Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/572329
Title: Possible anticancer activity of a synthetic nitro flavone derivative 2 4 nitrophenyl 4h chromen 4 one
Researcher: Mitra, Anindita
Guide(s): Ghosh, Rita
Keywords: Biochemistry and Molecular Biology
Biology and Biochemistry
Cancer
Flavonoids
Life Sciences
University: University of Kalyani
Completed Date: 2021
Abstract: Flavonoids are a group of low molecular weight polyphenolic compounds synthesized in plants as secondary metabolites for their protection against UV radiation, attacks from fungi and insects. They exhibit several biochemical and pharmacological effects; hence these classes of molecules have attracted interest of researchers for the study of their biological activities. Flavonoids are classified mainly depending on the level of oxidation and pattern of substitution in the C ring, while individual compounds within a class differ in the pattern of substitution of the A and B rings. Among them, the flavone moiety forms an important backbone. These low molecular weight compounds have several health promoting effects and possess significant biological effects that include antioxidant, anti-inflammatory, antibacterial and antifungal properties. Importantly, some flavones are also known to be effective in therapy of different cancers. Besides the natural derivatives of flavones, significant modifications of the flavone ring have yielded several synthetic flavone derivatives that have shown improved anticancer properties than their natural counterparts. newline
Pagination: 371p.
URI: http://hdl.handle.net/10603/572329
Appears in Departments:Biochemistry and Biophysics

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04_abstract.pdf385.8 kBAdobe PDFView/Open
05_chapter-1.pdf1.45 MBAdobe PDFView/Open
06_chapter-2.pdf2.87 MBAdobe PDFView/Open
07_chapter-3.pdf2.12 MBAdobe PDFView/Open
08_chapter-4.pdf3.46 MBAdobe PDFView/Open
09_chapter-5.pdf2.91 MBAdobe PDFView/Open
10_chapter-6.pdf2.27 MBAdobe PDFView/Open
11_annexures.pdf18.18 MBAdobe PDFView/Open
80_recommendation.pdf2.64 MBAdobe PDFView/Open
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