Journal of Medicinal Chemistry · 2005 · 150 citations · 9 references
PharmacyBiochemistryMedicinal ChemistryBiochemical PharmacologyDrug DiscoverySynthetic Medicinal ChemistryChemoenzymatic SynthesisChiral SeparationProtein PhosphorylationBioactive Enantiomer IdentificationBiological CharacterizationEnantioselective SynthesisEnantioselectivityX-ray Diffraction AnalysisX-ray Diffraction Detection
In vivo phosphorylation of FTY720 (1) in rats and humans resulted exclusively in the biologically active (S)-configured enantiomer, which was proven by an ex vivo o-phthaldialdehyde derivatization protocol especially elaborated for phosphates of 1. Starting from the prochiral amino alcohol 1, racemic and enantiomerically pure phosphates of 1 were synthesized. Pure enantiomers were obtained after purification of a partially protected key intermediate on an enantioselective support. The absolute stereochemistry was determined by X-ray diffraction.
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