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The University of Arizona.

The Discovery and Synthesis of Novel DYRK1A Inhibitors for Various Oncologic Targets

Abstract

dc:description.abstract

This dissertation describes the research of small molecule kinase inhibitors focused on in silico design, targeted synthesis, and their biological evaluation for the interest in translational medicinal chemistry projects with an emphasis in oncology. The first project (Chapter 1) is the identification and synthesis of novel “6,5” heterocycle based dual specificity tyrosine phosphorylation regulated kinase-1A (DYRK1A) as a potential treatment approach for certain DYRK associated pathologies. A series of Groebke–Blackburn–Bienaymé (GBB) based analogs were synthesized and assessed, showing somewhat promising activity. Further profiling of this series has led to a potential in vivo candidate DYR794 (49) and has revealed a new series of urea-based linkers which provide an opportunity for further exploration of other kinases and Poly-pharmacology approaches. The second project (Chapter 2) is focused on the development of Glial Blastoma Multiforme (GBM) based “6,6 Aryl-Pip” quinazoline based analogs. These compounds serendipitously inhibit key GBM relevant kinases as a novel approach to treat this specific cancer. A series of molecules were made and analyzed in revealing potential IND candidates and in vivo candidates that are orally bioavailable. The intent of the third project (Chapter 3) is the synthesis of low nanomolar WNT-pathway inhibitors for the treatment of Colorectal Cancer (CRC). These “6,6 Pip-Aryl” quinazoline based inhibitors showcased promising activity in both CRC and GBM cell lines with a clear direction for in vivo candidacy. This series binds to higher order cyclin dependent kinases (CDKs) which help regulate DNA transcription.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
doctoral
Discipline thesis:degree_discipline
Graduate College
Grantor dc:publisher
The University of Arizona.
Year dc:date.issued
2025

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Chavez, Timothy
Advisors dc:contributor.advisor
  • CARTMELL, CHRISTOPHER
  • Lee, Nam Yong
Committee members dc:contributor.committeemember
  • McGrath, Dominic V.
  • Tomasiak, Thomas M.

Rights

dc:rights
Statement dc:rights
  • Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction, presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10150/677518
OAI identifier oai:identifier
oai:repository.arizona.edu:10150/677518

Chain of custody

source
Harvested from
University of Arizona
Base URL
repository.arizona.edu/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Chavez, Timothy. The Discovery and Synthesis of Novel DYRK1A Inhibitors for Various Oncologic Targets. doctoral thesis, The University of Arizona., 2025. http://hdl.handle.net/10150/677518