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ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½31¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 5 ÏàËÆ¶È:60% Phytochemistry 1981 20 71-83 Iridoid mono- and di-glycosides in Mentzelia Søren Rosendal Jensen, Carl Bjarne Mikkelsen, Bent Juhl Nielsen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,6-O-isopropylidene-1,2,4-tri-O-methoxymethyl-D-gly-cero-D-galacto-heptitol C16H32O10 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2010 18 2829-2835 Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor Razieh Eskandari, Kumarasamy Jayakanthan, Douglas A. Kuntz, David R. Rose, B. Mario Pinto Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . epoxycerberidol-3-O-¦Â-D-glucoside C15H26O9 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1996 44 1797-1800 10-Carboxyloganin, Normonoterpenoid Gluosides and Dinormonoterpenoid Glucosides from the Leaves of Cerbera manghas(Studies on Cerbera. 10) Fumiko ABE and Tatsuo YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1984 32 4674-4677 STUDY OF RED GINSENG : NEW GLUCOSIDES AND A NOTE ON THE OCCURRENCE OF MALTOL Hiromichi Matsuura,Yuhzo Hirao,Susumu Yoshida,Kazuo Kunihiro,Tohru Fuwa,Ryoji Kasai and Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 8 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1984 32 4674-4677 STUDY OF RED GINSENG : NEW GLUCOSIDES AND A NOTE ON THE OCCURRENCE OF MALTOL Hiromichi Matsuura,Yuhzo Hirao,Susumu Yoshida,Kazuo Kunihiro,Tohru Fuwa,Ryoji Kasai and Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Stilbericoside hexaacetate ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1599-1603 Biosynthesis of iridoid glucosides inThunbergia alata Søren Damtoft, Lotte Boe Frederiksen, Søren Rosendal Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4,6-O-isopropylidene-1,2,3-tri-O-methoxymethyl-D-glycero-L-gulo-heptitol C16H32O10 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2011 19 2252-2262 Role of the side chain stereochemistry in the ¦Á-glucosidase inhibitory activity of kotalanol, a potent natural ¦Á-glucosidase inhibitor Weijia Xie, Genzoh Tanabe, Kanjyun Matsuoka, Mumen F. A. Amer, Toshie Minematsu,Xiaoming Wu, Masayuki Yoshikawa, Osamu Muraoka Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . physoside hexaacetate C27H36O16 ÏàËÆ¶È:53.3% Phytochemistry 1989 28 3047-3050 Glycerol tridehydrocrepenynate from the basidiomycete Craterellus cornucopioides Volker Magnus,Goran Laćan,Robin T. Aplin,Viktor Thaller Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . MethylO-¦Á-D-mannopyranosyl-(1¡ú2)-¦Á-D-galactopyranoside ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 1993 1 237-257 Synthesis of di- to penta-saccharides related to the O-specific polysaccharide of Shigella dysenteriae type 1, and their nuclear magnetic resonance study Vince Pozsgay, Bruce Coxon, Herman Yeh Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Á-D-gluco-hept-2-ulopyranose ¦Â-D-gluco-hept-2'-ulopyranose 1,2':2,1'-dianhydride C14H24O12 ÏàËÆ¶È:53.3% Tetrahedron 2001 57 8053-5066 Stereoselective synthesis and structure elucidation of spiro-ketodisaccharides Xiaoliu Li, Hideyo Takahashi, Hiro Ohtake, Moto Shiro, Shiro Ikegami Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-amino-3-deoxy-¦Á-D-allopyranosyl ¦Á-D-glucopyranoside ÏàËÆ¶È:53.3% The Journal of Antibiotics 1989 42 585-590 PREPARATION OF 3-AMINO-3-DEOXY DERIVATIVES OF TREHALOSE AND SUCROSE AND THEIR ACTIVITIES NAOKI ASANO, KATSUMI KATAYAMA, MASAYOSHI TAKEUCHI, TADASHI FURUMOTO, YUKIHIKO KAMEDA, KATSUHIKO MATSUI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . potassium (2R)-2-O-¦Á-D-Mannopyranosyl-(1 2)-¦Á-D-glucopyranosyl-2,3-dihydroxypropanoate C15H26O14 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2011 6698-6703 Synthesis of Potassium (2R)-2-O--D-Mannopyranosyl-(1¡ú2)--D-glucopyranosyl-2,3-dihydroxypropanoate: A Naturally Compatible Solute Eva C. Lourenço and M. Rita