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1 . myrsinionoside E C24H42O11 ÏàËÆ¶È:70.8% 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 2 . guettardionoside C24H40O11 ÏàËÆ¶È:70.8% Journal of Natural Medicines 2011 65 364-369 A glycerol ¦Á-D-glucuronide and a megastigmane glycoside from the leaves of Guettarda speciosa L. Wen-Hu Cai ,Katsuyoshi Matsunami ,Hideaki Otsuka ,Takakazu Shinzato ,Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxy-¦Á-ionol 9-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside C24H40O11 ÏàËÆ¶È:70.8% Journal of Agricultural and Food Chemistry 1996 44 1676-1681 Constituents of Cydonia vulgaris: Isolation and Structure Elucidation of Four New Flavonol Glycosides and Nine New ¦Á-Ionol-Derived Glycosides Nunziatina De Tommasi, Sonia Piacente, Francesco De Simone, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . byzantionoside B 6'-O-¦Â-D-apiofuranoside ÏàËÆ¶È:70.8% Chemistry of Natural Compounds 2014 50 772-773 Megastigmans from Turpinia arguta Min Wu, Ping Wu, Xiaoyi Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (3R,9R)-3-hydroxy-7,8-dihydro-¦Â-ionyl 6-O-¦Â-D-apiofuranosyl-¦Â-D-glucopyranoside C24H42O11 ÏàËÆ¶È:70.8% Phytochemistry 2001 56 819-825 The (3R,9R)-3-hydroxy-7,8-dihydro-¦Â-ionol disaccharide glycoside is an aroma precursor in tea leaves Seung-Jin Ma, Naoharu Watanabe, Akihito Yagi, Kanzo Sakata Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . myrsinionoside E ÏàËÆ¶È:70.8% Chemical & Pharmaceutical Bulletin 2001 49 1093-1097 Myrsinionosides A-E: Megastigmane Glycosides from the Leaves of Myrsine seguinii LEV. Hideaki OTSUKA, Xi-Ning ZHONG, Eiji HIRATA, Takakazu SHINZATO, Yoshio TAKEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-oxo-¦Á-ionyl-9-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside C24H38O11 ÏàËÆ¶È:66.6% Journal of Natural Products 1992 Vol 55 1025 Plant Metabolites. New Sesquiterpene and Ionone Glycosides from Eriobotrya japonica Nunziatina De Tommasi, Rita Aquino, Francesco De Simone, Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ficalloside C24H42O11 ÏàËÆ¶È:66.6% 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 9 . 3-hydroxy-5,6-epoxy-¦Â-ionol -3-O-¦Â-apiofuranosyl-(1¡ú6)-hglucopyranoside C24H40O12 ÏàËÆ¶È:62.5% Fitoterapia 2004 75 785-788 A new diglycosyl megastigmane from Carallia brachiata S.-K. Ling, T. Takashima, T. Tanaka, T. Fujioka,K. Mihashi, I. Kouno Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . zansimuloside A ÏàËÆ¶È:62.5% Chinese Traditional and Herbal Drugs 2007 38 488-490 A new monoterpenoid glycoside from roots of Zanthoxylum simulans WU Jiao; MEI Wen-li; DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 6 C26H38O13 ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 2012 60 913-919 Sesquiterpene Lactone Glycosides from the Roots of Ferula varia Shin-ichiro Kurimoto, Kyoko Suzuki, Mamoru Okasaka, Yoshiki Kashiwada, Olimjion Kakhkharovich Kodzhimatov, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . galloyl Linarionoside A C26H38O11 ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 2014 62 185-190 Anti-inflammatory Compounds from the Aerial Parts of Aceriphyllum rossii Tran Thi Thu Trang, To Dao Cuong, Tran Manh Hung, Jeong Ah Kim, Jeong Hyung Lee, Mi Hee Woo, Jae Sue Choi, Hyeong Kyu Lee, Byung Sun Min Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . alangionoside B ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2008 Vol. 91 495 Three New Glycosides from the Stems of Miliusa balansae Yu Lei, Li-Jun Wu, Hai-Ming Shi, and Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . foliasalacioside E2 C24H42O11 ÏàËÆ¶È:58.3% 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 |

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