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tauroside J ÏàËÆ¶È:95.8% Chemistry of Natural Compounds 1992 28 593-596 TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cussonside B C48H78O17 ÏàËÆ¶È:91.6% China Journal of Chinese Materia Medica 2001 26 612-614 Studies on the Chemical Constituents from Anemone anhuiensis Y. K. Yang n. Wang et W. C. Ye ZHANG Qingwen, YE Wencai, CHE Chuntao, ZHAPO Shouxun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Oleanolic acid 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside C48H78O17 ÏàËÆ¶È:91.6% Natural Product Communications 2006 1 27-32 Clarification of the Saponin Composition ofRanunculus ficaria Tubers Andrew Marston, Martine Cabo, Christian Lubrano, Jean-Renaud Robin,Claude Fromageot and Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Yemuoside YM20 C48H78O18 ÏàËÆ¶È:89.5% Helvetica Chimica Acta 2008 Vol. 91 451 Unusual Nortriterpenoid Saponins from Stauntonia chinensis Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . tauroside I ÏàËÆ¶È:89.5% Chemistry of Natural Compounds 1992 28 593-596 TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Durantanin IV C48H78O20S ÏàËÆ¶È:89.5% Molecules 2009 14 1952-1965 New Triterpene Saponins from Duranta repens Linn. and Their Cytotoxic Activity Wafaa S. Ahmed, Mona A. Mohamed, Rabab A. El-Dib and Manal M. Hamed Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . oleanolic acid 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glccopyranosyl(1¡ú6)-¦Â-D-glccopyranosyl ÏàËÆ¶È:89.5% China Journal of Chinese Materia Medica 2008 33 1696-1699 Studies on chemical constituents from rhizome of Anemone flaccida ZHANG Lantian, TAKAISHI Yoshihisa, ZHANG Yanwen, DUAN Hongquan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ciwujianoside C3 ÏàËÆ¶È:89.5% West China Journal of Pharmaceutical Sciences 1990 5 132-135 Studies on saponins isolated from Schettlera Delavayi Harms ex diels Jian qenpen, Xian Zhuoyin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Yemuoside YM17 C47H76O19 ÏàËÆ¶È:89.3% Helvetica Chimica Acta 2008 Vol. 91 451 Unusual Nortriterpenoid Saponins from Stauntonia chinensis Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Gordonoside K C47H74O19 ÏàËÆ¶È:89.3% Journal of Natural Products 2011 74 1066-1072 Potential Anti-inflammatory Constituents of the Stems of Gordonia chrysandra Hui-Zheng Fu, Chuang-Jun Li, Jing-Zhi Yang, Zhu-Fang Shen, and Dong-Ming Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Acanjaposide H C48H76O19 ÏàËÆ¶È:87.5% Chemical & Pharmaceutical Bulletin 2005 53(9) 1147-1151 New Oleanene Glycosides from the Leaves of Acanthopanax japonicus Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . nipponoside D ÏàËÆ¶È:87.5% Phytochemistry 2002 59 379-384 nor-Oleanene type triterpene glycosides from the leaves of Acanthopanax japonicus Sang-Yong Park, Seung-Yeup Chang, O-Jin Oh,Chang-Soo Yook, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . kalopanax saponin G ÏàËÆ¶È:87.5% Journal of Natural Products 1999 62 445-448 Triterpenoid Saponins of Acanthopanax nipponicus Leaves Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . nipponoside D C48H78O19 ÏàËÆ¶È:87.5% Journal of Natural Products 1999 62 445-448 Triterpenoid Saponins of Acanthopanax nipponicus Leaves Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . kalopanaxsaponin G C48H78O18 ÏàËÆ¶È:87.5% Chemical & Pharmaceutical Bulletin 1991 39 865-870 Studies on the Constituents of the Bark of Kalopanax pictus NAKAI Kazuko SANO,Shuichi SANADA,Yoshiteru IDA and Junzo SHOJI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . HN-saponin H ÏàËÆ¶È:87.5% Chemical & Pharmaceutical Bulletin 1985 33 3324-3329 Studies on Nepalese Crude Drugs. III. On the Saponins of Hedera nepalensis K. KOCH. HARUHISA KIZU,SHINGO KITAYAMA,FUKIO NAKATANI,TSUYOSHI TOMIMORI and TSUNEO NAMBA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . glycoside pair f2 ÏàËÆ¶È:87.5% Chemistry of Natural Compounds 2006 42 61-66 TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.VII. MINOR GLYCOSIDES FROM STEMS OF Kalopanax septemlobumVAR. maximowiczii AND Kalopanax septemlobum VAR. typicum D. A. Panov, V. I. Grishkovets, V. V. Kachala, and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . spinoside