Date of Award:
8-2019
Document Type:
Dissertation
Degree Name:
Doctor of Philosophy (PhD)
Department:
Chemistry and Biochemistry
Committee Chair(s)
Cheng-Wei Tom Chang
Committee
Cheng-Wei Tom Chang
Committee
Alvan C. Hengge
Committee
Lisa M. Berreau
Committee
Steve Scheiner
Committee
Jixun Zhan
Abstract
Adjacent cells communicate through gap junctions (GJs). These GJs are formed by head to head docking of two hemichannels (HCs) from two adjacent cells. HCs are connexin hexamer proteins. Connexin mutation is the most frequent cause of childhood hearing loss. This hearing impairment affects 2 in every 2000 children. Inhibition of the HCs might be the key factor to treat such disorders. A library of amphiphilic kanamycins was synthesized to be tested as HC inhibitors. These compounds showed excellent inhibition activity in comparison with the parent compound (kanamycin A) with less toxicity.
A library of monosaccharide esters with varying carbon chain lengths (acetyl (C2) to hexadecyl (C16)) were synthesized, characterized, and tested for bioactivity. Carbohydrate esters showed low toxicity while remaining active against bacteria and fungi. The compound 6-O-tetradecanoyl-D-mannopyranose (MAN014), a mannose ester with a fourteen-carbon chain, showed the greatest antibacterial and antifungal properties. A mode of action study was tested against Staphylococcus aureus (bacteria) and Fusarium graminearum (fungus) and found the compound perturbed the cell membrum.
Checksum
4dd843f46bdac5e9c0ff6e17dbfa6219
Recommended Citation
Alfindee, Madher N., "Synthesis and Biological Studies of Amphiphilic Compounds Derived from Saccharides and Aminoglycosides" (2019). All Graduate Theses and Dissertations, Spring 1920 to Summer 2023. 7568.
https://digitalcommons.usu.edu/etd/7568
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