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1 . 2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester C36H58O10 ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 2004 52(1) 157-159 A New Pentacyclic Triterpenoid Glucoside from Prunus serrulata var. spontanea Hyun Ah JUNG,Hae Young CHUNG,Jee H. JUNG,and Jae Sue CHOI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (2¦Â,3¦Á)-2,3,20,23,24,30-hexahydroxyurs-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester C36H58O13 ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2008 Vol. 91 575 Two New Polyoxygenated Triterpenoids from Actinidia valvata Hai-Liang Xin, Xiao-Qiang Yue, Yan-Feng Xu, Ying-Chun Wu, Ya-Ni Zhang, Yong-Zi Wang, and Chang-Quan Ling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester C36H58O11 ÏàËÆ¶È:77.7% Chemical & Pharmaceutical Bulletin 2004 52(1) 157-159 A New Pentacyclic Triterpenoid Glucoside from Prunus serrulata var. spontanea Hyun Ah JUNG,Hae Young CHUNG,Jee H. JUNG,and Jae Sue CHOI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2¦Á,3¦Â,23-trihydroxyurs-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:77.7% Acta Pharmaceutica Sinica 2006 Vol 41 835-839 A new triterpenoid saponin from stems of Akebia trifoliata GAO Hui-min; WANG Zhi-min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . vulgarsaponin A ÏàËÆ¶È:77.7% Acta Pharmaceutica Sinica 2000 Vol 35 29-31 STRUCTURE IDENTIFICATION OF VULGARSAPONIN A Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid ¦Â-D-glucopyranosyl ester ÏàËÆ¶È:77.7% Journal of Natural Medicines 2009 63 318-322 A new diterpenoid and a new triterpenoid glucosyl ester from the leaves of Callicarpa japonica Thunb. var. luxurians Rehd. Masateru Ono, Tomoyo Chikuba, Kenji Mishima, Toru Yamasaki and Tsuyoshi Ikeda, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid 28-O-¦Â-Dglucopyranoside ÏàËÆ¶È:77.7% Fitoterapia 2010 81 920-924 Two new triterpenoids from the roots of Actinidia chinensis Yi-Xin Xu, Zhao-Bao Xiang, Yong-Sheng Jin, Yang Shen, Hai-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . cincholic acid 28-O-¦Â-glucopyranosyl ester C36H56O10 ÏàËÆ¶È:75% Planta Medica 2005 71 355-361 Six New Triterpenoid Saponins from the Root and Stem Bark of Cephalanthus occidentalis Zhang, Zhizhen; Li, Shiyou; Zhang, Shanmin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Quadranoside IV ÏàËÆ¶È:75% Molecules 2008 13 2717-2728 Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 2¦Á,3¦Á,24-trihydroxyursa-12,20(30)-dien-28-oic acid ÏàËÆ¶È:75% Journal of Chinese Pharmaceutical Sciences 2000 9 128-130 A New Phenylpropanoid and Triterpenoids from Prunella vulgaris Wang Zhuju, Zhao Yuying, Wang Bin, Li Jiexiu, Ai Tiemin and Chen Yayan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester C36H58O11 ÏàËÆ¶È:75% Phytochemistry 1998 49 2477-2481 Pentacyclic triterpenoids from Rubus xanthocarpus Bao-Zhi Li, Bin-Gui Wang, Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2¦Á,3¦Á,19¦Á,23-tetrahydroxy-ursa-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2010 35 3297-3301 Chemical constituents from Callicarpa nudiflora and their hemostatic acitivity ZHANG Jie; LI Baoquan; FENG Feng; TANG Yuping; LIU Wenyuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2¦Á,3¦Á,23-trihydroxy-urs-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C36H58O10 ÏàËÆ¶È:75% Bioorganic & Medicinal Chemistry Letters 2012 22 2079-2083 Cytotoxic terpenoids from Juglans sinensis leaves and