Files in this item

FilesDescriptionFormat

application/pdf

application/pdfSAWYER-THESIS-2021.pdf (2MB)Restricted Access
(no description provided)PDF

Description

Title:Discovery of covalent modifiers via the complexity to diversity strategy
Author(s):Sawyer, Adam Michael
Advisor(s):Hergenrother, Paul J
Department / Program:Chemistry
Discipline:Chemistry
Degree Granting Institution:University of Illinois at Urbana-Champaign
Degree:M.S.
Genre:Thesis
Subject(s):Covalent modifiers
targeted covalent inhibitors
complexity to diversity
complex molecule synthesis
Abstract:Targeted covalent drugs have recently become integral parts of drug discovery. Given the advantages of high-throughput screening in drug discovery, many electrophilic fragment collections have been developed as a promising alternative to discover and validate novel targets. However, most covalent screening libraries consist of flat, low molecular weight compounds that are lacking in complexity and are incapable of addressing more complex targets, such as protein-protein interactions. To fill this gap, a library of 19 complex and diverse compounds containing electrophilic moieties has been synthesized and screened for anticancer activity in cell culture. The results from these studies suggest the potential for electrophilic natural product-like compounds to be used in the investigation of biological targets implicated in cancer.
Issue Date:2021-04-29
Type:Thesis
URI:http://hdl.handle.net/2142/110875
Rights Information:Copyright 2021 Adam Sawyer
Date Available in IDEALS:2021-09-17
Date Deposited:2021-05


This item appears in the following Collection(s)

Item Statistics