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СÏÀ¼ÓÓÍľ³æ (СÓÐÃûÆø)
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΢Æ×ÇóÖúLF-85 ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (101 MHz, D2O) ¦Ä 20.3,21.8,22.3,23.7,26.7,28.9,30.8,46.0,60.0,60.7,61.2,62.3,69.1,69.5,70.4,71.0,71.1,71.3,71.6,72.1,72.3,72.5,73.0,73..1,73.9,74.1,74.3,75.7,75.8,76.3,76.9,81.3,92.1,95.8,103.6,180.6 |
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СÏÀ¼ÓÓÍ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-06 09:27:28
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1 . 2(2-¦Á-D-glucosyl)2isokestose ÏàËÆ¶È:66.6% Carbohydrate Research 2003 338 879-885 Synthesis and structural analysis of five novel oligosaccharides prepared by glucosyltransfer from ¦Â-d-glucose 1-phosphate to isokestose and nystose using Thermoanaerobacter brockii kojibiose phosphorylase Hideki Okada, Eri Fukushi, Shuichi Onodera, Tomoyuki Nishimoto, Jun Kawabata, Masanori Kikuchi, Norio Shiomi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2(2-¦Á-D-glucosyl)3isokestose ÏàËÆ¶È:66.6% Carbohydrate Research 2003 338 879-885 Synthesis and structural analysis of five novel oligosaccharides prepared by glucosyltransfer from ¦Â-d-glucose 1-phosphate to isokestose and nystose using Thermoanaerobacter brockii kojibiose phosphorylase Hideki Okada, Eri Fukushi, Shuichi Onodera, Tomoyuki Nishimoto, Jun Kawabata, Masanori Kikuchi, Norio Shiomi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 9¦Â-D-Galp-(1¡ú4)-¦Â-D-Galp-(1¡ú4)-¦Â-D-Galp-(1¡ú4)-D-GlcpNAc ÏàËÆ¶È:66.6% European Food Research and Technology 2010 231 55-63 Synthesis of oligosaccharides with lactose and N-acetylglucosamine as substrates by using b-D-galactosidase from Bacillus circulans Wei Li, Yi Sun, Hong Ye, Xiaoxiong Zeng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Tetrasaccharide ÏàËÆ¶È:65.7% Journal of the Chemical Society, Perkin Transactions 1 1996 1921-1926 Glycosidase-catalysed oligosaccharide synthesis of di-, tri- and tetra-saccharides using the N-acetylhexosaminidase from Aspergillus oryzae and the ¦Â-galactosidase from Bacillus circulans Suddham Singh, Michaela Scigelova, Gabin Vic and David H. G. Crout Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . LG-1 ÏàËÆ¶È:64.8% European Journal of Organic Chemistry 1995 1995 545-550 Biologically active glycosides from asteroidea, XXXII. Glycosphingolipids from the starfish Astropecten latespinosus, 2. Structure of two new ganglioside molecular species and biological activity of the ganglioside Ryuichi Higuchi, Shuji Matsumoto, Masanori Fujita, Tetsuya Komori and Takuma Sasaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2(2-¦Á-D-glucosyl)2nystose ÏàËÆ¶È:63.8% Carbohydrate Research 2003 338 879-885 Synthesis and structural analysis of five novel oligosaccharides prepared by glucosyltransfer from ¦Â-d-glucose 1-phosphate to isokestose and nystose using Thermoanaerobacter brockii kojibiose phosphorylase Hideki Okada, Eri Fukushi, Shuichi Onodera, Tomoyuki Nishimoto, Jun Kawabata, Masanori Kikuchi, Norio Shiomi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . decaisoside B C59H96O26 ÏàËÆ¶È:63.6% Phytochemistry 1993 33 427-430 Triterpenoid glycosides from Decaisnea fargesii Kong Jie, Li Xing-Cong, Wei Bi-Yu, Yang Chong-Ren Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . O-¦Â-D-fructofuranosyl-(2¡ú6)-O-¦Â-D-glucopyranosyl-(1¡ú3)-D-glucopyranose ÏàËÆ¶È:63.6% Chemistry Central Journal 2009 3 8 Structural analysis of three novel trisaccharides isolated from the fermented beverage of plant extracts Hideki Okada, Eri Fukushi, Akira Yamamori, Naoki Kawazoe, Shuichi Onodera, Jun Kawabata and Norio Shiomi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . O-Deacetylated polysaccharide ÏàËÆ¶È:63.6% Russian Journal of Bioorganic Chemistry 2008 34 460-467 Antigenic Polysaccharides of Bacteria: 41.1Structures of the O-Specific Polysaccharides of Shigella dysenteriae Types 4 and 5 Revised by NMR Spectroscopy A. V. Perepelov, S. N. Senchenkova, A. S. Shashkov, Yu. A. Knirel, B. Liu, L. Feng, and L. Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . decaisoside B ÏàËÆ¶È:63.6% Journal of Northwest Normal University (Natural Science) 1996 32 108-111 Chemical constituents and medical activity from Decaisnea Kong Jie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . propyl 2-acetamido-2-deoxy-3-O-(¦Á-L-fucopyranosyl)-4-O-{3-O-[2-acetamido-2-deoxy-3-O-(¦Á-L-fucopyranosyl)-4-O-(¦Â-D-galactopyranosyl)-¦Â-D-glucopyranosyl]-¦Â-D-galactopyranosyl}-¦Â-D-glucopyranoside C43H74N2O29 ÏàËÆ¶È:61.7% European Journal of Organic Chemistry 2011 6864-6876 Convergent Preparation of DimLex Hexasaccharide Analogues Jenifer L. Hendel and France-Isabelle Auzanneau Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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