C1 ÏàËÆ¶È:87.5% Phytochemistry 1997 46 1255-1259 3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 3b ÏàËÆ¶È:87.5% Acta Pharmaceutica Sinica 2000 Vol 35 821-825 NEW TRITERPENOID SAPONINS FROM ANEMONE BEGONIIFOLIA LIAO Xun; LI Bo gong; DING Li sheng; PAN Yuan jiang; CHEN Yao zu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Spinoside C1 C48H78O18 ÏàËÆ¶È:87.5% Phytochemistry 1993 34 1599-1602 3¦Á-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . tragopogonoside C methyl ester C48H76O19 ÏàËÆ¶È:87.5% Phytochemistry 1992 31 2087-2091 Tragopogonosides A-I, oleanane saponins from Tragopogon pratensis Toshio Miyase, Hiromi Kohsaka, Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . pulsatiloside C C48H78O18 ÏàËÆ¶È:87.5% Phytochemistry 1990 29 595-599 Triterpenoid saponins from Pulsatilla campanella Xing-Cong Li,De-Zu Wang,Su-Gong Wu,Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Hederagenin 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranoside C48H78O18 ÏàËÆ¶È:87.5% Chinese Pharmaceutical Journal 1996 31 522-524 GlycosidesintheleavesofOplopanaxelatus NakaiWangGuangshu(WangGS), MengQin(MengQ), XuJingda(XuJD), etal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . umbellatoside A C48H76O19 ÏàËÆ¶È:87.5% Helvetica Chimica Acta 2011 94 1850-1859 New Triterpenoid and Ergostane Glycosides from the Leaves of Hydrocotyle umbellata L. Adakarleny Sosa, Carmelo Rosquete, Luis Rojas, Laurent Pouys¨¦gu, St¨¦phane Quideau, Thomas Paululat, Anne-Claire Mitaine-Offer and Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . Hederagenin 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside C48H78O18 ÏàËÆ¶È:87.5% Natural Product Communications 2006 1 27-32 Clarification of the Saponin Composition ofRanunculus ficaria Tubers Andrew Marston, Martine Cabo, Christian Lubrano, Jean-Renaud Robin,Claude Fromageot and Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . scheffleroside II ÏàËÆ¶È:87.5% West China Journal of Pharmaceutical Sciences 1990 5 132-135 Studies on saponins isolated from Schettlera Delavayi Harms ex diels Jian qenpen, Xian Zhuoyin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . Yemuoside YM18 C47H76O19 ÏàËÆ¶È:87.2% Helvetica Chimica Acta 2008 Vol. 91 451 Unusual Nortriterpenoid Saponins from Stauntonia chinensis Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . aralia-saponin I C47H76O18 ÏàËÆ¶È:87.2% Chemical & Pharmaceutical Bulletin 2000 48(6) 838-842 Four New Saponins from the Root Bark of Aralia elata Shao-jiang SONG,Norio NAKAMURA,Chao-mei MA,Masao HATTORI and Sui-xu XU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . oleanolic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-xylopyranosyl (1¡ú6)]-¦Â-D-glucopyranosyl ester C47H76O16 ÏàËÆ¶È:87.2% Archives of Pharmacal Research 2007 30 1-7 Antioxidant constituents and a new triterpenoid glycoside fromFlos Lonicerae Chun-Whan Choi, Hyun Ah Jung, Sam Sik Kang and Jae Sue Choi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . rotundioside K C48H77O22S ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 2006 54(12) 1694-1704 Antiproliferative Constituents from Umbelliferae Plants. IX.New Triterpenoid Glycosides from the Fruits of Bupleurum rotundifolium Toshihiro FUJIOKA,Keisuke YOSHIDA, Hiroko SHIBAO, Tsuneatsu NAGAO, Miyako YOSHIDA,Kazuhisa MATSUNAGA, Jiro TAKATA, Yoshiharu KARUBE, Yukiko IWASE,Hikaru OKABE, and Kunihide MIHASHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . Acanjaposide D C48H76O20 ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 2005 53(9) 1147-1151 New Oleanene Glycosides from the Leaves of Acanthopanax japonicus Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . Acanjaposide F C48H76O20 ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 2005 53(9) 1147-1151 New Oleanene Glycosides from the Leaves of Acanthopanax japonicus Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . eclalbasaponin IV C42H68O14 ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 1994 42 1336-1338 Oleanane Glycosides from Eclipta alba Shoji YAHARA,Ning DING and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . cirensenoside O C48H78O17 ÏàËÆ¶È:85.4% Acta Pharmaceutica Sinica 1996 31 940-944 ISOLATION AND STRUCTURE ELUCIDATION