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Ò©Íè¶ù1987: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-11 15:00:25
Ò©Íè¶ù1987(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-09-21 11:29:22
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²éѯ½á¹û£º¹²²éµ½1016¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-(¦Á-L-rhamnopyranosyl(1-4))-¦Â-D-glucopyranoside ÏàËÆ¶È:79.4% Chinese Chemical Letters 1993 4 137-138 TWO MINOR SPIROSTANOL GLYCOSIDES FROM YONG JU,ZHONG JIAN JIA,HAI RUO PENG AND XUE JUN SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Á-1-rhamnopyranosyl(1¡ú4)]-¦Â-D-galactopyranoside ÏàËÆ¶È:79.4% Phytochemistry 1994 37 1433-1436 Steroidal saponins from Smilax menispermoidea and S. Lebrunii Ju Yong, Jia Zhongjian, Sun Xuejun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . pennogenin-3-O-¦Á-L-arabinofuranosyl-(1¡ú4)-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glcopyranoside C44H72O17 ÏàËÆ¶È:77.2% Chemical & Pharmaceutical Bulletin 1982 30 712-718 Steroid Saponins from Paris polyphylla SM.-Supplement MITSUHIKO MIYAMURA,KIMIKO NAKANO,TOSHIHIRO NOHARA,TOSHIAKI TOMIMATSU and TOSHIO KAWASAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranoside ÏàËÆ¶È:76.9% Chemistry of Natural Compounds 2007 43 672-677 SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 13 C39H62O13 ÏàËÆ¶È:76.9% Steroids 2013 78 670-682 Steroidal glycosides from the bulbs of Fritillaria meleagris and their cytotoxic activities Yukiko Matsuo, Daisuke Shinoda, Aina Nakamaru, Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Paris Saponins VII ÏàËÆ¶È:76.9% Natural Product Research and Development 2011 23 1017-1020 Chemical Constituents of Phyllanthus niruri L. ZHU, Hong-lin, WEI, Wan-xing, ZHOU, Min, YANG, Dan, FAN, Xi-wang, LIU, Jian-xiong Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-[¦Á-L-arabinofuranosyl(1¡ú4)]-¦Â-D-glucopyranoside ÏàËÆ¶È:74.3% Chemistry of Natural Compounds 2007 43 672-677 SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 7 ÏàËÆ¶È:74.3% Phytochemistry 1994 36 1005-1008 Steroidal prosapogenins from Dioscorea olfersiana Mitsue Haraguchi, Ana Paula Zaccarias Dos Santos, Maria Claudia Marx Young, Edison Paulo Chui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . pallidifloside C C39H62O14 ÏàËÆ¶È:74.3% Journal of Asian Natural Products Research 2011 13 1014-1022 Three new steroidal saponins from Fritillaria pallidiflora Shuo Shen, Chao-Jun Chen, Ren Bu, Lu Ga, Guo-Yu Li, Yong Tan, Xian Li and Jin-Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . pennogenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl-(1¡ú4)-¦Â-D-glucopyranoside C44H70O17 ÏàËÆ¶È:72.7% Chinese Chemical Letters 2008 19 82-84 A new C27-steroidal glycoside from Ophiopogon japonicus Jian Zhong Wang , Li Ming Ye, Xiao Bing Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Paris Saponins H ÏàËÆ¶È:72.7% Natural Product Research and Development 2011 23 1017-1020 Chemical Constituents of Phyllanthus niruri L. ZHU, Hong-lin, WEI, Wan-xing, ZHOU, Min, YANG, Dan, FAN, Xi-wang, LIU, Jian-xiong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compopund 15 ÏàËÆ¶È:71.7% Chemical & Pharmaceutical Bulletin 1982 30 712-718 Steroid Saponins from Paris polyphylla SM.-Supplement MITSUHIKO MIYAMURA,KIMIKO NAKANO,TOSHIHIRO NOHARA,TOSHIAKI TOMIMATSU and TOSHIO KAWASAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 25(R)-pennogenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranoside ÏàËÆ¶È:71.7% Chemistry of Natural Compounds 2008 44 821-823 STEROIDAL SAPONINS FROM Paris mairei Xiao-xiao Liu, Lei Wang,Jie Yang, and Qiang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Pennogenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú3)-¦Â-Dglucopyranoside ÏàËÆ¶È:71.7% Archives of Pharmacal Research 2008 31 653-658 In vivo anti-inflammatory effect of a new steroidal saponin, mannioside A, and its derivatives isolated from Dracaena mannii Leon Azefack Tapondjou, Kemvoufo Beaudelaire Ponou, Remy Bertrand Teponno, Marius Mbiantcha and Jules D¨¦sir¨¦ Djoukeng, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . pennogenin diglycoside C39H60O12 ÏàËÆ¶È:71.7% Chinese Journal of Medicinal Chemistry 2005 15 25-30 Isolation and identif iciation of steroidal saponins from Paris polyphylla Smith KANG Li-ping, MA Bai-ping, ZHANG Jie, XIONG Cheng-qi, TAN Da-wei, CONG Yu-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (25S)-nuatigenin-3-O-¦Á-L-rhanmopyransoyl-(1¡ú2)-¦Â-D-glucopyranoside