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Nithya Balakrishnan

Researcher at National Institute of Technology, Tiruchirappalli

Publications -  10
Citations -  208

Nithya Balakrishnan is an academic researcher from National Institute of Technology, Tiruchirappalli. The author has contributed to research in topics: Chemistry & Ligand (biochemistry). The author has an hindex of 4, co-authored 6 publications receiving 66 citations.

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Synthesis and Anticancer Activity of [RuCl2(η6-arene)(aroylthiourea)] Complexes-High Activity against the Human Neuroblastoma (IMR-32) Cancer Cell Line.

TL;DR: The study concluded that the complexes promoted the oxidative stress-mediated apoptotic death of the cancer cells through the generation of intracellular ROS, depletion of MMP, and damage of the nuclear material.
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Impact of aliphatic acyl and aromatic thioamide substituents on the anticancer activity of Ru(II)-p-cymene complexes with acylthiourea ligands—in vitro and in vivo studies

TL;DR: In this paper, six different acylthiourea ligands (L1-L6) and their corresponding Ru(II)-p-cymene complexes (P1-P6) were designed to explore the structure-activity relationship of the complexes upon aliphatic chain and aromatic conjugation on the C- and N-terminals, respectively.
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Thiosemicarbazone(s)-anchored water soluble mono- and bimetallic Cu(II) complexes: enzyme-like activities, biomolecular interactions, anticancer property and real-time live cytotoxicity

TL;DR: The catecholase-mimicking activity of complexes 1-5 was examined spectrophotometrically, and the results revealed that all the complexes except 5 had the ability to oxidize 3, 5-di-tert-butylcatechol (3,5-DTBC) to 3,5 -di- tert- butylquinone (3-5-DTBQ) under aerobic conditions with moderate turnover numbers.
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Zinc(II) complexes of indole thiosemicarbazones: DNA/protein binding, molecular docking and in vitro cytotoxicity studies

TL;DR: Four Zn(II) complexes (1–4) featuring indole thiosemicarbazones were synthesized and well-characterized by elemental analyses and various spectroscopic techniques, which implied that the complexes bound to CT DNA via intercalation, and complex 4 showed a higher binding affinity than the other complexes.
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Tunable anticancer activity of furoylthiourea‐based Ru(II)‐arene complexes and their mechanism of action

TL;DR: In this paper, 14 RuII -arene (p-cymene/benzene) complexes (C1-C14) have been synthesized by varying the N-terminal substituent in the furoylthiourea ligand and satisfactorily characterized by using analytical and spectroscopic techniques.