| Literature DB >> 28716761 |
Fumihiro Kawagoe1, Toru Sugiyama2, Motonari Uesugi3, Atsushi Kittaka4.
Abstract
Among numerous studies on synthetic approaches to and the biological activities of vitamin D analogues, we herein focused on falecalcitriol, an analogue of calcitriol (1α,25-dihydroxyvitamin D3), in which a 26,26,26,27,27,27-hexafluoroisopropanol unit has been introduced into the side chain. Falecalcitriol was designed to escape from the metabolism of CYP24A1 and has been used as a drug to treat secondary hyperparathyroidism since 2001. Its metabolite, the 23-hydroxy form, retains biological activity and resistants to further metabolism. Recent developments in synthetic methodologies for introducing the hexafluoroisopropanol unit into the vitamin D CD-ring side chain were described herein.Entities:
Keywords: CD-ring; Falecalcitriol; Hexafluoroacetone (HFA); Hexafluoroisopropanol unit; Ruppert-Prakash reagent (CF(3)TMS); Synthesis
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Year: 2017 PMID: 28716761 DOI: 10.1016/j.jsbmb.2017.07.008
Source DB: PubMed Journal: J Steroid Biochem Mol Biol ISSN: 0960-0760 Impact factor: 4.292