Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/381746
Title: SYNTHESIS BIOACTIVITY OF 2HCHROMENE BASED FUNCTIONALIZED MOLECULES AND INCLUSION COMPLEX OF NITROCHROMENE WITH betaCD
Researcher: Mishra, N P
Guide(s): Mohapatra, Seetaram
Keywords: anti-inflammatories
Chemistry
Chemistry Applied
Heterocyclic molecules
pharmacological applications
Physical Sciences
University: Ravenshaw University
Completed Date: 2022
Abstract: Heterocyclic molecules implanted with nitrogen and oxygen atoms have been used in diverse biological and pharmacological applications [170]. Among different types of nitrogen and oxygen-containing heterocyclic compounds, five-membered heterocyclic compounds like azole, thiazole, oxadiazole, triazene, imidazole, purines, pyrazole etc. play a very important role in human life due to their medicinal action against several diseases [171-178]. Specifically, oxadiazole based compounds were found to exhibit anti-inflammatory, antimicrobial, antitubercular, antidepressant, antimalarial, anti-HIV, and anticancer properties [179-188]. Due to their biological activities, the synthesis of novel oxadiazole compounds is the current research area of interest to produce analgesics, antispasmodics and anti-inflammatories. Recently, our research group reported the microwave-assisted synthesis of chromene based 1,2,4-oxadiazole molecules having potent antibacterial activity [189]. Also, as reported earlier these oxadiazole nuclei contribute significant bioactivity due to their lipophilic nature and have the ability to bind with the target protein through hydrogen bonding [190]. Protein molecules play a crucial role in the effective action of several drugs in living beings [191]. The pharmacodynamics and pharmacokinetics of drugs generally depend on the binding of these molecules with albumin proteins [192-194]. Therefore, studying the binding mechanism responsible for the molecular interactions between drug molecules and albumin could help design new bioactive molecules. We selected bovine serum albumin (BSA) as a model protein for this study as it is largely present in the blood plasma and plays a vital role in the transportation of several endogenous and exogenous ligands (such as fatty acids, amino acids, steroids, and various drugs) [195]. Also, BSA is structurally similar (around 76%) to human serum albumin (HSA). It consists of 583 amino acid residues with a molecular weight of 66 kDa. BSA structure can be divided into three
Pagination: All Pages
URI: http://hdl.handle.net/10603/381746
Appears in Departments:Department of Chemistry

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06_list of graph and table.pdf.pdf7.43 MBAdobe PDFView/Open
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08_chapter 2.pdf.pdf3.77 MBAdobe PDFView/Open
09_chapter 3.pdf.pdf6.23 MBAdobe PDFView/Open
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80_recommendation.pdf350.7 kBAdobe PDFView/Open
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