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lg1024½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
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12.42,12.59,15.74,16.95,17.14,18.24,18.32,23.53,23.68,23.96,25.75,27.97,28.23,30.75,33.28,36.74,39.19,39.39,39.60,39.81,40.02,40.23,40.44,40.65,41.07,41.27,41.86,46.73,55.47,66.23,68.31,69.81,69.96,70.12,70.97,71.16,71.70,71.74,74.14,74.38,76.53,77.21,79.37,101.39,104.85,105.11,105.64,111.78,111.83,122.11,126.89,127.07,143.38,143.72,144.01,146.15,166.48,166.75,175.92 DMSO |
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lg1024: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-27 14:52:35
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lg1024: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-27 14:52:35
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1 . scabiosaponin E C58H94O25 ÏàËÆ¶È:69.4% Journal of Natural Products 2004 67 604-613 New Biologically Active Triterpenoid Saponins from Scabiosa tschiliensis Quan Zheng, Kazuo Koike, Li-Kun Han, Hiromichi Okuda, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â-[(O-¦Â-D-glucopyranosyl-(1¡ú4)-O-¦Â-D-ribopyranosyl-(1¡ú3)-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl)oxy] olean-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester C58H94O25 ÏàËÆ¶È:69.4% Journal of Natural Products 2004 67 1511-1516 Triterpene Saponins from the Roots of Clematis chinensis Yoshihiro Mimaki, Akihito Yokosuka, Mari Hamanaka, Chiseko Sakuma, Takao Yamori, and Yutaka Sashida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . anemoside A ÏàËÆ¶È:69.4% Acta Botanica Sinica 1996 38 757-760 The Chemical Constituents of Anemon erivularis Peng Shu-lin, Ding Li-sheng, WangMing-kui and Chen Pei-qing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . begoniifolide A C59H96O26 ÏàËÆ¶È:69.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . huzhongoside B ÏàËÆ¶È:69.4% Phytochemistry 1996 42 821-825 Saponins from Clematis chinensis Baoping Shao, Guowei Qin, Rensheng Xu, Houming Wu, Kan Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-O-¦Â-D-ribopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl oleanolic acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside C58H94O25 ÏàËÆ¶È:69.4% Planta Medica 2014 80 942-948 Triterpenoid Saponins from the Roots of Clematis argentilucida and Their Cytotoxic Activity Zhao, Mei; Ma, Ning; Qiu, Feng; Hai, Wen-Li; Tang, Hai-Feng; Zhang, Yan; Wen, Ai-Dong: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . squarroside III ÏàËÆ¶È:67.7% Chemical & Pharmaceutical Bulletin 2000 48(6) 828-831 Four New Triterpene Glycosides from Thalictrum squarrosum Hitoshi YOSHIMITSU,Makiko NISHIDA,Zhong-Zhi QIAN,Zhen-Huan LEI and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . scabiosaponin D C59H96O26 ÏàËÆ¶È:67.7% Journal of Natural Products 2004 67 604-613 New Biologically Active Triterpenoid Saponins from Scabiosa tschiliensis Quan Zheng, Kazuo Koike, Li-Kun Han, Hiromichi Okuda, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . flaccidoside II C59H96O25 ÏàËÆ¶È:67.7% Planta Medica 1991 57 572-574 Two New Oleanane Saponins from Anemoneflaccida LiZhao, Wei-ming Chen, and Qi-cheng Fang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . flaccidoside III C59H96O26 ÏàËÆ¶È:67.7% Planta Medica 1991 57 572-574 Two New Oleanane Saponins from Anemoneflaccida LiZhao, Wei-ming Chen, and Qi-cheng Fang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-O-¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl oleanolic acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl ester C59H96O26 ÏàËÆ¶È:67.7% Chemistry of Natural Compounds 2009 45 514-518 TRITERPENE GLYCOSIDES FROM Lonicera.II. ISOLATION AND STRUCTURAL DETERMINATIONOF GLYCOSIDES FROM FLOWER BUDSOF Lonicera macranthoides Yu Chen, Xu Feng, Ming Wang, Xiaodong Jia, Youyi Zhao, and Yunfa Dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Glycosides K1 ÏàËÆ¶È:67.7% Chemistry of Natural Compounds 2000 36 295-298 TRITERPENE GLYCOSIDES OF Scheffleropsis angkae.II. STRUCTURE OF GLYCOSIDES L-El, L-E2, L-KI, AND L-K 2 A. S. Stolyarenko, I V. I. Grishkovets, A. S. Shashkov, and V. Ya Chirva t Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Glycoside F1 ÏàËÆ¶È:67.7% Chemistry of Natural Compounds 1999 35 547-551 TRITERPENE GLYCOSIDES FROM Tupidanthus calyptratus.I. STRUCTURE OF GLYCOSIDES B l, B2, F i, AND F 2 FROM LEAVES OF HOODED TUPIDANTHUS V. I. Grishkovets Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . flaccidoside II C59H96O25 ÏàËÆ¶È:67.7% 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 15 . mateglycoside A C59H96O26 ÏàËÆ¶È:67.7% Chemical & Pharmaceutical Bulletin 2009 57 257-261 Brazilian Natural Medicines. III. Structures of Triterpene Oligoglycosides and Lipase Inhibitors from Mate, Leaves of Ilex paraguariensis Sachiko Sugimoto, Seikou Nakamura, Sachiyo Yamamoto, Chihiro Yamashita, Yoshimi Oda, Hisashi Matsuda and Masayuki Yoshikawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Yemuoside YM12 ÏàËÆ¶È:67.7% Magnetic Resonance in Chemistry 2008 46 630-637 Five new bidesmoside triterpenoid saponins from Stauntonia chinensis (pages 630¨C637) Gao Hao, Wang Zhao, Yang Lei, Yu Yang, Yao Zhi-Hong, Wang Nai-Li, Zhou Guang-Xiong, Ye Wen-Cai and Yao Xin-Sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . hederasaponin B ÏàËÆ¶È:67.7% Natural Product Research and Development 1999 11(4) 1-6 CHEMICAL CONSTITUENTS FROM ANEMONE RUPESTRIS SSP. GELIDA Liao Xun; Chen Yaozu; Ding Lisheng; Li Bogang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-¦Á-L-ßÁà«ÊóÀîÌÇ(1¡ú2)-¦Á-L-ßÁà«Ä¾ÌÇ-Æë¶Õ¹ûËá-28-O-¦Á-L-ßÁà«ÊóÀîÌÇ(1¡ú4)-¦Â-D-ßÁà«ÆÏÌÑÌÇ(1¡ú6)-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ C59H96O25 ÏàËÆ¶È:67.7% Journal of Chinese Medicinal Materials 2009 32 1059-1062 Studies on Triterpenoid Saponins in the Rhizome of Anemone flaccida HAN Lin-tao, HUANG Fang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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