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Synthesis of thioridazine-VLA-4 antagonist hybrids using N-propargyl northioridazine enantiomers

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Authors

Martyn, A. P.
Willis, Anthony
Kelso, Michael

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Taylor & Francis Group

Abstract

Herein, we report the synthesis of thioridazine-VLA-4 hybrid epimers. These hybrid molecules were obtained by means of a click reaction involving N-propargyl northioridazine enantiomers and an azide containing VLA-4 antagonist. A synthesis of northioridazine enantiomers from racemic thioridazine was developed and the absolute stereochemistry was confirmed by X-ray crystallography. Access to N-substituted thioridazine analogs may reveal that this phenothiazine core has therapeutic potential in other disease avenues.

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Synthetic Communications

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Restricted until

2099-12-31