Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.794385
Title: Development of new synthetic inhibitors of Mycobacterium tuberculosis DprE2
Author: Chiodarelli, Giacomo
ISNI:       0000 0004 8499 5841
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2018
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Abstract:
DprE2 is an essential enzyme for Mycobacterium tuberculosis (M.tb); it is involved in the biosynthesis of decaprenyl monophosphoryl-D-arabinose, a central building block in the synthesis of key constituents of the mycobacterial cell wall. A hit-to-lead optimisation study of two DprE2 hits, discovered by GSK in a high-throughput, whole-cell phenotypic screen, is described. An indepth SAR study of these two hits highlighted the essentiality of the nitrofuran moiety in both structures for potency, and the need to retain the hydrazide moiety for DprE2 target engagement. These observations led us to propose that both hits function as prodrugs and are precursors of the bioactive metabolite(s). This hypothesis was confirmed in a recently developed DprE2 enzymatic assay, which revealed that both hits do not inhibit this enzyme. To probe this hypothesis further, the hits were shown to be substrates for a type I nitroreductase from E. coli. DprE 1 and Ddn are the only two enzymes that have been reported to bioactivate nitroaromatic drugs in M.tb; however, their involvement in the bioactivation of the DprE2 nitrofuran hits could be excluded. The selection of spontaneous resistant-mutants to the hits indicates the enzymes FGDl and FbiC are involved in mechanisms of resistance to the hits.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.794385  DOI: Not available
Keywords: QD Chemistry ; QH301 Biology
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