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linkus1988木虫 (正式写手)
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[求助]
求助微谱数据查询
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溶剂:氘代甲醇 碳谱数据:20.1,21.8,23.3,25.0,25.6,28.9,30.3,37.9,38.8,39.7,40.7,42.9,62.7,65.7,69.2,71.7,73.2,75.2,78.0,78.2,102.3,103.9,125.1,125.4,138.4 相似度:>=50% |
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wangkaibo123
荣誉版主 (职业作家)
kerry
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专家经验: +726 - PhEPI: 3
- 应助: 1928 (讲师)
- 贵宾: 0.598
- 金币: 7869.1
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- 管辖: 药学
【答案】应助回帖
★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
PSA: 金币+2, 3u 2013-06-24 12:40:59
linkus1988: 金币+10, ★★★★★最佳答案, 多谢 2013-06-24 15:50:38
感谢参与,应助指数 +1
PSA: 金币+2, 3u 2013-06-24 12:40:59
linkus1988: 金币+10, ★★★★★最佳答案, 多谢 2013-06-24 15:50:38
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按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如: 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 20.1,21.8,23.3,25.0,25.6,28.9,30.3,37.9,38.8,39.7,40.7,42.9,62.7,65.7,69.2,71.7,73.2,75.2,78.0,78.2,102.3,103.9,125.1,125.4,138.4 溶剂选项: 全部 CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN 查询空值 匹配容差: (数字格式,可自行设定) 相似度: %(相似度>=50%) 查询结果:共查到176个化合物(查询结果仅供参考) -------------------------------------------------------------------------------- 1 . 3,9-dihydroxymegastigmast-5-ene-3-O-[β-D-glucopyranosyl-(1→6)]-β-D-glucopyranoside 相似度:76% Journal of Agricultural and Food Chemistry 2006 54 9592-9597 Spectroscopic Identification and Antioxidant Activity of Glucosylated Carotenoid Metabolites from Cydonia vulgaris Fruits Antonio Fiorentino, Brigida D'Abrosca, Severina Pacifico, Claudio Mastellone, Vincenzo Piscopo, and Pietro Monaco Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 2 . (3R,9S)-megastigman-5-en-3,9-diol 3-O-[α-L-arabinofuranosyl-(1→6)]-β-D-glucopyranoside C24H42O11 相似度:72% Chemical & Pharmaceutical Bulletin 2005 53(7) 783-787 A Monoterpene Glucoside and Three Megastigmane Glycosides from Juniperus communis var. depressa Tsutomu NAKANISHI,Naoki IIDA,Yuka INATOMI,Hiroko MURATA,Akira INADA,Jin MURATA,Frank A. LANG,Munekazu IINUMA,Toshiyuki TANAKA,and Yoshikazu SAKAGAMI Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 3 . staphylionoside K C25H44O12 相似度:72% Chemical & Pharmaceutical Bulletin 2005 53(7) 800-807 Staphylionosides A—K: Megastigmane Glucosides from the Leaves of Staphylea bumalda DC. Qian YU,Katsuyoshi MATSUNAMI,Hideaki OTSUKA,and Yoshio TAKEDA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 4 . myrsinionoside E C24H42O11 相似度:72% Chemical & Pharmaceutical Bulletin 2001 49(12) 1558-1566 Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 5 . ficalloside C24H42O11 相似度:72% Natural Product Communications 2011 6 159-162 Chemical Constituents and Antioxidant Activity of Ficus callosa Phan Van Kiem, Nguyen Xuan Cuong, Nguyen Xuan Nhiem, Dan Thi Thuy Hang, Nguyen Hoai Nam, Ninh Khac Ban, Chau Van Minh, Zhou Bing, Hae Dong Jang and Young Ho Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 6 . staphylionoside K 相似度:72% Acta Pharmaceutica Sinica 2010 45 1527-1532 Two new phenolic glycosides from the stems of Clematis parviloba YAN Li-hua, XU Li-zhen *, WANG Zhi-min, ZHANG Qi-wei, YANG Shi-lin * Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 7 . foliasalacioside E2 C24H42O11 相似度:68% Chemical & Pharmaceutical Bulletin 2008 56(4) 547-553 Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 8 . foliasalacioside E3 C24H42O11 相似度:68% Chemical & Pharmaceutical Bulletin 2008 56(4) 547-553 Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 9 . foliasalacioside F C24H42O11 相似度:68% Chemical & Pharmaceutical Bulletin 2008 56(4) 547-553 Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 10 . platanionoside H C24H42H11 相似度:68% Chemical & Pharmaceutical Bulletin 2002 50(3) 390-394 Platanionosides D—J: Megastigmane Glycosides from the Leaves of Alangium platanifolium (SIEB. et ZUCC.) HARMS var. platanifolium SIEB. et ZUCC. Hideaki OTSUKA and Akie TAMAKI Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 11 . foliasalacioside E1 C24H42O11 相似度:64% Chemical & Pharmaceutical Bulletin 2008 56(4) 547-553 Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 12 . foliasalacioside I C24H42O11 相似度:64% Chemical & Pharmaceutical Bulletin 2008 56(4) 547-553 Absolute Structures of New Megastigmane Glycosides, Foliasalaciosides E1, E2, E3, F, G, H, and I from the Leaves of Salacia chinensis Yi ZHANG, Seikou NAKAMURA, Yutana PONGPIRIYADACHA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 13 . Linarionoside C C25H44O12 相似度:64% Phytochemistry 1994 37 461-465 Linarionosides A–C and acyclic monoterpene diglucosides from Linaria japonica Hideaki Otsuka Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 14 . linarionoside C 相似度:64% Acta Pharmaceutica Sinica 2010 45 1527-1532 Two new phenolic glycosides from the stems of Clematis parviloba YAN Li-hua, XU Li-zhen *, WANG Zhi-min, ZHANG Qi-wei, YANG Shi-lin * Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 15 . 2β,3β,20R,22R,25-Pentahydroxy-5β-cholest-6,8(14)-dien C27H44O5 相似度:59.2% Steroids 2007 72 751-755 Three new steroids from the roots of Serratula wolffii András Simon, Gábor Tóth, Erika Liktor-Busa, Zoltán Kele, Mária Takács, András Gergely, Mária Báthori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 16 . (2β,3α,5β,14β,22R)- 2,3,20,22,25-pentahydroxycholest-7-en-6-one C27H44O6 相似度:57.6% Helvetica Chimica Acta 2008 Vol. 91 1640 Additional Minor Phytoecdysteroids of Serratula wolffii András Simon, Erika Liktor-Busa, Gábor To´ th, Zoltán Kele, Judit Groska, and Mária Báthorió Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 17 . ent-14-labden-8β,13α-diol 19-O-β-D-glucopyranoside C26H46O8 相似度:57.6% Journal of Natural Products 2007 70 1837-1845 Diterpenoid Glycosides from the Bitter Fern Gleichenia quadripartita Cecilia Socolsky,Yoshinori Asakawa,and Alicia Bardón Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 18 . hymatoxin K C26H40O9 相似度:57.6% Natural Product Research 1995 6 37-42 Hymatoxins K and L, Novel Phytotoxins from Hypoxylon mammatum, Fungal Pathogen of Aspens Akino Jossang; Bodnem Mbeminack; Jean Pinon; Bernard Bodo Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 19 . gomojoside K C26H44O8 相似度:57.6% Phytochemistry 1993 32 1515-1518 Diterpene glucosides from Viburnum suspensum Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 20 . gomojoside L C26H46O8 相似度:57.6% Phytochemistry 1993 32 1515-1518 Diterpene glucosides from Viburnum suspensum Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 21 . gomojoside Q C26H42O8 相似度:57.6% Phytochemistry 1993 32 1515-1518 Diterpene glucosides from Viburnum suspensum Tetsuo Iwagawa, Shigetoshi Yaguchi, Tsunao Hase, Tsutomu Okubo, Mujo Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 22 . (4R,13S)-18-O-β-Dglucopyranosyllabda-8(17),14-dien-13-ol C26H44O7 相似度:57.6% Helvetica Chimica Acta 2011 94 1085-1090 Diterpenoids from Diplopterygium rufopilosum Jiang Hu, Xuan-Qin Chen, and Qin-Shi Zhao Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 23 . 2β,15S,16,17,19-pentahydroxy-isopimar-8(14)-ene 17-O-β-D-glucopyranoside C26H44O10 相似度:57.6% Phytochemistry 2012 76 172-177 Diterpenes,ionol-derived,and flavone glycosides from Podocarpus elongatus Laura Faiella,Abeer Temraz,Nunziatina De Tommasi,Alessandra Braca Structure 13C NMR 碳谱模拟图 |

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