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1<i>α</i>,24(<i>S</i>)-dihydroxyvitamin D2: a biologically active product of 1<i>α</i>-hydroxyvitamin D2 made in the human hepatoma, Hep3B
61
Citations
18
References
1995
Year
Medicinal ChemistryHuman HepatomaHepatologyBiochemistryAlpha-hydroxyvitamin D2Liver PhysiologyMedicineActive ProductNatural SciencesHepatotoxicityVitamin B ComplexVitamin D ReceptorMetabolomicsMetabolismPharmacologyVitamin DOxidative Stress
A major metabolite of the vitamin D analogue 1 alpha-hydroxyvitamin D2 in human liver cells in culture has been identified as 1 alpha,24(S)-dihydroxyvitamin D2 [1 alpha,24(S)-(OH)2D2]. 1 alpha-Hydroxyvitamin D3 incubated with the same cells gives rise to predominantly 25- and 27-hydroxylated products. Our identification of 1 alpha,24(S)-dihydroxyvitamin D2 is based on comparisons of the liver cell metabolite with chemically synthesized 1 alpha,24(S)-(OH)2D2 and 1 alpha,24(R)-(OH)2D2 by using HPLC, GC and GC-MS techniques. The stereochemical orientation of the 24-hydroxyl group was inferred after X-ray-crystallographic analysis of the 24(R)-OH epimer. 1 alpha,24(S)-Dihydroxyvitamin D2 binds strongly to the vitamin D receptor and is biologically active in growth hormone and chloramphenicol acetyltransferase reporter gene expression systems in vitro, but binds poorly to rat vitamin D-binding globulin, DBP. We suggest that this metabolite, 1 alpha,24(S)-(OH)2D2, possesses the spectrum of biological properties to be useful as a drug in the treatment of psoriasis, metabolic bone disease and cancer.
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