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破曉米修新蟲 (小有名氣)
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[求助]
維普數(shù)據(jù)求助！麻煩大家了！
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氘代試劑：氘代吡啶 16.3 ， 17.1， 18.1， 19.0 ，19.5 ，20.5， 26.6， 28.8， 29.3 ，30.6， 38.0 ，39.6， 39.9 ，40.5，41.4 ，42.7，42.9 ，47.6， 48.7 ，56.4， 61.9， 69.7， 70.9 ，71.4， 73.1， 73.2 ，74.0， 74.4， 74.5， 75.0 ，75.8， 77.1 ， 77.6 ，78.5 ， 78.8 ，79.1 ， 79.2 ，79.8， 80.1 ，80.3， 96.3， 96.5， 103.3 ，105.4， 123.7， 144.2， 177.0 |
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wangkaibo123
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kerry
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2樓2013-10-23 18:24:37
破曉米修
新蟲 (小有名氣)
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氘代試劑：氘代吡啶 16.3 , 17.1, 18.1,19.0 ,19.5 ,20.5, 26.6, 28.8, 29.3 ,30.6, 38.0 ,39.6,39.9 ,40.5,41.4 ,42.7,42.9 ,47.6, 48.7 ,56.4, 61.9,69.7, 70.9,71.4, 73.1, 73.2 ,74.0, 74.4, 74.5, 75.0,75.8, 77.1 , 77.6 ,78.5 ,78.8 ,79.1 , 79.2 ,79.8, 80.1 ,80.3, 96.3, 96.5, 103.3 ,105.4,123.7, 144.2, 177.0 |
3樓2013-10-23 22:23:03
wangkaibo123
榮譽版主 (職業(yè)作家)
kerry
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專家經(jīng)驗: +726 - PhEPI: 3
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破曉米修: 金幣+15, ★★★很有幫助 2013-10-24 14:49:23
破曉米修: 金幣+15, ★★★很有幫助 2013-10-24 14:49:23
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查詢模式：模糊查詢 碳譜數(shù)據(jù)輸入： 按從小到大順序輸入，數(shù)字間用英文半角逗號(,)分隔例如： 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 溶劑選項： 匹配容差： (數(shù)字格式，可自行設(shè)定) 相似度： %(相似度>=50%) 查詢結(jié)果：共查到4937個化合物(查詢結(jié)果僅供參考) 1 . Yemuoside YM17 C47H76O19 相似度:85.1% 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 碳譜模擬圖 2 . Yemuoside YM20 C48H78O18 相似度:83.3% 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 碳譜模擬圖 3 . spinoside C4 相似度:83.3% Phytochemistry 1997 46 1255-1259 3α-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 碳譜模擬圖 4 . Spinoside C5 C48H78O19 相似度:83.3% Phytochemistry 1993 34 1599-1602 3α-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR 碳譜模擬圖 5 . nipponoside D 相似度: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 碳譜模擬圖 6 . nipponoside D C48H78O19 相似度: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 碳譜模擬圖 7 . oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glccopyranosyl(1→6)-β-D-glccopyranosyl 相似度:81.2% 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 碳譜模擬圖 8 . cussonside B C48H78O17 相似度:81.2% 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 碳譜模擬圖 9 . Spinoside D3 C48H76O20 相似度:81.2% 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 碳譜模擬圖 10 . spinoside D3 相似度:81.2% Phytochemistry 1993 34 1599-1602 3α-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR 碳譜模擬圖 11 . Oleanolic acid 28-O-[α-Lrhamnopyranosyl(1→4)-β-D-glucopyranosyl-(1→6)] β-D-glucopyranoside C48H78O17 相似度:81.2% 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 碳譜模擬圖 12 . Yemuoside YM18 C47H76O19 相似度:80.8% 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 碳譜模擬圖 13 . Acanjaposide D C48H76O20 相似度:79.1% 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 碳譜模擬圖 14 . Acanjaposide I C48H74O20 相似度:79.1% 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 碳譜模擬圖 15 . tauroside J 相似度:79.1% 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 碳譜模擬圖 16 . tauroside I 相似度:79.1% 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 碳譜模擬圖 17 . Durantanin IV C48H78O20S 相似度:79.1% 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 碳譜模擬圖 18 . Glycoside C(3-epi-hederagenin) C48H78O18 相似度:79.1% 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 碳譜模擬圖 19 . Yemuoside YM19 C47H74O18 相似度:78.7% 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 碳譜模擬圖 20 . compound 7 相似度:78.7% 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 碳譜模擬圖 21 . 3-O-[α-L-rhamnopyranosyl-(1→2)-β-Dgalactopyranosyl-(1→2)-β-D-glucuronopyranosyl]-3β,16β,22α-trihydroxy-olean-12-ene C48H78O18 相似度:77.0% Journal of Natural Products 2007 70 979-983 Oleanane Saponins from Stylosanthes erecta Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca Structure 13C NMR 碳譜模擬圖 22 . spinoside C1 相似度:77.0% Phytochemistry 1997 46 1255-1259 3α-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 碳譜模擬圖 23 . Spinoside D1 C48H76O19 相似度:77.0% 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 碳譜模擬圖 24 . Spinoside D2 C48H74O20 相似度:77.0% 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 碳譜模擬圖 25 . Spinoside C1 C48H78O18 相似度:77.0% Phytochemistry 1993 34 1599-1602 3α-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji Structure 13C NMR 碳譜模擬圖 |
4樓2013-10-24 12:37:00
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