  2 in total

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