Studies on the Conformational Aspects of Inulin Oligomers

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Abstract

The conformational studies of inulin oligomers from G-F2 to G-F9, which isolated from Platycodon grandiflorum, suggested a plausible conformational change between G-F7 and G-F8 from the trends in their chemical shift patterns and molecular rotation; the oligomers higher than G-F8 would form some secondary conformations more rigid than shorter oligomers. On the other hand, spin-lattice relaxation (7) studies of the protons proposed through-space interactions of 2- and 4-H's of glucose moiety in G-F5, presumably with some atom(s) of the terminal fructose moiety. This would reflect that the inulin molecule adopts a 5/1 helix. © 1992, The Pharmaceutical Society of Japan. All rights reserved.

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Oka, M., Ota, N., Mino, Y., Iwashita, T., & Komura, H. (1992). Studies on the Conformational Aspects of Inulin Oligomers. Chemical and Pharmaceutical Bulletin, 40(5), 1203–1207. https://doi.org/10.1248/cpb.40.1203

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