Ventura Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . bis(methyl 2-deoxy-¦Á-D-mannopyranosid-2-yl) sulfoxide C14H26O11S ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2010 1951-1970 Non-Glycosidically Linked Pseudodisaccharides: Thioethers, Sulfoxides, Sulfones, Ethers, Selenoethers, and Their Binding to Lectins Ian Cumpstey, Clinton Ramstadius, Tashfeen Akhtar, Irwin J. Goldstein and Harry C. Winter Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . xylaroside B C16H24O7 ÏàËÆ¶È:50% Phytochemistry 2008 69 1900-1902 Metabolites from the endophytic fungus Xylaria sp. PSU-D14 Wipapan Pongcharoen, Vatcharin Rukachaisirikul, Souwalak Phongpaichit, Till K¨¹hn, Matthias Pelzing, Jariya Sakayaroj, Walter C. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3,4-dihydro-methylcatalpol C16H26O10 ÏàËÆ¶È:50% Phytochemistry 2005 66 355-362 Anti-protozoal and plasmodial FabI enzyme inhibiting metabolites of Scrophularia lepidota roots Deniz Tasdemir, Nadide Deniz G¨¹ner, Remo Perozzo, Reto Brun,Ali A. Dönmez, Ihsan Çalis, Peter R¨¹edi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Pentaacetyl 6-¦Â-hydroxysweroside C26H32O15 ÏàËÆ¶È:50% Biochemical Systematics and Ecology 2002 30 243-247 An iridoid glucoside from Gronovia scandens (Loasaceae) Ver¨®nica Rodr¨ªguez, Jan Schripsema, Søren Rosendal Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . swertiamarin ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 1993 28 522-525 SWERTIAPUNIMARIN FROM SWERTIA PUNICEA HEMSL P Tan. YL Liu and CY Hou Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . eustomoside C16H22O11 ÏàËÆ¶È:50% Journal of Natural Products 1980 Vol 43 649-707 Iridoids. A Review Leticia J. El-Naggar, Jack L. Beal Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . swertiamarin C16H22O11 ÏàËÆ¶È:50% Journal of Natural Products 1980 Vol 43 649-707 Iridoids. A Review Leticia J. El-Naggar, Jack L. Beal Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . lamiol ÏàËÆ¶È:50% Journal of Natural Products 1983 Vol 46 157-160 6-Deoxylamioside, A New Iridoid Glucoside From Lamium amplexicaule Marcella Guiso, Carmela Martino Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5-O-Allosylantirrinoside ÏàËÆ¶È:50% Phytochemistry 1993 32 1068-1070 5-O-Allosylantirrinoside from Linaria species Emilia Ilieva, Nedjalka Handjieva, Stefan Spassov, Simeon Popov Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Tetra acety1 swertiamaroside ÏàËÆ¶È:50% Phytochemistry 1977 16 723-726 Feretoside et gardenoside du Feretia apodanthera: rmn du carbone 13 en s¨¦rie iridoide François Bailleul, Pierre Delaveau, Alain Rabaron, Michel Plat, Michel Koch Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . eustomoside tetraacetate ÏàËÆ¶È:50% Phytochemistry 1979 18 1981-1986 Three new secoiridoid glucosides from Eustoma russellianum Shinichi Uesato, Toshihiro Hashimoto, Hiroyuki Inouye Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . swertiamarin tetraacetate ÏàËÆ¶È:50% Phytochemistry 1979 18 1981-1986 Three new secoiridoid glucosides from Eustoma russellianum Shinichi Uesato, Toshihiro Hashimoto, Hiroyuki Inouye Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 4 C16H24O10 ÏàËÆ¶È:50% Phytochemistry 1984 23 121-123 Iridoid glucosides from Satureja Vulgaris Armandodoriano Bianco, Silvana Lamesi, Pietro Passacantilli Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 1 ÏàËÆ¶È:50% Phytochemistry 1984 23 121-123 Iridoid glucosides from Satureja Vulgaris Armandodoriano Bianco, Silvana Lamesi, Pietro Passacantilli Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 2,5-O-isopropylidene-4,6,7-tri-O-methoxymethyl-D-glycero-D-manno-heptitol C16H32O10 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 2829-2835 Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor Razieh Eskandari, Kumarasamy Jayakanthan, Douglas A. Kuntz, David R. Rose, B. Mario Pinto Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-09 23:05:10
gzl9901
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