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微谱数据库求助
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| 11.99,15.38,15.44,17.57,18.26,18.71,18.79,18.90,19.21,19.85,20.23,20.55,26.01,30.25,30.55,31.44,32.43,33.70,33.92,35.75,38.82,39.05,45.80 |
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jasminelw
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小白_世界: 金币+10 2013-09-26 15:11:37
感谢参与，应助指数 +1
小白_世界: 金币+10 2013-09-26 15:11:37
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查询结果：共查到7535个化合物(查询结果仅供参考) 1 . (3RS,5RS,8RS)-4-[ (2H3)Methyl]-4,5,8-trimethyl-1-oxaspiro[2.5]octane 相似度:78.2% Helvetica Chimica Acta 2009 92 1782-1799 Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification Christian Chapuis, Carole Cantatore, Peter Fankhauser, René Challand, Jean-Jacques Riedhauser Structure 13C NMR 碳谱模拟图 2 . Geosmin 相似度:78.2% Phytochemistry 1977 16 2025-2027 The carbon-13 nuclear magnetic resonance spectra of four eudesmane sesquiterpenols Nancy N. Gerber, Dorothy Z. Denney Structure 13C NMR 碳谱模拟图 3 . (3R,5R,9R)-3,5,9-trimethyldodecyl-(1'R)-trans-chrysan-themate 相似度:75% Journal of Chemical Ecology 2012 38 1493-1503 First Sex Pheromone of the Order Strepsiptera: (3R,5R,9R)-3,5,9-Trimethyldodecanal in Stylops melittae KIRBY, 1802 Till Tolasch & Siegfried Kehl & Stefan Dötterl Structure 13C NMR 碳谱模拟图 4 . (2R/S,6R/S,10R/S)-methyl-2,6,10-trimethyltridecanoate 相似度:73.9% Journal of Chemical Ecology 2000 26 2737-2746 Synthesis and Biological Activity of Methyl 2,6,10-Trimethyldodecanoate and Methyl 2,6,10-Trimethyltridecanoate: Male-Produced Sexual Pheromones of Stink Bugs Euschistus heros and Piezodorus guildinii Paulo H. G. Zarbin, Aurélia Reckziegel, Ernst Plass, Miguel Borges, Wittko Francke Structure 13C NMR 碳谱模拟图 5 . 3-epi-betulinic acid 3-O-sulfate 相似度:72% Phytotherapy Research 2007 21 466-470 Antiviral triterpenoids from the medicinal plant Schefflera heptaphylla Yaolan Li, Renwang Jiang, Linda S. M. Ooi, Paul P. H. But and Vincent E. C. Ooi Structure 13C NMR 碳谱模拟图 6 . 3α,15-diacetoxy-neo-clerodane 相似度:70.8% Tetrahedron 1994 50 10791-10802 Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jiménez, Anna M. Lithgow, Margarita López, Rosalina F. Moro, Antonio Gómez Structure 13C NMR 碳谱模拟图 7 . compound 相似度:70.8% Tetrahedron 2012 68 4995-5004 Synthetic routes to campesterol and dihydrobrassicasterol: a first reported synthesis of the key phytosterol dihydrobrassicasterol N.M. O'Connell, Y.C. O'Callaghan, N.M. O'Brien, A.R. Maguire, F.O. McCarthy Structure 13C NMR 碳谱模拟图 8 . Mycaperoxide A C24H42O5 相似度:70.8% The Journal of Organic Chemistry 1993 58 2999-3002 Bioactive norsesterterpene 1,2-dioxanes from a Thai sponge, Mycale sp Junichi Tanaka, Tatsuo Higa, Khanit Suwanborirux, Udom Kokpol, Gerald Bernardinelli, Charles W. Jefford Structure 13C NMR 碳谱模拟图 9 . 