Publication | Open Access
Potent, Selective and Low-Calcemic Inhibitors of CYP24 Hydroxylase: 24-Sulfoximine Analogues of the Hormone 1α,25-Dihydroxyvitamin D<sub>3</sub>
105
Citations
11
References
2004
Year
PharmacotherapyChemical BiologyPharmaceutical ChemistryLow-calcemic InhibitorsDozen 24-Sulfoximine AnaloguesMolecular PharmacologyMedicinal ChemistryAnti-cancer AgentInhibitory ActivityBiochemistryMechanism Of ActionDrug DevelopmentPharmacologyPhenyl Sulfoximine 3A24-Sulfoximine AnaloguesCyp24 HydroxylaseCyp24 EnzymeNatural SciencesClinical PharmacologyMedicineDrug Discovery
A dozen 24-sulfoximine analogues of the hormone 1alpha,25-dihydroxyvitamin D(3) were prepared, differing not only at the stereogenic sulfoximine stereocenter but also at the A-ring. Although these sulfoximines were not active transcriptionally and were only very weakly antiproliferative, some of them are powerful hydroxylase enzyme inhibitors. Specifically, 24-(S)-NH phenyl sulfoximine 3a is an extremely potent CYP24 inhibitor (IC(50) = 7.4 nM) having low calcemic activity. In addition, this compound shows high selectivity toward the CYP24 enzyme in comparison to CYP27A1 (IC(50) > 1000 nM) and CYP27B (IC(50) = 554 nM).
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