Synthesis, characterization, antimicrobial, DNA-cleavage and antioxidant activities of 3-((5-chloro-2-phenyl-1 H -indol-3-ylimino)methyl)quinoline-2(1 H )-thione and its metal complexes

Vivekanand, B.; Raj, K. Mahendra; Mruthyunjayaswamy, B. H. M.

doi:10.1016/j.molstruc.2014.08.033

Cited by 43 publications

(18 citation statements)

References 43 publications

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“…Then the Schiff base complexes were synthesized using metal salts and the Schiff base. Antimicrobial and antioxidant studies, cyclic voltammetry of the complexes, and theoretical 1 H NMR and HOMO–LUMO energy calculations of the new bifunctional ligand were done …”

Section: Bioinorganic Chemistry: Synthesis Of Oxygen‐carrying Co Commentioning

confidence: 99%

Synthesis and antioxidant activities of Schiff bases and their complexes: a review

Zoubi

Al‐Hamdani

Kaseem

2016

Applied Organom Chemis

186

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Schiff bases, named after https://en.wikipedia.org/wiki/Hugo_Schiff, are aldehyde‐ or ketone‐like compounds in which the carbonyl group is replaced by imine or azomethine group. They are widely used for industrial purposes and also have a broad range of applications as antioxidants. An overview of antioxidant applications of Schiff bases and their complexes is discussed in this review. A brief history of the synthesis and reactivity of Schiff bases and their complexes is presented. Factors of antioxidants are illustrated and discussed. Copyright © 2016 John Wiley & Sons, Ltd.

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Section: Bioinorganic Chemistry: Synthesis Of Oxygen‐carrying Co Commentioning

confidence: 99%

Synthesis and antioxidant activities of Schiff bases and their complexes: a review

Zoubi

Al‐Hamdani

Kaseem

2016

Applied Organom Chemis

186

View full text Add to dashboard Cite

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“…Long-ago, contagious diseases caused by multidrug-resistant microorganisms have become a serious issue, representing a growing threat to human health and being a major problem in many countries worldwide. There has been a significant increase in clinical drug resistance over the past few decades, owing to exploitation of antimicrobial agents, thus many infectious disease can no longer be treated successfully with general anti-infective agents [ 17 ]. Modern therapies and management technique such as bone marrow or solid-organ transplants, and newer much aggressive chemotherapy have resulted in a rapidly inflating number of immune-suppressed patient.…”

Section: Biological Activities Of Thiazolidinediones Derivatives In Tmentioning

confidence: 99%

Biological potential of thiazolidinedione derivatives of synthetic origin

Sucheta

Tahlan

Verma

2017

Chemistry Central Journal

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Thiazolidinediones are sulfur containing pentacyclic compounds that are widely found throughout nature in various forms. Thiazolidinedione nucleus is present in numerous biological compounds, e.g., anti-malarial, antimicrobial, anti-mycobacterium, anticonvulsant, antiviral, anticancer, anti-inflammatory, antioxidant, anti-HIV (human immunodeficiency virus) and antitubercular agent. However, owing to the swift development of new molecules containing this nucleus, many research reports have been generated in a brief span of time. Therefore seems to be a requirement to collect recent information in order to understand the current status of the thiazolidinedione nucleus in medicinal chemistry research, focusing in particular on the numerous attempts to synthesize and investigate new structural prototypes with more effective antidiabetic, antimicrobial, antioxidant, anti-inflammatory, anticancer and antitubercular activity.

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“…However, when produced in excess, ROS can damage cell functionality as they can harm cellular lipids, proteins, and DNA [46]. Now days, interest is focused on the synthesis of new compounds with potential applications, such as cancer diagnosis and treatment of tumor [47].…”

Section: In Vitro Antioxidant Activity [C5h16n2](no3)2 (Mpn)mentioning

confidence: 99%

Synthesis, characterization, Hirshfeld surface analysis and antioxidant activity of a novel organic-inorganic hybrid material 1-methylpiperazine-1,4-diium bis(nitrate)

Gatfaoui

Mezni

Roisnel

et al. 2017

Journal of Molecular Structure

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A new organic-inorganic hybrid trioxonitrate was synthesized at room temperature.  The atomic arrangement shows three-dimensional network.  The crystal packing stabilized by a set of hydrogen bonds also analyzed by Hirshfeld surface.  This compound was investigated by IR spectroscopy.  Antioxidant study, in vitro, shows significant scavenging capacity of free radicals (DPPH• and ABTS•).

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Synthesis, characterization, antimicrobial, DNA-cleavage and antioxidant activities of 3-((5-chloro-2-phenyl-1 H -indol-3-ylimino)methyl)quinoline-2(1 H )-thione and its metal complexes

Cited by 43 publications

References 43 publications

Synthesis and antioxidant activities of Schiff bases and their complexes: a review

Synthesis and antioxidant activities of Schiff bases and their complexes: a review

Biological potential of thiazolidinedione derivatives of synthetic origin

Synthesis, characterization, Hirshfeld surface analysis and antioxidant activity of a novel organic-inorganic hybrid material 1-methylpiperazine-1,4-diium bis(nitrate)

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