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1.
J Labelled Comp Radiopharm ; 59(4): 175-86, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26991121

ABSTRACT

The 24th annual symposium of the International Isotope Society's United Kingdom Group took place at the Møller Centre, Churchill College, Cambridge, UK on Friday 6th November 2015. The meeting was attended by 77 delegates from academia and industry, the life sciences, chemical, radiochemical and scientific instrument suppliers. Delegates were welcomed by Dr Ken Lawrie (GlaxoSmithKline, UK, chair of the IIS UK group). The subsequent scientific programme consisted of oral presentations, short 'flash' presentations in association with particular posters and poster presentations. The scientific areas covered included isotopic synthesis, regulatory issues, applications of labelled compounds in imaging, isotopic separation and novel chemistry with potential implications for isotopic synthesis. Both short-lived and long-lived isotopes were represented, as were stable isotopes. The symposium was divided into a morning session chaired by Dr Rebekka Hueting (University of Oxford, UK) and afternoon sessions chaired by Dr Sofia Pascu (University of Bath, UK) and by Dr Alan Dowling (Syngenta, UK). The UK meeting concluded with remarks from Dr Ken Lawrie (GlaxoSmithKline, UK).

2.
Bioorg Med Chem ; 20(18): 5658-67, 2012 Sep 15.
Article in English | MEDLINE | ID: mdl-22890009

ABSTRACT

The syntheses of stable isotope labelled internal standards of important CYP-isoform selective probes, like testosterone 1, diclofenac 3, midazolam 5, and dextromethorphan 7, as well as their corresponding hydroxylated metabolites 6ß-hydroxytestosterone 2, 4'-hydroxydiclofenac 4, 1'-hydroxymidazolam 6 and dextrorphan 8 are reported. Microwave-enhanced H/D-exchange reactions applying either acid, base, or homogeneous and heterogeneous transition metal catalysis, or combinations thereof proved to be highly efficient for direct deuterium labelling of the above mentioned probes. Compared to conventional stepwise synthetic approaches, the combination of H/D exchange and biotransformation provides the potential for considerable time- and cost savings, in particular for the synthesis of the stable isotope labelled internal standards of 4'-hydroxydiclofenac 4 and 1'-hydroxymidazolam 6.


Subject(s)
Diclofenac/analogs & derivatives , Isotope Labeling/methods , Midazolam/analogs & derivatives , Pharmaceutical Preparations/chemistry , Cytochrome P-450 Enzyme System/metabolism , Deuterium Exchange Measurement , Diclofenac/chemical synthesis , Diclofenac/chemistry , Diclofenac/metabolism , Microwaves , Midazolam/chemical synthesis , Midazolam/chemistry , Midazolam/metabolism , Molecular Structure , Pharmaceutical Preparations/metabolism , Reference Standards
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