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1 .     3,9-dihydroxymegastigmast-5-ene-3-O-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:76%
Journal of Agricultural and Food Chemistry          2006          54          9592-9597
Spectroscopic Identification and Antioxidant Activity of Glucosylated Carotenoid Metabolites from Cydonia vulgaris Fruits
Antonio Fiorentino, Brigida D'Abrosca, Severina Pacifico, Claudio Mastellone, Vincenzo Piscopo, and Pietro Monaco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (3R,9S)-megastigman-5-en-3,9-diol 3-O-[¦Á-L-arabinofuranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
C24H42O11     ÏàËÆ¶È:72%
Chemical & Pharmaceutical Bulletin          2005          53(7)          783-787
A Monoterpene Glucoside and Three Megastigmane Glycosides from Juniperus communis var. depressa
Tsutomu NAKANISHI,Naoki IIDA,Yuka INATOMI,Hiroko MURATA,Akira INADA,Jin MURATA,Frank A. LANG,Munekazu IINUMA,Toshiyuki TANAKA,and Yoshikazu SAKAGAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     staphylionoside K
C25H44O12     ÏàËÆ¶È:72%
Chemical & Pharmaceutical Bulletin          2005          53(7)          800-807
Staphylionosides A¡ªK: Megastigmane Glucosides from the Leaves of Staphylea bumalda DC.
Qian YU,Katsuyoshi MATSUNAMI,Hideaki OTSUKA,and Yoshio TAKEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     myrsinionoside E
C24H42O11     ÏàËÆ¶È:72%
Chemical & Pharmaceutical Bulletin          2001          49(12)          1558-1566
Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma
Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ficalloside
C24H42O11     ÏàËÆ¶È:72%
Natural Product Communications          2011          6          159-162
Chemical Constituents and Antioxidant Activity of Ficus callosa
Phan Van Kiem, Nguyen Xuan Cuong, Nguyen Xuan Nhiem, Dan Thi Thuy Hang, Nguyen Hoai Nam, Ninh Khac Ban, Chau Van Minh, Zhou Bing, Hae Dong Jang and Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     staphylionoside K
    ÏàËÆ¶È:72%
Acta Pharmaceutica Sinica          2010          45          1527-1532
Two new phenolic glycosides from the stems of Clematis parviloba
YAN Li-hua, XU Li-zhen *, WANG Zhi-min, ZHANG Qi-wei, YANG Shi-lin *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     foliasalacioside E2
C24H42O11     ÏàËÆ¶È:68%
Chemical & Pharmaceutical Bulletin          2008          56(4)          547-553
Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis
Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     foliasalacioside E3
C24H42O11     ÏàËÆ¶È:68%
Chemical & Pharmaceutical Bulletin          2008          56(4)          547-553
Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis
Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     foliasalacioside F
C24H42O11     ÏàËÆ¶È:68%
Chemical & Pharmaceutical Bulletin          2008          56(4)          547-553
Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis
Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     platanionoside H
C24H42H11     ÏàËÆ¶È:68%
Chemical & Pharmaceutical Bulletin          2002          50(3)          390-394
Platanionosides D¡ªJ: Megastigmane Glycosides from the Leaves of Alangium platanifolium (SIEB. et ZUCC.) HARMS var. platanifolium SIEB. et ZUCC.
Hideaki OTSUKA and Akie TAMAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     foliasalacioside E1
C24H42O11     ÏàËÆ¶È:64%
Chemical & Pharmaceutical Bulletin          2008          56(4)          547-553
Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis
Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     foliasalacioside I
C24H42O11     ÏàËÆ¶È:64%
Chemical & Pharmaceutical Bulletin          2008          56(4)          547-553
Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis
Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Linarionoside C
C25H44O12     ÏàËÆ¶È:64%
Phytochemistry          1994          37          461-465
Linarionosides A¨CC and acyclic monoterpene diglucosides from Linaria japonica
Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     linarionoside C
    ÏàËÆ¶È:64%
Acta Pharmaceutica Sinica          2010          45          1527-1532
Two new phenolic glycosides from the stems of Clematis parviloba
YAN Li-hua, XU Li-zhen *, WANG Zhi-min, ZHANG Qi-wei, YANG Shi-lin *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     2¦Â,3¦Â,20R,22R,25-Pentahydroxy-5¦Â-cholest-6,8(14)-dien
C27H44O5     ÏàËÆ¶È:59.2%
Steroids          2007          72          751-755
Three new steroids from the roots of Serratula wolffii
Andr¨¢s Simon, G¨¢bor T¨®th, Erika Liktor-Busa, Zolt¨¢n Kele, M¨¢ria Tak¨¢cs, Andr¨¢s Gergely, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (2¦Â,3¦Á,5¦Â,14¦Â,22R)- 2,3,20,22,25-pentahydroxycholest-7-en-6-one
C27H44O6     ÏàËÆ¶È:57.6%
Helvetica Chimica Acta          2008          Vol. 91          1640
Additional Minor Phytoecdysteroids of Serratula wolffii
Andr¨¢s Simon, Erika Liktor-Busa, G¨¢bor To´ th, Zolt¨¢n Kele, Judit Groska, and M¨¢ria B¨¢thori¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ent-14-labden-8¦Â,13¦Á-diol 19-O-¦Â-D-glucopyranoside
C26H46O8     ÏàËÆ¶È:57.6%
Journal of Natural Products          2007          70          1837-1845
Diterpenoid Glycosides from the Bitter Fern Gleichenia quadripartita
Cecilia Socolsky,Yoshinori Asakawa,and Alicia Bard¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     hymatoxin K
C26H40O9     ÏàËÆ¶È:57.6%
Natural Product Research          1995          6          37-42
Hymatoxins K and L, Novel Phytotoxins from Hypoxylon mammatum, Fungal Pathogen of Aspens
Akino Jossang; Bodnem Mbeminack; Jean Pinon; Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     gomojoside K
C26H44O8     ÏàËÆ¶È:57.6%
Phytochemistry          1993          32          1515-1518
Diterpene glucosides from Viburnum suspensum
Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     gomojoside L
C26H46O8     ÏàËÆ¶È:57.6%
Phytochemistry          1993          32          1515-1518
Diterpene glucosides from Viburnum suspensum
Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     gomojoside Q
C26H42O8     ÏàËÆ¶È:57.6%
Phytochemistry          1993          32          1515-1518
Diterpene glucosides from Viburnum suspensum
Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (4R,13S)-18-O-¦Â-Dglucopyranosyllabda-8(17),14-dien-13-ol
C26H44O7     ÏàËÆ¶È:57.6%
Helvetica Chimica Acta          2011          94          1085-1090
Diterpenoids from Diplopterygium rufopilosum
Jiang Hu, Xuan-Qin Chen, and Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     2¦Â,15S,16,17,19-pentahydroxy-isopimar-8(14)-ene 17-O-¦Â-D-glucopyranoside
C26H44O10     ÏàËÆ¶È:57.6%
Phytochemistry          2012          76          172-177
Diterpenes,ionol-derived,and flavone glycosides from Podocarpus elongatus
Laura Faiella,Abeer Temraz,Nunziatina De Tommasi,Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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