Literature DB >> 28716761

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

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.
Copyright © 2017 Elsevier Ltd. All rights reserved.

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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


  1 in total

1.  The First Convergent Synthesis of 23,23-Difluoro-25-hydroxyvitamin D3 and Its 24-Hydroxy Derivatives: Preliminary Assessment of Biological Activities.

Authors:  Sayuri Mototani; Fumihiro Kawagoe; Kaori Yasuda; Hiroki Mano; Toshiyuki Sakaki; Atsushi Kittaka
Journal:  Molecules       Date:  2022-08-22       Impact factor: 4.927

  1 in total

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