In this thesis Colm Duffy reviews the chemistry and biology of
stable lipoxin analogues. Colm has prepared for the first time ever
a pyridine-containing LXA4 analogue in enantiomerically pure form.
Biological evaluation determined that both epimers at the benzylic
position suppress key cytokines known to be involved in
inflammatory disease, with the (R)-epimer proving most efficacious.
Moreover the author developed an excellent route to a related
thiophene-containing analogue that also showed interesting
biological activity. Both routes have inspired further work in the
synthesis of further heteroaromatic analogues for biological
evaluation. "
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