Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3965
Title: Anticancer effects of novel tetrahydro-dimethyl-xanthene-diones
Authors: Alagumuthu, Manikandan
Keywords: 3,4,6,7 tetrahydro 3,3 dimethyl 9 phenyl 2h xanthene 1,8(5h,9h) dione;doxorubicin;phosphatidylinositol 3 kinase;tetrahydro dimethyl xanthene dione;unclassified drug;xanthene derivative;antineoplastic agent;xanthene derivative;antineoplastic activity;antioxidant activity;Article;BT-474 cell line;cell viability assay;colorimetry;computer model;controlled study;cytotoxicity;drug absorption;drug distribution;drug efficacy;drug excretion;drug metabolism;drug toxicity;enzyme activity;enzyme inhibition assay;enzyme linked immunosorbent assay;human;human cell;hydrogen peroxide scavenging assay;in vitro study;K-562 cell line;MCF-7 cell line;molecular docking;molecular interaction;MTT assay;oxidative stress;pharmacokinetic parameters;cell proliferation;cell survival;chemical structure;chemistry;dose response;drug effect;drug screening;structure activity relation;tumor cell line;Antineoplastic Agents;Cell Line, Tumor;Cell Proliferation;Cell Survival;Dose-Response Relationship, Drug;Drug Screening Assays, Antitumor;Humans;K562 Cells;Molecular Docking Simulation;Molecular Structure;Structure-Activity Relationship;Xanthenes
Issue Date: 2020
Publisher: Bentham Science Publishers
Citation: Manikandan, A., Sivakumar, A., Nigam, P. S., & Napoleon, A. A. (2020). Anticancer effects of novel tetrahydro-dimethyl-xanthene-diones. Anti-Cancer Agents in Medicinal Chemistry, 20(7), 909-916. doi:10.2174/1871520620666200318094138
Abstract: Background: The derivatives of xanthene are known to have promising anticancer properties, in comparison to xanthene itself. Objective: The object of our study was to develop few xanthene derivatives (a family of fifteen novel 3,4,6,7-tetrahydro-3,3-dimethyl-9-phenyl-2H-xanthene-1,8(5H, 9H)-diones encoded as 4a-4m), which were effectively prepared through regioselective synthesis approach, and to test their anticancer effects. Methods: A series of cell lines were used in this study, first to assess the cytotoxicity and then the drug efficacy of target compounds, consecutively. Prior to MTT assay, the compounds were analysed for their antioxidant properties, since oxidative stress is an important factor in the development of many cancer types. The anticancer properties of 4a-m have been assessed over in silico (molecular docking and ADMET assessments) and in vitro (MTT assay) methods. Results: Compounds 4h and 4i showed a relative percentage anticancer activity of 86.25±1.25 & 89.74±1.64 against BT474 (ER+HER2+), and 90.56±1.18 & 93.24±1.80 against MCF-7 (ER-HER2), respectively. Conclusion: The animal model and pre-clinical studies for 4h and 4i should be performed in order to develop them as future anticancer agents. © 2020 Bentham Science Publishers.
URI: https://doi.org/10.2174/1871520620666200318094138
https://dspace.iiti.ac.in/handle/123456789/3965
ISSN: 1871-5206
Type of Material: Journal Article
Appears in Collections:Department of Biosciences and Biomedical Engineering

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: