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huadong1227木虫 (小有名气)
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[求助]
16 微谱数据求助 已有1人参与
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吡啶溶解， 16.53，16.58，16.74，17.42，17.74，18.69，18.92，19.14，19.67， 21.31，21.38，28.44，28.62，30.44，31.07，31.91，32.45，32.58， 32.74，34.48，34.54，37.39，37.40，37.45，37.77，39.25，40.00， 40.20，40.75，40.95，41.06，47.57，50.59，50.63，56.84，61.49， 63.07，63.14，64.19，64.44，68.59，69.82，70.67，71.95，72.00， 72.76，72.88，73.11，73.16，73.53，74.24，74.37，75.44，75.54， 77.26，77.98，78.02，78.25，78.36，78.72，78.76，78.84，78.87， 80.65，81.37，81.58，100.62，102.44，102.48，103.55，105.18，105.23， 110.95，112.94，122.09，141.10 |
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huadong1227: 金币+10, ★有帮助 2015-03-23 23:04:31
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huadong1227: 金币+10, ★有帮助 2015-03-23 23:04:31
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1 . clematomandshurica saponin C C76H124O39 相似度:72.3% Journal of Natural Products 2006 69 1591-1595 Triterpene Saponins from Clematis mandshurica Shepo Shi, Dan Jiang, Caixia Dong, and Pengfei Tu Structure 13C NMR 碳谱模拟图 2 . (25R)-3β-[(O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→2)-O-[O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)oxy]-22ξ-methoxy-5α-furostan-26-yl β-D-glucopyranoside C70H118O38 相似度:72% Chemical & Pharmaceutical Bulletin 2001 49(6) 726-731 Steroidal Glycosides from the Bulbs of Camassia leichtlinii and Their Cytotoxic Activities Minpei KURODA,Yoshihiro MIMAKI, Fusako HASEGAWA,Akihito YOKOSUKA, Yutaka SASHIDA,and Hiroshi SAKAGAMI Structure 13C NMR 碳谱模拟图 3 . 23-hydroxy-3β-[(O-α-L-rhamnopyranosyl-(1→2)-O-[O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid 28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester C71H116O36 相似度:72% Journal of Natural Products 2001 64 1226-1229 New Bisdesmosidic Triterpene Saponins from the Roots of Pulsatilla chinensis Yoshihiro Mimaki,Akihito Yokosuka, Minpei Kuroda, Mari Hamanaka, Chiseko Sakuma, and Yutaka Sashida Structure 13C NMR 碳谱模拟图 4 . tomentoside C70H114O34 相似度:72% Chinese Chemical Letters 1999 10 1035-1036 A New Triterpenoid Saponin from Anemone tomentosa Xun LIAO,Shu Lin PENG,Bo Gang LI,Yao Zu CHEN,Li Sheng DING Structure 13C NMR 碳谱模拟图 5 . 3-O-{[(α-L-rhamnospyranosyl(1→2)-(α-L-rhamnopyranosyl(1→2)-β-D-galactopyranosyl-(1→3)]-[β-D-glucopyranosyl(1→2)]-β-D-glucuronopyranosyl}barringtogenolC21,22-O-diangeloate C70H110O31 相似度:72% Phytochemistry 1997 44 491-495 A triterpenoid saponin from Maesa ramentacea Pittaya Tuntiwachwuttikul, Orasa Pancharoen, Wilawan Mahabusarakam, Pichaet Wiriyachitra, Walter C. Taylor, William A. Bubb, G. H. N. Towers Structure 13C NMR 碳谱模拟图 6 . (25R)-26-[(β-D-glucopyranosyl)oxy]-6α-hydroxy-22α-methoxy-5α-furostan-3β-yl O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranosyl-(1→2)-O-[O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside C70H118O39 相似度:72% Chemical & Pharmaceutical Bulletin 2009 57 1161-1166 Steroidal Glycosides from Furcraea foetida and Their Cytotoxic Activity Akihito Yokosuka, Tomoe Sano, Ken Hashimoto, Hiroshi Sakagami and Yoshihiro Mimaki Structure 13C NMR 碳谱模拟图 7 . Clematomandshurica saponin F C77H126O39 相似度:71.4% Planta Medica 2013 79 987-994 Triterpene Saponins from Clematis mandshurica and Their Antiproliferative Activity Gong, Yi-xia; Hua, Hui-ming; Xu, Yong-nan; Liu, Jian-yu; Yu, Zong-gui; Ma, Jing; Zhang, Hui; Jing, Yong-kui: Structure 13C NMR 碳谱模拟图 8 . Clematomandshurica saponin H C76H124O39 相似度:71.0% Planta Medica 2013 79 987-994 Triterpene Saponins from Clematis mandshurica and Their Antiproliferative Activity Gong, Yi-xia; Hua, Hui-ming; Xu, Yong-nan; Liu, Jian-yu; Yu, Zong-gui; Ma, Jing; Zhang, Hui; Jing, Yong-kui: Structure 13C NMR 碳谱模拟图 9 . furcreafurostatin methyl ether C70H118O38 相似度:70.6% Fitoterapia 2004 75 634-638 Saponins from Furcraea selloa var. marginata Joanne L. Simmons-Boyce, Winston F. Tinto,Stewart McLeanb, William F. Reynolds Structure 13C NMR 碳谱模拟图 10 . 3β-[(O-β-D-ribopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]olean-12-en-28-oic acid O-β-D-glucopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester C76H124O39 相似度:69.7% Chemical & Pharmaceutical Bulletin 2009 57 1425-1430 Triterpene Glycosides from the Whole Plant of Anemone hupehensis var. japonica and Their Cytotoxic Activity Akihito Yokosuka, Tomoe Sano, Ken Hashimoto, Hiroshi Sakagami and Yoshihiro Mimaki Structure 13C NMR 碳谱模拟图 11 . acacic acid 相似度:69.7% Bulletin of the Chemical Society of Japan 1995 68 3483-3490 Three New Triterpenoidal Saponins Acylated with Monoterpenic Acid from Albizziae Cortex Tsuyoshi Ikeda, Satoko Fujiwara, Junei Kinjo, Toshihiro Nohara, Yoshiteru Ida, Junzo Shoji, Tetsuro Shingu, Ryuichi Isobe, Tetsuya Kajimoto Structure 13C NMR 碳谱模拟图 12 . borivilianoside E C73H120O39 相似度:69.3% Journal of Natural Products 2009 72 177-181 Cytotoxic Spirostane-Type Saponins from the Roots of Chlorophytum boriWilianum Debabrata Acharya,Anne-Claire Mitaine-Offer, Nutan Kaushik, Tomofumi Miyamoto, Thomas Paululat,Jean-Franc¸ois Mirjolet, Olivier Duchamp, and Marie-Aleth Lacaille-Dubois Structure 13C NMR 碳谱模拟图 13 . compound 9 相似度:69.3% Chemistry of Natural Compounds 2006 42 49-54 TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.VI. GLYCOSIDES FROM LEAVES OF Kalopanax septemlobum VAR. typicum INTRODUCED TO CRIMEA D. A. Panov, V. I. Grishkovets, V. V. Kachala, and A. S. Shashkov Structure 13C NMR 碳谱模拟图 14 . compound 14 相似度:69.3% Chemistry of Natural Compounds 2006 42 49-54 TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.VI. GLYCOSIDES FROM LEAVES OF Kalopanax septemlobum VAR. typicum INTRODUCED TO CRIMEA D. A. Panov, V. I. Grishkovets, V. V. Kachala, and A. S. Shashkov Structure 13C NMR 碳谱模拟图 15 . tomentoside B C70H114O35 相似度:69.3% Journal of Natural Medicines 2012 66 Triterpenoid saponins from the root of Anemone tomentosa Yi Wang • Wei Kang • Liang-jian Hong •Wen-li Hai • Xiao-yang Wang • Hai-feng Tang •Xiang-rong Tian Structure 13C NMR 碳谱模拟图 16 . tomentoside B C70H114O35 相似度:69.3% Journal of Natural Medicines 2013 67 70-77 Triterpenoid saponins from the root of Anemone tomentosa Yi Wang, Wei Kang, Liang-jian Hong, Wen-li Hai… Structure 13C NMR 碳谱模拟图 17 . Clematiunicinoside D C70H114O34 相似度:69.3% Chemical & Pharmaceutical Bulletin 2014 62 35-44 Triterpenoid Saponins from the Roots of Clematis uncinata Shuo-Guo Li, Xiao-Jun Huang, Man-Mei Li, Mei Wang, Rui-Bing Feng, Wei Zhang, Yao-Lan Li, Ying Wang, Wen-Cai Ye Structure 13C NMR 碳谱模拟图 18 . Oleanolic acid 3-O-β-D-glucopyranosyl(1→3)-α-L-rhamnopyranosyl(1→2)[α-L-rhamnopyranosyl(1→6)-β-D-glucopyranosyl(1→4)]-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranosyl ester 相似度:68.8% Molecules 2012 17 5520-5531 Saponins with Neuroprotective Effects from the Roots of Pulsatilla cernua Jian-Yu Liu, Ying-Li Guan, Li-Bo Zou, Yi-Xia Gong, Hui-Ming Hua, Yong-Nan Xu, Hui Zhang, Zong-Gui Yu and Wen-Hao Fan Structure 13C NMR 碳谱模拟图 19 . compound A 相似度:68.4% Journal of Peking University (Health Sciences) 2004 36 421-425 Isolation and identification of chemical constituents from Albizia julibrissin Durazz ZHENG Lu; WU Gang; WANG Bin; WU Li jun; ZHAO Yu ying Structure 13C NMR 碳谱模拟图 |
2楼2015-03-23 21:13:32