ÏàËÆ¶È:71.7% Natural Product Research and Development 2007 19 956-959 Metabolites of Endophytic Fungus GT20036029 Isolated from the Mangrove Plant Hibiscus tiliaceus LI Li-ya;DENG Zhi-wei; YU Shan-jiang; GU Jia; LIN Wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Tb ÏàËÆ¶È:71.7% Chinese Jouranl of Magnetic Resonance 2012 29 101-111 An NMR Study on Two Glucosylated Steroidal Saponins of Tb KANG Li-ping, WANG Yong-ze, FENG Bing, ZHOU Wen-bin, XIONG Cheng-qi, ZHAO Yang, TAN Da-wei, LIU Chao, MA Bai-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (25S)-17¦Á,27-dihydroxyspirost-5-en-3¦Â-yl O-(4-O-acetyl-¦Á-L-rhamnopyranosyl)-(1¡ú2)-¦Â-D-glucopyranoside C41H64O15 ÏàËÆ¶È:70.7% Phytochemistry 2008 69 2724-2730 Steroidal glycosides from the underground parts of Trillium erectum and their cytotoxic activity Akihito Yokosuka , Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . pennogenin-3-O-¦Á-L-arabinofuranosyl(1¡ú4)-[¦Á-L-rhamnopy-ranosyl(1¡ú2)]-¦Â-D-glycopyranoside ÏàËÆ¶È:70.4% China Journal of Chinese Materia Medica 2009 34 1812-1815 Chemical constituents from herbs of Paris verticillata HUANG Xianxiao, GAO Wenyuan, MAN Shuli, YAN Juanjuan, WANG Yanli Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-¦Â-D-glucopyranosyl(1¡ú4)-[¦Á-1-rhamnopyranosyl(1¡ú6)]-¦Â-D-galactopyranoside ÏàËÆ¶È:70.4% Phytochemistry 1994 37 1433-1436 Steroidal saponins from Smilax menispermoidea and S. Lebrunii Ju Yong, Jia Zhongjian, Sun Xuejun Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . pennogenin-3-O-¦Á-L-arabinofuranosyl(1¡ú4)-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glycopyranoside ÏàËÆ¶È:70.4% China Journal of Chinese Materia Medica 2010 35 2994-2998 Flavone and steroid chemical constituents from rhizome of Paris axialis HUANG Xianxiao; GAO Wenyuan; ZHAO Wanshun; ZHANG Tiejun; XU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ƫŵÔíÜÕÔª-3-O-¦Á-L-߻૰¢À²®ÌÇ»ù(1¡ú 4)-[¦Á-L-ßÁà«ÊóÀîÌÇ»ù(1¡ú 2)]-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ C44H70O17 ÏàËÆ¶È:70.4% Chinese Traditional and Herbal Drugs 2009 40 1366-1369 Ã«ÖØÂ¥µÄ»¯Ñ§³É·ÖÑо¿ »ÆÏÍУ;¸ßÎÄÔ¶;¹È¿ËÈÊ;Âí³¬Ò» Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (3¦Â,17¦Á,25R)-spirost-5-ene-3,17-diol-3-O-¦Â-D-apiofuranosyl-(1¡ú3)-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside C44H70O17 ÏàËÆ¶È:70.4% Phytochemistry 2012 81 133-143 Steroidal saponins from Paris polyphylla var. yunnanensis Xia Wu, Lei Wang, Hui Wang, Yi Dai, Wen-Cai Ye, Yao-Lan Li Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ƫŵÔíÜÕÔª-3-O-¦Á-L-߻૰¢À²®ÌÇ»ù-(1¡ú4)-[¦Á-L-ßÁà«ÊóÀîÌÇ»ù-(1¡ú2)]-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ C44H70O17 ÏàËÆ¶È:70.4% Chinese Traditional and Herbal Drugs 2011 42 1917-1920 Chemical constituents in Paris polyphylla var. pseudothibetica ZHAO, Zhi-yong, GAO, Wen-yuan, HUANG, Xian-xiao, ZHAO, Wan-shun, ZHANG, Qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (25R,26R)-26-methoxyspirost-5-ene-3¦Â,17¦Á-diol 3-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside C40H64O14 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1998 46 1829-1832 New Steroidal Constituents from the Bulbs of Lilium candidum Yoshihiro MIMAKI,Tadashi SATOU,Minpei KURODA,Yutaka SASHIDA and Yoshio HAYAKEYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (25S)-27-hydroxypenogenin 3- O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside C39H62O14 ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 2007 55(4) 551-556 Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . trikamsteroside A C39H62O14 ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 2007 55(4) 551-556 Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-Dglucopyranoside ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 2007 55(4) 551-556 Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (25S)spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Â-D-glucopyranosy(1-4)[¦Á-L-arabinopyranpsy](1-6)]-¦Â-D-glucopyranoside ÏàËÆ¶È:69.2% Chinese Chemical Letters 1992 3 431-432 NEW MINOR STEROIDAL SAPONINS FROM SMILAXLEBRUNII ZHONG JIAN JIA,YONG JU AND MEI DU Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (25S)-spirost-5-en-3¦Â,17¦Á,27-triol-3-O-[¦Á-L-arabinopyranosyl(1¡ú6)]-¦Â-D-glucopyranoside ÏàËÆ¶È:69.2% Phytochemistry 1993 33 1193-1195 Minor steroidal glycosides from the roots of Smilax lebrunii Ju Zhong-Jian Jia Yong Structure 13C NMR ̼Æ×Ä£Äâͼ |
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