Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786773
Title: Biosynthesis and metabolism of selected organofluorine compounds
Author: Rodil García, Andrea
ISNI:       0000 0004 7972 211X
Awarding Body: University of St Andrews
Current Institution: University of St Andrews
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
The St Andrews group has recently developed a range of novel fluorinated motifs, which include all-cis fluorocyclohexanes, difluoro oxy- and thio- ethers and α,β,β-trifluorocyclopropanes. Fluorinated motifs are often sought after in medicinal chemistry, and it became one of the aims of this thesis to explore these new motifs in order to assess their validity for drug discovery programmes. The metabolic stability of each motif was probed in incubations with Cunninghamella elegans. This fungus is well known for its ability to biotransform xenobiotics mimicking the mammalian P₄₅₀ profile, and thus, providing a useful model for metabolic vulnerability. This showed that the all-cis cyclohexyl derivatives were increasingly stable to the action of P₄₅₀'s with increasing fluorine substitution. The α,α-difluoro thioethers showed oxidation to sulfoxides and sulfones, and the difluorooxy analogue showed a rapid biodegradation into the corresponding acetate ester. The studied α,β,β-trifluorocyclopropanes proved challenging to isolate and identify, but it could be established that the fluorinated motif remained intact after the incubations. The enantioselectivity with which C. elegans transforms the products was explored by chiral HPLC, which allowed an estimation of the enantiomeric resolution of racemates, and also the enantioselectivity of sulfoxide formation. In both cases selectivities were relatively low. Additionally, the lipophilicity of the fluorinated motifs was calculated by reverse-phase HPLC. A general trend was that increasing fluorination led to increased polarity. A second aim was to explore the fluorometabolite biosynthesis in Streptomyces sp. MA37, isolated in Ghana (2014), which contains an active fluorinase. The metabolic pathway in Streptomyces sp. MA37 branches at 5-fluororibose phosphate (5-FDRP), allowing the formation of 5-fluoro-2,3,4-trihydroxypentanoic acid (5-FHPA) and other unknown metabolites. Each of the steps leading to 5-FHPA was studied, and the biotransformation was reconstituted in vitro. The production of fluorometabolites by Streptomyces sp. MA37 was investigated by carrying out cell-free and whole cell feeding experiments with [5',5'-²H₂]-5'-FDA. Incorporation into the fluorometabolites from [5',5'-²H₂]-5'-FDA was successful.
Supervisor: O'Hagan, David Sponsor: Seventh Framework Programme (European Commission) ; Marie Curie Initial Training Network FLUORINE21
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.786773  DOI: Not available
Keywords: Fluorine metabolism ; Fluorinase ; Cunninghamella elegans ; Streptomyces sp. MA37 ; QD412.F1R7 ; Organofluorine compounds--Synthesis ; Organofluorine compounds--Metabolism ; Biosynthesis ; Streptomyces
Share: