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| 16.1, 19.5, 19.8, 26.8, 27.9, 28.6, 28.6, 30.3, 32.7, 34.9, 35.7, 39.8, 40.3, 58.7, 60.3, 81.6, 116.1, 119.9, 122.9, 126.9, 136.9, 137.0, 143.3, 171.1, 172.4 |
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专家经验: +726 - PhEPI: 3
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三寸日光1234: 金币+10 2013-11-28 20:25:37
感谢参与，应助指数 +1
三寸日光1234: 金币+10 2013-11-28 20:25:37
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查询模式：模糊查询 碳谱数据输入： 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 溶剂选项： 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270个化合物(查询结果仅供参考) 1 . Z-neomanoalide 相似度:96% Journal of Natural Products 1992 Vol 55 174 Four New Antibacterial Sesterterpenes from a Marine Sponge of the Genus Luffariella Gabriele M. König, Anthony D. Wright, Otto Sticher Structure 13C NMR 碳谱模拟图 2 . (Z)-neomanoalide 相似度:92% Chemical & Pharmaceutical Bulletin 1994 42 265-270 Marine Natural Products. XXXII. Absolute Configurations of C-4 of the Manoalide Family, Biologically Active Sesterterpenes from the Marine Sponge Hyrtions erecta Motomasa KOBAYASHI,Takumi OKAMOTO,Kozo HAYASHI,Norio YOKOYAMA,Takuma SASAKI and Isao KITAGAWA Structure 13C NMR 碳谱模拟图 3 . (Z)-neomanoalide C25H38O4 相似度:92% Tetrahedron letters 1981 22 3147-3150 Three new sesterterpenoid antibiotics from the marine sponge Luffariella variabilis (polejaff) E.Dilip de Silva, Paul J. Scheuer Structure 13C NMR 碳谱模拟图 4 . (6Z)-Neomanoalide 相似度:92% The Journal of Organic Chemistry 1992 57 3503-3507 Luffariolides A-E, new cytotoxic sesterterpenes from the Okinawan marine sponge Luffariella sp Masashi Tsuda, Hideyuki Shigemori, Masami Ishibashi, Takuma Sasaki, Junichi Kobayashi Structure 13C NMR 碳谱模拟图 5 . (E)-neomanoalide C25H38O4 相似度:84% Tetrahedron letters 1981 22 3147-3150 Three new sesterterpenoid antibiotics from the marine sponge Luffariella variabilis (polejaff) E.Dilip de Silva, Paul J. Scheuer Structure 13C NMR 碳谱模拟图 6 . (6E)-Neomanoalide 相似度:84% The Journal of Organic Chemistry 1992 57 3503-3507 Luffariolides A-E, new cytotoxic sesterterpenes from the Okinawan marine sponge Luffariella sp Masashi Tsuda, Hideyuki Shigemori, Masami Ishibashi, Takuma Sasaki, Junichi Kobayashi Structure 13C NMR 碳谱模拟图 7 . Z-24-acetoxyneomandide C27H42O5 相似度:81.4% Journal of Natural Products 1992 Vol 55 174 Four New Antibacterial Sesterterpenes from a Marine Sponge of the Genus Luffariella Gabriele M. König, Anthony D. Wright, Otto Sticher Structure 13C NMR 碳谱模拟图 8 . (E)-neomanoalide 相似度:80% Chemical & Pharmaceutical Bulletin 1994 42 265-270 Marine Natural Products. XXXII. Absolute Configurations of C-4 of the Manoalide Family, Biologically Active Sesterterpenes from the Marine Sponge Hyrtions erecta Motomasa KOBAYASHI,Takumi OKAMOTO,Kozo HAYASHI,Norio YOKOYAMA,Takuma SASAKI and Isao KITAGAWA Structure 13C NMR 碳谱模拟图 9 . lurrariolide F C25H38O5 相似度:80% Journal of Natural Products 1993 Vol 56 436 Luffariolides F and G, New Manoalide Derivatives from the Okinawan Marine Sponge Luffariella Sp. Jun'ichi Kobayashi, Chun-min Zeng, Masami Ishibashi, Takuma Sasaki Structure 13C NMR 碳谱模拟图 10 . lurrariolide G C25H38O5 相似度:76% Journal of Natural Products 1993 Vol 56 436 Luffariolides F and G, New Manoalide Derivatives from the Okinawan Marine Sponge Luffariella Sp. Jun'ichi Kobayashi, Chun-min Zeng, Masami Ishibashi, Takuma Sasaki Structure 13C NMR 碳谱模拟图 11 . deoxysecomanoalide C25H34O3 相似度:76% Chemical & Pharmaceutical Bulletin 2009 57 885-887 Deoxymanoalides from the Nudibranch Chromodoris willani Mohammad Helal Uddin, Masahito Otsuka, Toshinobu Muroi, Atsushi Ono, Novriyandi Hanif, Seiko Matsuda, Tatsuo Higa and Junichi Tanaka Structure 13C NMR 碳谱模拟图 12 . Luffariolide B C25H38O4 相似度:76% The Journal of Organic Chemistry 1992 57 3503-3507 Luffariolides A-E, new cytotoxic sesterterpenes from the Okinawan marine sponge Luffariella sp Masashi Tsuda, Hideyuki Shigemori, Masami Ishibashi, Takuma Sasaki, Junichi Kobayashi Structure 13C NMR 碳谱模拟图 |
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