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²éѯ½á¹û£º¹²²éµ½5408¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Yemuoside YM20 C48H78O18 ÏàËÆ¶È:91.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Yemuoside YM18 C47H76O19 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Yemuoside YM17 C47H76O19 ÏàËÆ¶È:87.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Acanjaposide D C48H76O20 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . cussonside B C48H78O17 ÏàËÆ¶È:87.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Spinoside D3 C48H76O20 ÏàËÆ¶È:87.5% Phytochemistry 1993 33 891-895 3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . spinoside D3 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Oleanolic acid 28-O-[¦Á-Lrhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside C48H78O17 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . yiyeliangwanoside XI ÏàËÆ¶È:86.7% Phytochemistry 1995 38 695-698 Triterpenoid saponins from the bark of Nothopanax davidii Shi Shan Yu, De Quan Yu, Xiao Tian Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . nipponoside D ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . nipponoside D C48H78O19 ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . tauroside J ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . tauroside I ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Durantanin IV C48H78O20S ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . oleanolic acid 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glccopyranosyl(1¡ú6)-¦Â-D-glccopyranosyl ÏàËÆ¶È:85.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Spinoside D1 C48H76O19 ÏàËÆ¶È:85.4% Phytochemistry 1993 33 891-895 3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Spinoside D2 C48H74O20 ÏàËÆ¶È:85.4% Phytochemistry 1993 33 891-895 3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . spinoside D1 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . spinoside D2 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . liangwanoside II C53H84O23 ÏàËÆ¶È:84.9% Chemical & Pharmaceutical Bulletin 1987 35 1486-1490 Saponins from Chinese Folk Medicine, ¡°Liang Wang Cha, ¡± Leaves and Stems of Nothopanax delavayi, Araliaceae RYOJI KASAI,TOSHIHIKO OINAKA,CHONG-REN YANG,JUN ZHOU and OSAMU TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . liangwanoside II ÏàËÆ¶È:84.9% Journal of Chinese Pharmaceutical Sciences 1995 4 167-176 Triterpenoid Saponins from the Bark of Nothopanaxdavidii Shi-Shan; Yu; De-Quan Yu; Xiao-Tian Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . Acanjaposide E C48H76O20 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . Acanjaposide I C48H74O20 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . spinoside C1 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . spinoside C2 C48H76O19 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . spinoside C4 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . Spinoside C1 C48H78O18 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . Spinoside C5 C48H78O19 ÏàËÆ¶È:83.3% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . Glycoside C(3-epi-hederagenin) C48H78O18 ÏàËÆ¶È:83.3% Chemical Research in Chinese Universities 1994 10 185-192 Studies on the Glycosides in the Leaves of Oplopanax elatus NAKAI(I) WANG Guang-shu,ZHAO Chun-fang and XU Jing-da Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . akemisaponin J C47H74O18 ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 2012 60 1264-1274 Triterpene Saponins from the Pericarps of Akebia trifoliata Syuji Iwanaga, Tsutomu Warashina, Toshio Miyase Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 31 . Compound 2a ÏàËÆ¶È:81.6% Journal of Natural Medicines 2006 60 49-53 Triterpenoid saponins from cultural plants of Stenocereus stellatus (Cactaceae) Takeo Imai, Sachie Okazaki, Kaoru Kinoshita, Kiyotaka Koyama and Kunio Takahashi, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 32 . Yemuoside YM19 C47H74O18 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 33 . Acanjaposide F C48H76O20 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 34 . Acanjaposide H C48H76O19 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 35 . acanjaposide A C47H72O19 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 36 . nipponoside A C48H76O18 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 37 . cynarasaponin J methyl ester C48H76O19 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 1988 36 2466-2474 Sesquiterpene Glycosides and Saponins from Cynara cardunculus L. SHIGERU SHIMIZU,NAOMI ISHIHARA,KAORU UMEHARA,TOSHIO MIYASE and AKIRA UENO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 38 . spinoside C5 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 39 . compound 7 ÏàËÆ¶È:81.2% Acta Pharmaceutica Sinica 2004 Vol 39 354-358 Structures of four new triterpenoid saponins from the leaves of Oplopanax elatus Nakai WANG Guang-shu; YANG Xiao-hong; XU Jing-da Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 40 . 3-O-¦Á-L-RhamnopyranosyL(1¡ú3)-¦Â-D-glucopyranosyl-28-O-¦Â-D-glucopyranosyl oleanolic acid ÏàËÆ¶È:81.2% Phytochemistry 1995 40 1765-1767 Triterpenoidal saponins from Dumasia Truncata Junei Kinjo, Kumi Suyama, Toshihiro Nohara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 41 . Spinoside C4 C48H76O19 ÏàËÆ¶È:81.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 42 . oleunolic acid 3-0-(3'-0-¦Á-L-rhamnopyranosyl)-¦Â-D-glucuronopyranoside-28-O-¦Â-D-glucopyranoside ÏàËÆ¶È:81.2% Phytochemistry 1984 23 2907-2910 Two saponins from Zexmenia buphthalmiflora Claudio D. Schteingart, Alicia B. Pomilio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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