Fluorinated Vitamin D Analogs to Probe the Conformation of Vitamin D in Its Receptor Complex : ^<19>F-NMR Studies and Biological Activity

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To investigate vitamin D conformation, specifically the A-ring and seco-B ring parts, in its complex with the vitamin D receptor (VDR), we have previously suggested the use of ^<19>F-NMR spectroscopy and have synthesized three fluorovitamin D derivatives to be used for the study, 4,4-difluoro-1 α,25-dihydroxyvitamin D_3 [4,4-F_2 -1,25-(OH)_2 D_3, 2a], and (10Z)- and (10E)-19-fluoro-1 α,25-dihydroxyvitamin D_3 [19-F-1,25-(OH)_2D_3, 3a, 4a]. In this paper, we examined the ^<19>F-NMR spectra of these and related fluorovitamin D compounds in detail. In the low temperature ^<19>F-NMR spectra, we observed two well-separated rigid conformations of 2a (51 : 49) and 4a (84 : 16), while only one conformation was detected with 3a. The two observed conformers of 2a and 4a were respectively assigned to the known α- and β-conformers formed by the flipping of the A-ring where the C(19) exocyclic methylene points to the α- and β-faces. The single conformation observed for 3a was assigned to the α-conformer. We detected no other conformation in the ^<19>F-NMR of all vitamin D compounds examined. The effect of solvents on the ^<19>F chemical shifts of fluorovitamin D compounds was found to be small (less than 6.3 ppm). This was much smaller than the difference between the two A-ring conformers (13-30 ppm). Using the dynamic ^1studies of fluorovitamin D compounds, we determined the free energy of activation for the interconversion between the two conformations of 2a (9.9 kcal/mol) and 4a (10.8, 11.5 kcal/mol). Introduction of the 1α-hy-droxyl group raised the activation energy about 1 kcal/mol. The affinity for VDR was evaluated, and the relative potency of 2a, 3a and 4a was found to be 1%, 8% and 9%, respectively, of that of 1,25-(OH)_2 D_3 (1). Though the affinity for VDR was considerably reduced in these compounds, the ability to activate gene transcription was similar and remained in the range 30-50% of the effect of 1. This biological information in combination with the NMR properties indicates that 2a and 4a are promising probes for studying the VDR-bound A-ring conformation of vitamin D.
社団法人日本薬学会の論文
2002-04-01

Fluorinated Vitamin D Analogs to Probe the Conformation of Vitamin D in Its Receptor Complex : ^<19>F-NMR Studies and Biological Activity

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