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²éѯ½á¹û£º¹²²éµ½276¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6,7-dihydroxy-dihydrolinalool 3-O-¦Â-glucopyranoside C16H30O8 ÏàËÆ¶È:82.3% Phytochemistry 2000 53 937-940 Monoterpene and pregnane glucosides from Solenostemma argel M.S. Kamel, K. Ohtani, H.A. Hasanain, M.H. Mohamed, R. Kasai, K. Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,7-dimethyloct-1-ene-3,6,7-triol 3-O-¦Â-D-glucopyranoside C16H30O8 ÏàËÆ¶È:76.4% Chemical & Pharmaceutical Bulletin 1999 47 639-642 Monoterpenoid Glucosides of Cnidium monnieri Fruit Junichi KITAJIMA,Yoshie AOKI,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S,6R)-6,7-dihydroxy-6,7-dihydrolinalool 3-O-¦Â-D-(3-O-potassium sulfo)-glucopyranoside C16H29KO11S ÏàËÆ¶È:76.4% Chemical & Pharmaceutical Bulletin 2003 51 32-39 Water-Soluble Constituents of Coriander Toru Ishikawa, Kyoko Kondo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (3S,6S)-6,7-dihydroxy-6,7-dihydrolinalool 3-O-¦Â-D-glucopyranoside C16H30O8 ÏàËÆ¶È:70.5% Chemical & Pharmaceutical Bulletin 2003 51 32-39 Water-Soluble Constituents of Coriander Toru Ishikawa, Kyoko Kondo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . trans-Linalool-3,6-oxide-¦Â-D-glucopyranoside C16H28O7 ÏàËÆ¶È:70.5% Planta Medica 2012 78 1574-1578 New Monoterpenes, Diterpenes, and Lignans from Abies recurvata Li, Yong-Li; Zhang, Ji-Gang; Yu, Ping; Ke, Bei-Lei; Ye, Ji; Yang, Xian-Wen; Jin, Hui-Zi; Zhang, Wei-Dong: Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compoud 17 C17H28O8 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 1995 43 729-733 Structure Elucidation of Six Acylated Iridoid Glucosides from Jasminum hemsleyi Takao TANAHASHI,Atsuko SHIMADA,Naotaka NAGAKURA,Kenichiro INOUE,Masami ONO,Tetsuro FUJITA and Cheng-Chang CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . trans-p-menthane-1,7,8-triol 8-O-¦Â-D-glucopyranoside C16H30O7 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 1998 46 1603-1606 Water-Soluble Constituents of Fennel. IV. Menthane-Type Monoterpenoids and Their Glycosides Toru ISHIKAWA,Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (6R)-menthiafolic acid 6-O-¦Â-D-quinovoside C16H26O7 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 1997 45 807-812 Acacia concinna Saponins. II. Structures of Monoterpenoid Glycosides in the Alkaline Hydrolysate of the Saponin Fraction Fumiyuki KIUCHI,Md.Abdul GAFUR,Tohoru OBATA,Akiko TACHIBANA and Yoshisuke TSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3(S)-linalyl-¦Â-D-glucopyranoside C16H28O6 ÏàËÆ¶È:64.7% Phytochemistry 1994 36 1435-1437 Linalyl ¦Â-D-glucopyranoside and its 6¡ä-O-malonate as aroma precursors from Jasminum sambac Jae-Hak Moon, Naoharu Watanabe, Kanzo Sakata, Junji Inagaki, Akihito Yagi, Kazuo Ina, Shaojun Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . linalyl ¦Â-D-glucopyranoside ÏàËÆ¶È:64.7% Phytochemistry 1994 37 543-546 A phenylpropanoid glucoside from Perilla frutescens Tomoyuki Fujita, Atsunori Funayoshi, Mitsuru Nakayama Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (3S,6R)-6,7-dihydroxy-6,7-dihydrolinalool 3-O-¦Â-D-glucopyranoside C16H30O8 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 2003 51 32-39 Water-Soluble Constituents of Coriander Toru Ishikawa, Kyoko Kondo and Junichi Kitajima Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . linaloyl glucoside C16H28O6 ÏàËÆ¶È:64.7% Phytochemistry 1989 28 3369-3372 Terpenic glycosides from Pluchea indica Taketo Uchiyama,Toshio Miyase,Akira Ueno,Khan Usmanghani Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (3S)-3-O-(¦Â-D-Glucopyranosyl)-3,7-dimethylocta-1,5-dien-3-ol C16H28O6 ÏàËÆ¶È:64.7% Bulletin of the Korean Chemical Society 2003 24 1475-1477 A New Monoterpene Glucoside from Portulaca oleracea Youngwan Seo, Jongheon Shin, Hyo Jun Cha, You-Ah Kim, Jong-Woong Ahn, Burm-Jong Lee, Dong Seok Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (3R)-linaloyl ¦Â-D-glucopyranoside C16H28O6 ÏàËÆ¶È:64.7% Carbohydrate Research 1997 301 123-143 First total synthesis of two new diglycosides, neohancosides A and B, from Cynanchum hancockianum Yaeko Konda, Tsuneyuki Toida, Eisuke Kaji, Kazuyoshi Takeda, Yoshihiro Harigaya Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (3S)-linaloyl ¦Â-D-glucopyranoside C16H28O6 ÏàËÆ¶È:64.7% Carbohydrate Research 1997 301 123-143 First total synthesis of two new diglycosides, neohancosides A and B, from Cynanchum hancockianum Yaeko Konda, Tsuneyuki Toida, Eisuke Kaji, Kazuyoshi Takeda, Yoshihiro Harigaya Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . lipedoside B-IV C22H40O12 ÏàËÆ¶È:63.6% Phytochemistry 1994 36 709-716 Monoterpenoid and phenylethanoid glycosides from Ligustrum pedunculare Zheng-Dan He, Shinichi Ueda, Masako Akaji, Tetsuro Fujita, Kenichiro Inoue, Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . lipedoside B-IV ÏàËÆ¶È:63.6% Chemistry & Biodiversity 2013 10 96-128 Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum Bei-Bei Gao, Gai-Mei She and