Synthesis and Biological Activities of Aspirin-Azo Derivatives

Ho, Boon Kui (2017) Synthesis and Biological Activities of Aspirin-Azo Derivatives. Masters thesis, Universiti Malaysia Sarawak.

[img] PDF (Please get the password from TECHNICAL & DIGITIZATION MANAGEMENT UNIT, ext: 082-583913/ 082-583914)
Ho Boon Kui.pdf
Restricted to Registered users only

Download (6MB)

Abstract

The chemistry of aspirin and azo derivatives has been widely studied for pharmaceutical purposes. In this study, a series of halogenated azo derivatives 47-49(a-d) and aspirinhalogenated azo derivatives 50-52(a-d) were successfully synthesised. Halogenated azo derivatives 47-49(a-d) were synthesized via coupling reaction while aspirin-halogenated azo derivatives 50-52(a-d) were synthesised via esterification reaction of aspirin with 47- 49(a-d). The structures of all the synthesized compounds were characterized by using elemental analysis (CHNS), nuclear magnetic resonance (1H NMR and 13C NMR) and Fourier Transform infrared (FTIR) spectroscopies. All compounds were evaluated for antibacterial activities against Escherichia coli ATCC 25922 and Staphylococcus aureus S48/81 via turbidimetric kinetic method. Compounds 47-49(a-d) showed good antibacterial activity against E. coli and S. aureus due to the presence of halogen substituents and -N=N- groups, which played significant role in antibacterial activities. The synthesised aspirin–halogenated azo derivatives 50-52(a-d) showed weak antibacterial activity against tested bacteria due to bulky molecular structure thus hindered the penetration into bacterial cell wall. All compounds were also further screened for their anticancer activities against nasopharyngeal cancer cell lines HK-1 using MTS [3-(4,5- dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide]-based colorimetric assay. Among 47-49(a-d), compound 47a and 49a showed good cell inhibition against HK-1. Aspirin–halogenated azo derivatives 50-52(a-d), on the other hand, exhibited weak cancer cells inhibition due to possible weak binding into EGFR tyrosine kinase.

Item Type: Thesis (Masters)
Additional Information: Thesis (M.Sc.) -- Universiti Malaysia Sarawak, 2017.
Uncontrolled Keywords: aspirin, azo derivatives, antibacterial activity, E.coli, S.aureus, anticancer activity, HK-1 nasopharyngeal cancer cell lines, unimas, university, universiti, Borneo, Malaysia, Sarawak, Kuching, tourist management, Samarahan, ipta, education, Postgraduate, research, Universiti Malaysia Sarawak.
Subjects: Q Science > QD Chemistry
Divisions: Academic Faculties, Institutes and Centres > Faculty of Resource Science and Technology
Depositing User: Karen Kornalius
Date Deposited: 08 Mar 2019 02:42
Last Modified: 10 Nov 2021 07:40
URI: http://ir.unimas.my/id/eprint/23865

Actions (For repository members only: login required)

View Item View Item