Record number :
1306229
Title of article :
‘Novel alkyl side chain sulfone 1α,25-dihydroxyvitamin D3 analogs: A comparison of in vitro antiproliferative activities and in vivo calcemic activities’ Original Research Article
Author/Authors :
Aimee R. Usera، نويسنده , , Patrick Dolan، نويسنده , , Thomas W. Kensler، نويسنده , , Gary H. Posner، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
5
From page :
5627
To page :
5631
Abstract :
The replacement of a t-butyl group with a trifluoromethyl group has profound effects on the biological profile of 1α,25-dihydroxyvitamin D3 sulfone analogs. Investigation of whether the improved biological activities are due to steric and electronic factors of the trifluoromethyl group led to the design, synthesis and biological evaluation of two analogous alkyl sulfone molecules, methyl sulfone (AU-16-ene-25-SO2–CH3) and isopropyl sulfone (AU-16-ene-25-SO2–i-Pr). These alkyl sulfones are sterically comparable to, but electronically very different from a trifluoromethyl group. The syntheses, antiproliferative activities and calcemic activities of these new alkyl sulfones are presented herein. In comparing the in vitro antiproliferative profiles of the new alkyl sulfone 1α,25-dihydroxyvitamin D3 analogs with the trifluoromethylsulfone and an analogous t-butyl sulfone, the activities increase in the following order: CH3
Keywords :
1? , Sulfone , Calcitriol , Trifluoromethyl , Antiproliferative , 25-Dihydroxyvitamin D3
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2009
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