OF CIRENSENOSIDES O AND P FROM THE LEAVES OF OPLOPANAX ELATUS NAKAL GS Wang; YP Chen; JD Xu; T Murayama and J Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . spinoside C4 ÏàËÆ¶È:85.4% Phytochemistry 1997 46 1255-1259 3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . spinoside C5 ÏàËÆ¶È:85.4% Phytochemistry 1997 46 1255-1259 3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . hederagenin 28-O-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-glucopyranosyl (1¡ú6)-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:85.4% Acta Pharmaceutica Sinica 2007 Vol 42 862-866 Triterpene glycosides from the aerial parts of Pulsatilla chinensis SHI Bao-jun; Li Qian; ZHANG Xiao-qi; WANG Ying; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . kizuta saponin K3 ÏàËÆ¶È:85.4% Phytochemistry 1995 38 1473-1479 Triterpenoid saponins from Clematis chinensis Baoping Shao, Guowei Qin, Rensheng Xu, Houming Wu, Kan Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . PS-3 ÏàËÆ¶È:85.4% Phytochemistry 1993 33 83-86 Molluscicidal and antifungal triterpenoid saponins from Rapanea melanophloeos leaves Kazuhiro Ohtani, Steven Mavi, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . hederagenin 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl (1¡ú6)-¦Â-D-glucopyranosyl] ester ÏàËÆ¶È:85.4% Phytochemistry 1993 33 1469-1473 Triterpenoid glycosides from Stauntonia hexaphylla Huai-Bin Wang, Ralf Mayer, Gerhard R¨¹cker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . Spinoside C5 C48H78O19 ÏàËÆ¶È:85.4% Phytochemistry 1993 34 1599-1602 3¦Á-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . tragopogonoside D methyl ester C48H76O19 ÏàËÆ¶È:85.4% Phytochemistry 1992 31 2087-2091 Tragopogonosides A-I, oleanane saponins from Tragopogon pratensis Toshio Miyase, Hiromi Kohsaka, Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . heragenin 28-O-¦Á-L-rhamnopyranosyl(¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl ester] ÏàËÆ¶È:85.4% Chinese Traditional and Herbal Drugs 2008 39 819-822 Ð˰²°×Í·Î̸ù¾¥µÄ»¯Ñ§³É·ÖÑо¿ Ëï»Ô;ÀîÜç;Ò¶ÎIJÅ;ÕÔÊØÑµ;Ò¦ÐÂÉú Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . congmuyenoside I C48H78O19 ÏàËÆ¶È:85.4% Food Chemistry 2013 138 208-213 Studies on cytotoxic triterpene saponins from the leaves of Aralia elata Yan Zhang, Ying Peng, Lingzhi Li, Lei Zhao, Yan Hu, Chong Hu, Shaojiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . ecliptasaponin B C48H78O19 ÏàËÆ¶È:85.4% Food Chemistry 2013 138 208-213 Studies on cytotoxic triterpene saponins from the leaves of Aralia elata Yan Zhang, Ying Peng, Lingzhi Li, Lei Zhao, Yan Hu, Chong Hu, Shaojiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . centellasaponin D C48H78O19 ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 2011 49 1368-1371 Medicinal Foodstuffs. XXVII.1) Saponin Constituents of Gotu Kola (2):Structures of New Ursane- and Oleanane-Type Triterpene Oligoglycosides,Centellasaponins B, C, and D, from Centella asiaticaCultivated in Sri Lanka Hisashi MATSUDA, Toshio MORIKAWA, Hiroki UEDA, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . compound 5 C48H78O19 ÏàËÆ¶È:85.4% Natural Medicines 2001 55 134-138 Five New Triterpene Glycosides from Centella asiatica KURODA Minpei,MIMAKI Yoshihiro, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . compound 6 C48H78O19 ÏàËÆ¶È:85.4% Natural Medicines 2001 55 134-138 Five New Triterpene Glycosides from Centella asiatica KURODA Minpei,MIMAKI Yoshihiro, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . kalopanaxsaponin G ÏàËÆ¶È:85.4% Chinese Traditional and Herbal Drugs 2012 43 2141-2145 Study on glycosides from stems of Schefflera kwangsiensis ZHANG Qiao; SHEN Juan; ZHAO Yi-wu; WANG Zhen-zhong; XIAO Wei; Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . centellasaponin D C48H78O19 ÏàËÆ¶È:85.4% Chemical & Pharmaceutical Bulletin 2001 49 1368-1371 Medicinal Foodstuffs. XXVII. Saponin Constituents of Gotu Kola (2): Structures of New Ursane- and Oleanane-Type Triterpene Oligoglycosides, Centellasaponins B, C, and D, from Centella asiatica Cultivated in Sri Lanka Hisashi MATSUDA, Toshio MORIKAWA, Hiroki UEDA, Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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