twigs Heejung Yang, Hyun-Jong Cho, So Hee Sim, Young Keun Chung, Dae-Duk Kim, Sang Hyun Sung, Jinwoong Kim, Young Choong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3¦Â,23-Dihydroxyurs-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C36H58O9 ÏàËÆ¶È:75% Journal of Natural Products 2011 74 751-756 Antiproliferative Triterpenes from the Leaves and Twigs of Juglans sinensis on HSC-T6 Cells Heejung Yang, Eun Ju Jeong, Jinwoong Kim, Sang Hyun Sung, and Young Choong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . callianthaside A C36H58O11 ÏàËÆ¶È:72.2% Helvetica Chimica Acta 2007 Vol. 90 2421 Phenolic and Triterpenoid Glycosides from Pyrola calliantha Yi-Lei Chen, Chang-Heng Tan, Jun-Jie Tan, Shi-Jin Qu, Heng-Bin Wang, Qiang Zhang, Shan-Hao Jiang, and Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . rubuside E C36H56O9 ÏàËÆ¶È:72.2% Journal of Natural Products 2009 72 1755-1760 Triterpenoid Saponins from Rubus ellipticus var. obcordatus Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . rubuside H C36H56O10 ÏàËÆ¶È:72.2% Journal of Natural Products 2009 72 1755-1760 Triterpenoid Saponins from Rubus ellipticus var. obcordatus Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (20S)-niga-ichigoside F1 C36H58O11 ÏàËÆ¶È:72.2% Journal of Natural Products 2005 68 1531-1535 Phenolic and Triterpene Glycosides from the Stems of Ilex litseaefolia Ai-Lian Zhang, Qi Ye, Bo-Gang Li, Hua-Yi Qi, and Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . quadranoside IV C36H58O10 ÏàËÆ¶È:72.2% Journal of Natural Products 2000 63 496-500 Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ¦Â-D-glucopyranosyl 2¦Á,3¦Â,23,24-tetrahydroxyurs-12-en-28-oate ÏàËÆ¶È:72.2% Molecules 2008 13 2717-2728 Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . chebuloside II ÏàËÆ¶È:72.2% Natural Product Research 2001 15 35-42 Vanillic Acid 4-O-¦Â-D-(6'-O-Galloyl) Glucopyranoside and Other Constituents from the Bark of Terminalia macroptera Guill. Et Perr J¨¹rgen Conrad; Bernhard Vogler; Iris Klaiber; Sabine Reeb; Jan-Hinrich Guse; Gudrun Roos; Wolfgang Kraus Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2¦Á,3¦Â,23-trihydroxyolean-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:72.2% Acta Pharmaceutica Sinica 2006 Vol 41 835-839 A new triterpenoid saponin from stems of Akebia trifoliata GAO Hui-min; WANG Zhi-min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Alpinoside C30H46O4 ÏàËÆ¶È:72.2% Phytochemistry 1993 32 155-159 Triterpenoids from Sanguisorba alpina Zhong-Jian Jia, Xiang-Qian Liu, Zi-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . ilexoside XXXIV C36H57O13SNa ÏàËÆ¶È:72.2% Phytochemistry 1993 33 1475-1480 Triterpenes and triterpene glycosides from the leaves of Ilex rotunda Kayoko Amimoto, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxyolea-12-en-28-oic acid ¦Â-D-glu-copyranosyl ester C36H58O11 ÏàËÆ¶È:72.2% Journal of Natural Medicines 2009 63 318-322 A new diterpenoid and a new triterpenoid glucosyl ester from the leaves of Callicarpa japonica Thunb. var. luxurians Rehd. Masateru Ono, Tomoyo Chikuba, Kenji Mishima, Toru Yamasaki and Tsuyoshi Ikeda, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 28-O-¦Â-D-glucopyranosyl oleanolic acid C26H58O8 ÏàËÆ¶È:72.2% Chinese Journal of Natural Medicines 2003 1 134-136 Triterpene and Saponins from Kochia scoparia WANG Hao; FAN Chun-Lin; WANG Bei; DAI Yue; YE Wen-Cai; ZHAO Shou-Xun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 