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swj19900601金虫 (正式写手)
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溶剂:氘代氯仿 碳谱数据:14.0,16.7,18.0,18.3,19.3,19.6,19.7,20.0,21.1,22.5,22.6,22.7,24.4,24.8,25.4,26.0,26.1,26.4,28.0,28.1,29.9,30.0,30.3,31.9,32.7,32.8,35.5,36.3,36.9,37.3,37.3,38.8,39.0,39.3,40.4,45.3,47.1,47.9,48.8,52.0,61.4,61.5,62.7,70.7,76.8,77.0,77.2,78.8,125.6,139.3 |
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铁杆木虫 (著名写手)
- 应助: 1216 (讲师)
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- 专业: 天然有机化学
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swj19900601: 金币+5 2013-12-20 12:44:28
感谢参与,应助指数 +1
swj19900601: 金币+5 2013-12-20 12:44:28
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查询结果:共查到3178个化合物(查询结果仅供参考) 1 . compound 9 C60H987O2 相似度:72% Chemical & Pharmaceutical Bulletin 1992 40 1773-1778 Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA Structure 13C NMR 碳谱模拟图 2 . Sinocalycanchinensin C C49H82O4 相似度:70% Bioorganic & Medicinal Chemistry 2011 19 2790-2796 New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis Yoshiki Kashiwada , Kazuya Nishimura, Shin-ichiro Kurimoto, Yoshihisa Takaishi Structure 13C NMR 碳谱模拟图 3 . codonopilate A C49H82O3 相似度:68% Journal of Natural Medicines 2011 65 18-23 Three new triterpenyl esters, codonopilates A–C, isolated from Codonopsis pilosula Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda Structure 13C NMR 碳谱模拟图 4 . (1R,3aR,4RS,5S,7aR)-1-((R)-1,5-dimethylhexyl)-5-(2,3-dimethylphenylamino)-3a,7a-dimethyl-octahydroinden-4-ol 相似度:66.6% Bioorganic & Medicinal Chemistry 2013 21 1925-1943 Stereoselective synthesis of a new class of potent and selective inhibitors of human Δ8,7-sterol isomerase Mathias König, Christoph Müller, Franz Bracher Structure 13C NMR 碳谱模拟图 5 . eryloside F5 C46H77O14 相似度:66% Journal of Natural Products 2007 70 1871-1877 Isolation and Structures of Erylosides from the Carribean Sponge Erylus goffrilleri Shamil Sh. Afiyatullov,Anatoly I. Kalinovsky, Alexandr S. Antonov, Ludmila P. Ponomarenko, Pavel S. Dmitrenok,Dmitry L. Aminin, Vladimir B. Krasokhin, Valentina M. Nosova, and Alexandr V. Kisin Structure 13C NMR 碳谱模拟图 6 . eryloside V C48H80C17 相似度:66% Journal of Natural Products 2007 70 1871-1877 Isolation and Structures of Erylosides from the Carribean Sponge Erylus goffrilleri Shamil Sh. Afiyatullov,Anatoly I. Kalinovsky, Alexandr S. Antonov, Ludmila P. Ponomarenko, Pavel S. Dmitrenok,Dmitry L. Aminin, Vladimir B. Krasokhin, Valentina M. Nosova, and Alexandr V. Kisin Structure 13C NMR 碳谱模拟图 7 . 5,6β-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate C59H112O5Si2 相似度:66% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoudé-Werner, Michel Miesch Structure 13C NMR 碳谱模拟图 8 . codonopilate B C49H82O3 相似度:66% Journal of Natural Medicines 2011 65 18-23 Three new triterpenyl esters, codonopilates A–C, isolated from Codonopsis pilosula Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda Structure 13C NMR 碳谱模拟图 9 . skimmiarepin A 相似度:65.3% Phytochemistry 1994 36 1303-1306 Protolimonoid and lignans from Zanthoxylum petiolare Mara S.P. Arruda, João B. Fernandes, Paulo C. Vieira, M. Fatima Das G.F. Da Silva, Jose R. Pirani Structure 13C NMR 碳谱模拟图 10 . 29-norcycloart-5-ene and 5,8-lanostadiene-3β-ol 相似度:65.3% Zeitschrift für Naturforschung C 2004 59 15-18 Chemical Constituents of Euphorbia marschalliana Boiss. A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara Structure 13C NMR 碳谱模拟图 11 . compound 6 相似度:64% Chemical & Pharmaceutical Bulletin 1992 40 1773-1778 Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA Structure 13C NMR 碳谱模拟图 12 . 7-Ketocholesteryl-9,10-di-tertbutyldimethylsilyloxystearate C57H106O5Si2 相似度:64% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoudé-Werner, Michel Miesch Structure 13C NMR 碳谱模拟图 |
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