Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/301417
Title: Synthesis and In Vitro Evaluation of Heterocyclic Core Moieties as Anticancer Agents
Researcher: Verma, Meenakshi
Guide(s): Paul, Kamaldeep
Keywords: Anticancer
Naphthalimide
Pyridine
University: Thapar Institute of Engineering and Technology
Completed Date: 2015
Abstract: In present investigation, we have synthesized benzimidazole bearing naphthalimide analogues as well as N-allyl naphthalimides. These analogues were substituted with variety of primary and secondary amines. Keeping in mind, their DNA intercalating properties, UVVisible and fluorescence spectrophotometry and thermal denaturation experiments were performed with the most active compounds. Similarly, 2,3-disubstituted pyridine analogue appended 1,2,3-triazole motifs were synthesized. Characterization of these molecules was done with different spectroscopic techniques such as 1H NMR, 13C NMR and mass 126 spectroscopy. The synthesized molecules were evaluated in vitro over 60 human cancer cell lines. ct-DNA studies have been done for finding the probable interaction with DNA. Structure-activity relationship studies were used to identify the structural features of these novel compounds. In order to have an insight into the molecular interactions of these compounds, their docking were also planned to scrutinize the mode of interaction of compound with amino acids in the active site of the enzyme. newline
Pagination: 137p.
URI: http://hdl.handle.net/10603/301417
Appears in Departments:School of Chemistry and Biochemistry

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02_certificate.pdf3.71 MBAdobe PDFView/Open
03_candidates declaration.pdf3.71 MBAdobe PDFView/Open
04_acknowledgement.pdf3.71 MBAdobe PDFView/Open
05_table of contents.pdf3.72 MBAdobe PDFView/Open
06_introduction.pdf3.72 MBAdobe PDFView/Open
07_chapter 1.pdf3.72 MBAdobe PDFView/Open
08_chapter 2.pdf3.73 MBAdobe PDFView/Open
09_chapter 3.pdf3.73 MBAdobe PDFView/Open
10_chapter 4.pdf3.73 MBAdobe PDFView/Open
11_list of publications.pdf3.71 MBAdobe PDFView/Open
80_recommendation.pdf3.73 MBAdobe PDFView/Open
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