Thesis

Novel approaches targeting phosphoinositide 3-kinase delta

Creator
Rights statement
Awarding institution
  • University of Strathclyde
Date of award
  • 2018
Thesis identifier
  • T16141
Person Identifier (Local)
  • 201484454
Qualification Level
Qualification Name
Department, School or Faculty
Abstract
  • This thesis explores the development of inhibitors for phosphoinositide 3-kinase δ(PI3Kδ), a lipid kinase implicated in COPD related inflammation. Firstly, a macrocyclisation approach was explored (Figure 1), this involved design,synthesis and profiling of macrocyclic analogues of the ‘benzoxazine’ series of PI3Kδinhibitors. This approach showed macrocycles could provide lead-like compounds,with a number of macrocycles exhibiting potency gains, up to 200-fold, over acyclic progenitor compounds. Next, the effect of macrocyclisation on other relevant properties for drug discovery was examined. It was established that a number of these macrocycles are water soluble, permeable, low clearance compounds. Differences with acyclic compounds were observed in subsets of compounds, however broad conclusions about the effect of macrocyclisation could not be drawn.In the second part of this study, synthetic methodology was developed for the synthesis of cyclopropyl boronic esters (Figure 2). Synthesis of compounds containing this functionality allows facile incorporation of three-dimensional character into drug-like scaffolds. A reaction manifold was developed utilising Schwartz’s Reagent for the conversion of synthetically tractable propargylic silyl ethers into complex products ina one-pot procedure, exemplified by the synthesis of aryl-, aliphatic-, quaternary- and spiro- substituted cyclopropyl boronic esters. The methodology was applied to enable a new synthesis of biologically active Sedaxane, via a bis-cyclopropyl boronic ester motif and to explore a growth vector from a cyclopropyl ring in an emerging series of PI3Kδ inhibitors.
Advisor / supervisor
  • Jamieson, Craig
  • Talbot, Eric
  • Hardy, Charlotte
Resource Type
Note
  • Previously held under moratorium in Chemistry Department (GSK) from 16 May 2018 until 18 June 2021.
  • Please note the confidentiality statement on each page of this thesis DOES NOT apply.
DOI
Alternative Title
  • Novel approaches targeting phosphoinositide 3-kinase δ
  • Novel approaches targeting PI3Kδ
Funder
Embargo Note
  • This thesis is restricted to Strathclyde users only until 16 May 2023.

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