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xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-09 23:09:37
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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