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dc.contributor.advisorSimanek, Eric E.
dc.contributor.authorLe, Tung
dc.date2016-12-18
dc.date.accessioned2016-12-19T22:09:19Z
dc.date.available2016-12-19T22:09:19Z
dc.date.issued2016
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/12257
dc.description.abstractBesides its commercial use as an anti-depressant, sertraline is also known to behave as an efflux pump inhibitor which impedes bacteria's ability to extrude antibiotic. This property explains why sertraline can potentiate clinically relevant antibiotics and make them effective against some resistant strains of bacteria. Exploiting this characteristic, a library of 2,4,6-trisubstituted-1,3,5-triazines were synthesized, using sertraline as one of the substituents while the other substituent groups were varied. The synthesized compounds were screened for antibacterial activities using Kirby-Bauer disk diffusion method. Of the seven new compounds prepared, three showed noteworthy activity against both Gram negative and Gram positive bateria, Staphylococcus aureus and Escherichia coli, respectively.
dc.titleSynthesis Of 2,4,6-Trisubstituted-1,3,5-Triazine Using Sertraline As One Of The Substituents
etd.degree.departmentChemistry
local.collegeCollege of Science and Engineering
local.collegeJohn V. Roach Honors College
local.departmentChemistry and Biochemistry
local.publicnoteFull text permanently unavailable by request of author. Contact author for access.


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