<p><span style="font-size: small;">Spectro-analytical and In Vitro Biological Studies of Novel Nalidixic acid Hydrazone and Its Transition Metal Complexes</span></p>
Online Publishing @ NISCAIR
View Archive InfoField | Value | |
Authentication Code |
dc |
|
Title Statement |
<p><span style="font-size: small;">Spectro-analytical and In Vitro Biological Studies of Novel Nalidixic acid Hydrazone and Its Transition Metal Complexes</span></p> |
|
Added Entry - Uncontrolled Name |
Narsimha, Nagula ; Osmania University Jaheer, Mohmed ; Osmania University Ranjith Reddy, Palreddy ; Osmnaia University Sudeepa, Kunche ; Osmania University Sarala Devi, CH ; Department of Chemistry Osmania University University Grant Commission, New Delhi, India |
|
Uncontrolled Index Term |
Nalidixic acid; Antimicrobial activity; DNA interactions; MTT assay; Molecular docking. |
|
Summary, etc. |
<p>The novel and potential chelating agent derived from Nalidixic acid and its binary Cu(II), Ni(II) and Co(II) metal complexes have been synthesized and characterized by elemental analyses, <sup>1</sup>H-NMR, Mass, UV-Vis, FT-IR, TGA, SEM-EDX, ESR and magnetic susceptibility measurements. All the systems of present study screened for antimicrobial activity against bacterial species <em>Bacillus</em> <em>(Gram +) </em>and <em>Escherichia coli</em> <em>(Gram -)</em> and fungal species <em>Sclerotium rolfsii</em> and <em>Macrophomina phaseolina</em> inferred enhanced activity in metal complexes over unbound free chelating agent. The interaction studies of metal complexes with Calf-thymus DNA (CT-DNA) investigated by UV-Visible and fluorescence titrations revealed the intercalation mode of binding. The interaction of compounds with CT-DNA evaluated for nucleage activity by agarose gel electrophoresis assay indicated their potential cleavage property. Further MTT assay performed on HeLa (human cervical cancer) and A549 (human lung tumor) cell lines revealed the IC<sub>50 </sub>values for title compounds studied. In addition computer-aided molecular docking technique carried out with all title compounds employing molecular target DNA (PDB ID: 1N37) furnished docking scores and mode of binding for geometry optimized molecular structures of title compounds.</p> |
|
Publication, Distribution, Etc. |
Indian Journal of Chemistry -Section A (IJCA) 2020-10-12 16:05:32 |
|
Electronic Location and Access |
application/pdf http://op.niscair.res.in/index.php/IJCA/article/view/21794 |
|
Data Source Entry |
Indian Journal of Chemistry -Section A (IJCA); ##issue.vol## 58, ##issue.no## 4 (2019): INDIAN JOURNAL OF CHEMISTRY- SECTION A |
|
Language Note |
en |
|
Nonspecific Relationship Entry |
http://op.niscair.res.in/index.php/IJCA/article/download/21794/465468195 http://op.niscair.res.in/index.php/IJCA/article/download/21794/465468197 http://op.niscair.res.in/index.php/IJCA/article/download/21794/465468199 |
|
Terms Governing Use and Reproduction Note |
Except where otherwise noted, the Articles on this site are licensed under Creative Commons License: CC Attribution-Noncommercial-No Derivative Works 2.5 India© 2015. The Council of Scientific & Industrial Research, New Delhi. |
|