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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 20.1,21.8,23.3,25.0,25.6,28.9,30.3,37.9,38.8,39.7,40.7,42.9,62.7,65.7,69.2,71.7,73.2,75.2,78.0,78.2,102.3,103.9,125.1,125.4,138.4 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½176¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |

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