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1 .     tremulacin
C27H28O11     ÏàËÆ¶È:96.1%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     tremulacin
C27H28O11     ÏàËÆ¶È:88.4%
Journal of Natural Products          2006          69          1300-1304
Dovyalicin-Type Spermidine Alkaloids from Dovyalis Species
Bonnie Rasmussen, Aimee-Justine Nkurunziza, Matthias Witt, Hellen A. Oketch-Rabah,Jerzy W. Jaroszewski and Dan Stærk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     tremulacin
    ÏàËÆ¶È:88.4%
Journal of Natural Products          1991          Vol 54          1447
Chaenomeloidin: A Phenolic Glucoside from Leaves of Salix chaenomeloides
Mizuo Mizuno, Masaya Kato, Chiemi Misu, Munekazu Iinuma, Toshiyuki Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     tremulacin
    ÏàËÆ¶È:84.6%
Acta Pharmaceutica Sinica          1993          28          437-441
STUDIES ON THE CHEMICAL CONSTITUENTS OF POPULUS TOMENTOSA CARR
M Lin and SZ Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     salicyl tremuloidin
    ÏàËÆ¶È:73.0%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     cochinchiside B
C27H28O12     ÏàËÆ¶È:73.0%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     cochinchiside A
C27H28O11     ÏàËÆ¶È:69.2%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     tremulacinol epimer
    ÏàËÆ¶È:69.2%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     tremulacinol
C27H30O11     ÏàËÆ¶È:65.3%
Journal of Natural Products          2004          67          659-663
Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities
Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     demethylapollinin 7-O-¦Â‑D-glucopyranoside
C27H26O10     ÏàËÆ¶È:62.9%
Planta Medica          2011          77          1861-1864
Profiling of Phenolics from Tephrosia cinerea
Maldini, Mariateresa; Montoro, Paola; Macchia, Mario; Pizza, Cosimo; Piacente, Sonia:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     salicyloyltremuloidin
    ÏàËÆ¶È:61.5%
Journal of Natural Products          1991          Vol 54          1447
Chaenomeloidin: A Phenolic Glucoside from Leaves of Salix chaenomeloides
Mizuo Mizuno, Masaya Kato, Chiemi Misu, Munekazu Iinuma, Toshiyuki Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2'-O-acetylsalicortin
C22H26O11     ÏàËÆ¶È:61.5%
Journal of Natural Products          1992          Vol 55          970
Phenolic Glycosides from Salix lasiandra
Paul B. Reichardt, Howard M. Merken, Thomas P. Clausen, Jiejun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     6-O-[(6''-O-allophanyl)-¦Â-D-glucopyranosyl]-2,5-dihydroxy-7-phenylphenalen-1-one
    ÏàËÆ¶È:61.5%
Phytochemistry          2013          91          165-176
Biosynthesis of tetraoxygenated phenylphenalenones in Wachendorfia thyrsiflora
Tobias Munde, Silke Brand, William Hidalgo, Ravi K. Maddula, Aleš Svatoš, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     6-O-[(6''-Oallophanyl)-¦Â-D-glucopyranosyl]-2,5-dihydroxy-7-phenylphenalen-1-one
C27H24N2O11     ÏàËÆ¶È:59.2%
Journal of Natural Products          2002          65          1122-1130
Phenylphenalenone-Related Compounds: Chemotaxonomic Markers of the Haemodoraceae from Xiphidium caeruleum
Stefan Opitz, Dirk Hölscher, Neil J. Oldham, Stefan Bartram, and Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (4S,5S)-4-(2-anilinocarbonylpyrrolidin-1-ylcarbonyl)-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole
C31H27N3O3     ÏàËÆ¶È:59.2%
Heterocycles          2010          82          603-617
Diastereoselective Cyclization Reactions of Chiral Proline Auxiliary-Substituted N-Benzoyl-¦Á-dehydro(1-naphthyl)alaninamide Derivatives via Photoinduced Electron Transfer
Yuhki Sato, Yuhta Haruyama, Tetsutaro Igarashi, and Tadamitsu Sakurai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Marinoid E
C27H32O12     ÏàËÆ¶È:59.2%
Magnetic Resonance in Chemistry          2008          46          638-642
Structure elucidation of five new iridoid glucosides from the leaves of Avicennia marina (pages 638¨C642)
Yu Sun, Jie Ouyang, Zhiwei Deng, Qingshan Li and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     lasiandrin
C29H32O14     ÏàËÆ¶È:58.6%
Journal of Natural Products          1992          Vol 55          970
Phenolic Glycosides from Salix lasiandra
Paul B. Reichardt, Howard M. Merken, Thomas P. Clausen, Jiejun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     5-(Methoxycarbonyl)pentyl 3,4-di-O-benzoyl-2-O-methyl-¦Á-L-fucopyranosyl-(1¡ú2)-4-O-methyl-¦Â-Dgalactopyranoside
C35H46O14     ÏàËÆ¶È:58.0%
Molecules          2012          17          9023-9042
Synthesis, Antigenicity Against Human Sera and Structure-Activity Relationships of Carbohydrate Moieties from Toxocara larvae and Their Analogues
Akihiko Koizumi, Kimiaki Yamano, Takashi Tsuchiya, Frank Schweizer, Fumiyuki Kiuchi and Noriyasu Hada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     10-O-benzoyl-10-O-deacetyldaphylloside
C24H28O12     ÏàËÆ¶È:57.6%
Helvetica Chimica Acta          2006          Vol. 89          884
Study on the Chemical Constituents of Daphniphyllum angustifolium
Haiyun Bai and Lihong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     eucomoside B
C25H31NO11     ÏàËÆ¶È:57.6%
Journal of Natural Products          2007          70          1312-1316
Iridoids from the Green Leaves of Eucommia ulmoides
Chika Takamura,Tetsuya Hirata,Taro Ueda, Masateru Ono, Hiroyuki Miyashita, Tsuyoshi Ikeda, and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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