Dong-Mei She Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . icariside C3 C21H38O8 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1987 35 1109-1117 Studies on the Glycosides of Epimedium grandiflorum MORR. Var. thunbergianum (MIQ.) NAKAI. I TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO KARASAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . schensianolside A C21H36O8 ÏàËÆ¶È:61.9% Chinese Chemical Letters 2009 20 952-954 Three new sesquiterpenes from Euonymus schensianus Maxim Xiao Ke Zheng, Jin Hui Guo, Wei Sheng Feng , Hong Wei Li Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (4R)-p-menth-1-ene-7,8-diol 8-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside C21H36O11 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1998 46 1595-1598 Monoterpenoid Glycosides of Glehnia littoralis Root and Rhizoma Junichi KITAJIMA,Chieko OKAMURA,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (4S)-p-menth-1-ene-7,8-diol 8-O-¦Â-D-apiofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside C21H36O11 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1998 46 1595-1598 Monoterpenoid Glycosides of Glehnia littoralis Root and Rhizoma Junichi KITAJIMA,Chieko OKAMURA,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . linaloyl apiosyl glucoside C21H36O10 ÏàËÆ¶È:61.9% Phytochemistry 1989 28 3369-3372 Terpenic glycosides from Pluchea indica Taketo Uchiyama,Toshio Miyase,Akira Ueno,Khan Usmanghani Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Amarantholidoside V C21H38O8 ÏàËÆ¶È:61.9% Tetrahedron 2006 62 8952-8958 Unusual sesquiterpene glucosides from Amaranthus retroflexus Antonio Fiorentino, Marina DellaGreca, Brigida D'Abrosca, Annunziata Golino, Severina Pacifico, Angelina Izzo, Pietro Monaco Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . pumilaside A C21H38O8 ÏàËÆ¶È:61.9% Chinese Journal of Pharmaceuticals 2010 41 823-826 Studies on Chemical Constituents of Celastrus orbiculatus ZHANG Yang, XU Haiyan, TAN Junjie, TAN Changheng, YANG Peiming Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . praeroside VI C20H26O10 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2008 56(9) 1349-1351 Studies of Coumarins from the Chinese Drug Qianhu, XXVII1):Structure of a New Simple Coumarin Glycoside from Bai-Hua Qianhu, Peucedanum praeruptorum Hirotaka ISHII,Yoshihito OKADA, Masaki BABA, and Toru OKUYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . devenyoside A C20H26O10 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 1637-1641 Coumarins from the Fruits of Seseli devenyense Jarek Widelski, Eleni Melliou, Nikolas Fokialakis, Prokopios Magiatis, Kazimierz Glowniak, and Ioanna Chinou Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . funingensin A ÏàËÆ¶È:60% Food Chemistry 2010 123 1123-1126 Eudesmane sesquiterpene glucosides from lychee seed and their cytotoxic activity Xinya Xu, Haihui Xie, Jing Hao, Yueming Jiang, Xiaoyi Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (2E,6S)-6-hydroxy-2-hydroxymethyl-6-methyl-2,7-octadienoic acid 6-O-¦Â-D-quinovopyranoside C16H26O8 ÏàËÆ¶È:58.8% Journal of Natural Products 2009 72 632-639 Cytotoxic Oleanane Triterpene Saponins from Albizia chinensis Rui Liu,Shuanggang Ma,Shishan Yu,Yuehu Pei, Sen Zhang,Xiaoguang Chen, and Jianjun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . sachalinoside B C16H28O7 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2001 49(4) 396-401 Prolyl Endopeptidase Inhibitors from the Underground Part of Rhodiola sachalinensis Wenzhe FAN,Yasuhiro TEZUKA,Khin May NI,and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 3,7-dimethyloct-1-ene-3,6,7-triol C15H30O8 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2000 48(7) 1090-1092 Conduritol F Glucosides and Terpenoid Glucosides from Cynanchum liukiuense and Distribution of Conduritol F Glucosides in Several Asclepiadaceous Plants Fumiko ABE and Tatsuo YAMAUCHI ,Keiichi HONDA,and Nanao HAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . monoterpene glycoside ÏàËÆ¶È:58.8% Journal of Natural Products 2008 71(1) 41-46 Cytotoxic Triterpenoid Saponins Acylated with Monoterpenic Acid from Pithecellobium lucidum Shuang Gang Ma, You Cai Hu, Shi Shan Yu, Yi Zhang, Xiao Guang Chen, Jing Liu, and Yu Xi Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 8a C16H26O8 ÏàËÆ¶È:58.8% Journal of Natural Products 2000 63 1658-1664 Kinmoonosides A-C, Three New Cytotoxic Saponins from the Fruits of Acacia concinna, a Medicinal Plant Collected in Myanmar Yasuhiro Tezuka, Kazuyuki Honda, Arjun H. Banskota, Maung Maung Thet, and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . compoud 16 C17H28O8 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 1995 43 729-733 Structure Elucidation of Six Acylated Iridoid Glucosides from Jasminum hemsleyi Takao TANAHASHI,Atsuko SHIMADA,Naotaka NAGAKURA,Kenichiro INOUE,Masami ONO,Tetsuro FUJITA and Cheng-Chang CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-19 09:44:16
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