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Recent developments for introducing a hexafluoroisopropanol unit into the Vitamin D side chain

Authors :
Fumihiro Kawagoe
Toru Sugiyama
Atsushi Kittaka
Motonari Uesugi
Source :
The Journal of Steroid Biochemistry and Molecular Biology. 177:250-254
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

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.

Details

ISSN :
09600760
Volume :
177
Database :
OpenAIRE
Journal :
The Journal of Steroid Biochemistry and Molecular Biology
Accession number :
edsair.doi.dedup.....713f0765722aea5ac12c53267f373f72
Full Text :
https://doi.org/10.1016/j.jsbmb.2017.07.008