Synthesis, characterisation, molecular docking, biomolecular interaction and cytotoxicity studies of novel ruthenium(ii)–arene-2-heteroarylbenzoxazole complexes-Reference-Cited by-同舟云学术

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Synthesis, characterisation, molecular docking, biomolecular interaction and cytotoxicity studies of novel ruthenium(ii)–arene-2-heteroarylbenzoxazole complexes

Published:2019 Issue:8 Volume:43 Page:3291-3302
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

De Sourav¹²³^ORCID,Chaudhuri Shreya Ray¹²³,Panda Arpita¹²³,Jadhav Gajanan Rahosaheb¹²³,Kumar R. Selva¹²³^ORCID,Manohar Prasanth⁴⁵³,Ramesh N.⁴⁵³,Mondal Ashaparna¹²³,Moorthy Anbalagan⁴⁵³,Banerjee Subhasis⁶⁷³,Paira Priyankar¹²³^ORCID,Kumar S. K. Ashok¹²³^ORCID

Affiliation:

1. Department of Chemistry, School of Advance Sciences, Vellore Institute of Technology

2. Vellore-632014

3. India

4. Department of Biotechnology, School of Bioscience & Technology, Vellore Institute of Technology

5. Vellore 632014

6. Department of Pharmaceutical Chemistry, Gupta College of Technological Sciences

7. Asansol-713301

Abstract

Ru(ii)–arene-2-heteroarylbenzoxazole complexes were synthesized and implemented for their biological evaluation.

Funder

Department of Science and Technology, Ministry of Science and Technology

VIT University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ04999H

Reference84 articles.

1. Alteration of steric hindrance modulates glutathione resistance and cytotoxicity of three structurally related RuII-p-cymene complexes

2. DNA binding studies of 2-tert-butylhydroquinone (TBHQ) food additive

3. Biophysical analysis of natural, double-helical DNA modified by anticancer heterocyclic complexes of ruthenium(III) in cell-free media

4. The hydrolysis of the anti-cancer ruthenium complex NAMI-A affects its DNA binding and antimetastatic activity: an NMR evaluation

5. Redox behavior of tumor-inhibiting ruthenium(iii) complexes and effects of physiological reductants on their binding to GMP

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