Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703512
Title: The untargeted kinome : building chemical capacities and bridges in cancer research
Author: Beltrán Molina, Maria Dolores
ISNI:       0000 0004 6062 0332
Awarding Body: University of Strathclyde
Current Institution: University of Strathclyde
Date of Award: 2016
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Abstract:
This thesis describes our efforts to design and synthesize selective probes for the PIM kinases (PIM-1, PIM-2, and PIM-3), because of their important role in cancer. During the course of the investigation we also examined the splicing kinases CLK1, CLK3, CLK4, DYRK1, DYRK2, SRPK1, and SRPK2. In Chapter 2, SAR and molecular modelling studies were carried out using a known benzothienopyrimidinone PIM inhibitor1 (J. Med. Chem., 2009, 52, 6621-6636). A series of analogues were synthesized providing low nanomolar activities towards the PIM kinases but showing little selectivity between the isoforms. Within these studies on PIM selectivity, the discovery of potential CLK4 chemical probes was made, which led to the first CLK4 X-ray crystal structure with a compound bound within the ATP binding site. Chapter 3 describes the discovery of a new series of compounds containing a phenyl pyrimidinone core which showed excellent activity against the PIM kinases. The scaffold offered potential for multiple points of diversity and applications in future programmes. A one-pot strategy for the synthesis of the phenyl pyrimidinone core is also described. Chapter 4 presents the discovery of a benzothienodiazepine scaffold. Through SAR studies, molecular modeling, and biological evaluation, potential PIM-1 and PIM-3 selective probes with good selectivity as well as low nanomolar activities are discussed. An X-ray crystal structure of PIM-1 with one of our analogues is also described, confirming that the compound is bound in the PIM-1 ATP binding pocket. Chapter 5 describes the biological evaluation carried out with the potential PIM-1 and PIM-3 selective probes. Solubility, permeability, in vitro and in vivo assays are detailed, providing low nanomolar activities as well as excellent selectivity towards a wide panel of kinases. Selected probes are further being characterized. On validation, our aim is to make these probes available to the biological community in order to dissect the fundamental biology of these important receptors.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.703512  DOI: Not available
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