Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3965
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dc.contributor.authorAlagumuthu, Manikandanen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-17T15:31:10Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-17T15:31:10Z-
dc.date.issued2020-
dc.identifier.citationManikandan, 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:10.2174/1871520620666200318094138en_US
dc.identifier.issn1871-5206-
dc.identifier.otherEID(2-s2.0-85086148378)-
dc.identifier.urihttps://doi.org/10.2174/1871520620666200318094138-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/3965-
dc.description.abstractBackground: 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.en_US
dc.language.isoenen_US
dc.publisherBentham Science Publishersen_US
dc.sourceAnti-Cancer Agents in Medicinal Chemistryen_US
dc.subject3,4,6,7 tetrahydro 3,3 dimethyl 9 phenyl 2h xanthene 1,8(5h,9h) dioneen_US
dc.subjectdoxorubicinen_US
dc.subjectphosphatidylinositol 3 kinaseen_US
dc.subjecttetrahydro dimethyl xanthene dioneen_US
dc.subjectunclassified drugen_US
dc.subjectxanthene derivativeen_US
dc.subjectantineoplastic agenten_US
dc.subjectxanthene derivativeen_US
dc.subjectantineoplastic activityen_US
dc.subjectantioxidant activityen_US
dc.subjectArticleen_US
dc.subjectBT-474 cell lineen_US
dc.subjectcell viability assayen_US
dc.subjectcolorimetryen_US
dc.subjectcomputer modelen_US
dc.subjectcontrolled studyen_US
dc.subjectcytotoxicityen_US
dc.subjectdrug absorptionen_US
dc.subjectdrug distributionen_US
dc.subjectdrug efficacyen_US
dc.subjectdrug excretionen_US
dc.subjectdrug metabolismen_US
dc.subjectdrug toxicityen_US
dc.subjectenzyme activityen_US
dc.subjectenzyme inhibition assayen_US
dc.subjectenzyme linked immunosorbent assayen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjecthydrogen peroxide scavenging assayen_US
dc.subjectin vitro studyen_US
dc.subjectK-562 cell lineen_US
dc.subjectMCF-7 cell lineen_US
dc.subjectmolecular dockingen_US
dc.subjectmolecular interactionen_US
dc.subjectMTT assayen_US
dc.subjectoxidative stressen_US
dc.subjectpharmacokinetic parametersen_US
dc.subjectcell proliferationen_US
dc.subjectcell survivalen_US
dc.subjectchemical structureen_US
dc.subjectchemistryen_US
dc.subjectdose responseen_US
dc.subjectdrug effecten_US
dc.subjectdrug screeningen_US
dc.subjectstructure activity relationen_US
dc.subjecttumor cell lineen_US
dc.subjectAntineoplastic Agentsen_US
dc.subjectCell Line, Tumoren_US
dc.subjectCell Proliferationen_US
dc.subjectCell Survivalen_US
dc.subjectDose-Response Relationship, Drugen_US
dc.subjectDrug Screening Assays, Antitumoren_US
dc.subjectHumansen_US
dc.subjectK562 Cellsen_US
dc.subjectMolecular Docking Simulationen_US
dc.subjectMolecular Structureen_US
dc.subjectStructure-Activity Relationshipen_US
dc.subjectXanthenesen_US
dc.titleAnticancer effects of novel tetrahydro-dimethyl-xanthene-dionesen_US
dc.typeJournal Articleen_US
dc.rights.licenseAll Open Access, Green-
Appears in Collections:Department of Biosciences and Biomedical Engineering

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