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dc.contributor.authorCarillo, Kathleen D.en_US
dc.contributor.authorWu, Dannien_US
dc.contributor.authorLin, Su-Chingen_US
dc.contributor.authorTsai, Shen-Longen_US
dc.contributor.authorShie, Jiun-Jieen_US
dc.contributor.authorTzou, Der-Lii M.en_US
dc.date.accessioned2019-10-05T00:08:38Z-
dc.date.available2019-10-05T00:08:38Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn0039-128Xen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.steroids.2019.108429en_US
dc.identifier.urihttp://hdl.handle.net/11536/152784-
dc.description.abstractIn this work, we used high resolution NMR spectroscopy to investigate metal cation chelation by the steroidal drug 1,4-pregnadiene-11 beta,17 alpha,21-triol-3,20-dione (Prednisolone; abbreviated as Prd). Prd/MgCl2 and Prd/CaCl2 mixtures were prepared at eight different molar ratios. Using two-dimensional H-1/C-13 heteronuclear correlation spectroscopy, we were able to resolve most of the H-1 signals, except those at 1.4-1.55 ppm, where signals for H15 beta, H16 alpha and Me-19 are superimposed. The chelation sites were determined by the cation concentration-dependent C-13 signals. Both ring A and ring D of Prd were found to be involved in Mg2+ chelation, whereas only ring A was involved in Ca2+ chelation. The dihedral angles deduced from the (3)J(H)(-H) coupling constants indicated that ring D of Prd might undergo rather small, but different, distortions in the presence of Mg2+ and Ca2+. Additionally, using the continuous variation method, we deduced that the stoichiometric ratios of the Prd/Mg2+ and Prd/Ca2+ complexes were 1:1 and 2:1, respectively. All of the evidence led us to conclude that the Prd/Mg2+ and Prd/Ca2+ complexes are mediated by different chelating mechanisms.en_US
dc.language.isoen_USen_US
dc.subjectPrednisoloneen_US
dc.subjectNMRen_US
dc.subjectCation chelationen_US
dc.subjectConformational changeen_US
dc.subjectCalciumen_US
dc.subjectMagnesiumen_US
dc.titleMagnesium and calcium reveal different chelating effects in a steroid compound: A model study of prednisolone using NMR spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.steroids.2019.108429en_US
dc.identifier.journalSTEROIDSen_US
dc.citation.volume150en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000486110300005en_US
dc.citation.woscount0en_US
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