2¦Á,3¦Â,23-trihydroxyurs-12-en-28-oic acid ¦Â-D-glucopyranosyl ester ÏàËÆ¶È:72.2% Chinese Journal of Natural Medicines 2009 7 206-209 Triterpene Saponins from the Leaves of Ilex pernyi XIE Guang-Bo; JIANG Yong; LEI Lian-Di; TU Peng-Fei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 2¦Á,3¦Á,19¦Á,24-tetrahydroxylurs-12-en-28-oic acid-28-¦Â-D-glucopranoside ÏàËÆ¶È:72.2% Chinese Journal of Natural Medicines 2009 7 421-424 Triterpenes from Prunella vulgaris QI Jin; HU Zheng-Fang; LIU Zhi-Jun; YU Bo-Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 2¦Á,3¦Â,19¦Á,24-tetrahydroxylurs-12-en-28-oic acid-28-¦Â-D-glucopranoside ÏàËÆ¶È:72.2% Chinese Journal of Natural Medicines 2009 7 421-424 Triterpenes from Prunella vulgaris QI Jin; HU Zheng-Fang; LIU Zhi-Jun; YU Bo-Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 2¦Á,3¦Â,7¦Á,23-tetrahydroxy-olean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside ÏàËÆ¶È:72.2% Archives of Pharmacal Research 1997 20 291-296 Constituents of the herb of Isodon excisus var. coreanus Ho Kyoung Kim, Wan Kyunn Whang and Il Hyuk Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . »ýÑ©²Ýµ¥ÌÇÜÕ ÏàËÆ¶È:72.2% Modern Chinese Medicine 2008 10(3) 7-9 Chemical studies on the saponin compounds of Centella asiatica Liu Yu, Zhao Yuqing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . rotungenoside C36H58O10 ÏàËÆ¶È:72.2% Bulletin of the Chemical Society of Japan 1989 62 469-473 The Structure of Rotungenoside, a New Bitter Triterpene Glucoside from Ilex Rotunda Munehiro Nakatani, Shuichi Hatanaka, Hajime Komura, Takashi Kubota, Tsunao Hase Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . ilexoside A ÏàËÆ¶È:70.7% Archives of Pharmacal Research 1987 10 132-141 New triterpenoid saponins fromIlex pubescens Yong Nam Han, Seung Kyung Bail, Tae Hee Kim and Byung Hoon Han Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 2¦Á,3¦Á,19,24-ËÄôÇ»ù-12-Ï©-ÎÚËÕËá-28-O-¦Â-D-ÆÏÌÑÌÇõ¥ ÏàËÆ¶È:70.2% Chinese Pharmaceutical Journal 2004 39 17-19 Study on the chemical constituents of Callicarpa bodinieri REN Feng zhi, HE Bing kun, LUAN Xin hui, ZHAO Yi min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . rubuside B C36H56O9 ÏàËÆ¶È:69.4% Journal of Natural Products 2009 72 1755-1760 Triterpenoid Saponins from Rubus ellipticus var. obcordatus Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . rubuside G C36H56O9 ÏàËÆ¶È:69.4% Journal of Natural Products 2009 72 1755-1760 Triterpenoid Saponins from Rubus ellipticus var. obcordatus Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . niga-ichigoside F1 ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 2003 51(2) 200-202 A New Triterpene Glucosyl Ester from the Fruit of the Blackberry (Rubus allegheniensis) Masateru ONO,Michiko TATEISHI, Chikako MASUOKA,Hiromasa KOBAYASHI,Keiji IGOSHI,Haruki KOMATSU,Yasuyuki ITO,Masafumi OKAWA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . quadranoside VIII C36H56O10 ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 2000 48(8) 1114-1120 Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . quadranoside X C36H58O11 ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 2000 48(8) 1114-1120 Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . 2¦Á,3¦Â,23-trihydroxyurs012,19-dien-28-oic acid 28-O-¦Â-D-glucopyranside ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 2000 48(8) 1114-1120 Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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