Date of Award

Spring 6-12-2026

Document Type

Masters Thesis

Degree Name

M.S. in Chemistry and Biochemistry

Organizational Unit

College of Natural Science and Mathematics, Chemistry and Biochemistry

First Advisor

Sunil Kumar

Second Advisor

Brian Michel

Third Advisor

Scott Horowitz

Fourth Advisor

Daniel Linseman

Copyright Statement / License for Reuse

All Rights Reserved
All Rights Reserved.

Keywords

Interactions, Neurodegenerative, Oligopyridyl, Protein, Synthesis

Abstract

Protein-Protein Interactions are the foundation of many regulatory processes in physiological systems. Perturbations in these processes such as mutations or conditional cellular stress can cause the mutation or misfolding of essential proteins, leading to aberrant Protein-Protein Interactions (aPPIs) that have cascading negative effects on essential biochemical processes. aPPIs are implicated as the leading cause and progressor of neurodegenerative diseases, particularly Parkinson’s, Alzheimer’s, ALS, and Huntington’s Disease. While many attempts at therapeutic treatments for neurodegenerative diseases have emerged in the last 30 years, the modulation of disease related aPPIs has proven to be a demanding and complex task as the interactions between relevant proteins occur between a large variety of chemical moieties and protein surface areas.

Chemically diverse synthetic libraries of organic compounds have recently been employed to nullify aPPIs in vitro and in vivo. Previous libraries of compounds have proven both synthetically difficult and relatively non-scalable. In this work, we present a family of Oligopyridyl (OP) compounds that are synthetically trivial, scalable, and potent antagonists of relevant aPPIs in the human brain.

Copyright Date

6-2026

Publication Statement

Copyright is held by the author. User is responsible for all copyright compliance.

Rights Holder

George Cole Jernigan

Provenance

Received from ProQuest

File Format

application/pdf

Language

English (eng)

Extent

160 pgs

File Size

5.2 MB

Available for download on Friday, August 11, 2028



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