5-acetoxy-cis-clerodan-3-ene-18-oic acid C22H36O4 相似度:69.5% Journal of Natural Products 2003 66 316-319 cis-Clerodane Type Diterpenes from Cistus monspeliensis1 Eleftherios Kalpoutzakis, Nektarios Aligiannis, Alexios-Leandros Skaltsounis, and Sofia Mitakou Structure 13C NMR 碳谱模拟图 10 . 15-acetoxy-cis-clerodan-3-ene-18-al C22H36O3 相似度:69.5% Journal of Natural Products 2003 66 316-319 cis-Clerodane Type Diterpenes from Cistus monspeliensis1 Eleftherios Kalpoutzakis, Nektarios Aligiannis, Alexios-Leandros Skaltsounis, and Sofia Mitakou Structure 13C NMR 碳谱模拟图 11 . octanor-13β-dammarane 相似度:69.5% Chemistry of Natural Compounds 1982 18 560-564 PARTIAL SYNTHESIS OF OCTANOR-13β-DAMMARANE G. V. Malinovskaya, N. D. Pokhilo, V. L. Novikov, V. A. Denisenko, and N. I. Uvarova Structure 13C NMR 碳谱模拟图 12 . (13S,17R)-17-Acetoxy-6β-methoxy-3α,5-cyclo-13,14-seco-5α-androstane 相似度:69.5% Steroids 2004 69 501-509 Synthesis of 13,14-secotestosterone derivatives Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Yuliya Y. Zhiburtovich, Galina P. Fando, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR 碳谱模拟图 13 . O3-[(1,1-Dimethylethyl)dimethylsilanyl]epiandrosteron 相似度:69.5% Steroids 2005 70 103-110 First synthesis of a pentadeuterated 3′-hydroxystanozolol—an internal standard in doping analysis Wolfgang Felzmann, Günter Gmeiner, Peter Gärtner Structure 13C NMR 碳谱模拟图 14 . octanordammarane 相似度:69.5% Phytochemistry 1998 49 2461-2466 Dammarane triterpenoids from rhizomes of Pyrrosia lingua Hiroshi Yamashita, Kazuo Masuda, Tomomi Kobayashi, Hiroyuki Ageta, Keniji Shiojima Structure 13C NMR 碳谱模拟图 15 . compound 8 C22H36O4 相似度:69.5% Phytochemistry 1994 35 721-724 Ent-labdane and neo-clerodane diterpenes from Gymnosperma glutinosum Emma Maldonado, Rosabel Segura-Correa, Alfredo Ortega, José S. Calderón, Frank R. Fronczek Structure 13C NMR 碳谱模拟图 16 . Dihydro-α-santalol 相似度:69.5% Molecules 2012 17 2259-2270 Structure-Odor Relationships of α-Santalol Derivatives with Modified Side Chains Toshio Hasegawa , Hiroaki Izumi , Yuji Tajima and Hideo Yamada Structure 13C NMR 碳谱模拟图 17 . Dihydro-α-santalyl formate C16H26O2 相似度:69.5% Molecules 2012 17 2259-2270 Structure-Odor Relationships of α-Santalol Derivatives with Modified Side Chains Toshio Hasegawa , Hiroaki Izumi , Yuji Tajima and Hideo Yamada Structure 13C NMR 碳谱模拟图 18 . 15-acetoxy-neo-clerodan-3β-ol 相似度:69.5% Tetrahedron 1994 50 10791-10802 Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jiménez, Anna M. Lithgow, Margarita López, Rosalina F. Moro, Antonio Gómez Structure 13C NMR 碳谱模拟图 19 . 15-acetoxy-8,9-epoxylabdane-19-oic acid C22H36O5 相似度:69.5% Zeitschrift für Naturforschung C 2005 60 511-522 Gastroprotective Effect and Cytotoxicity of Natural and Semisynthetic Labdane Diterpenes from Araucaria araucana Resin G. Schmeda-Hirschmann, L. Astudillo, B. Sepúlveda, J. A. Rodríguez, C. Theoduloz, T. Yáñez, and J. A. Palenzuela Structure 13C NMR 碳谱模拟图 20 . [(1R,3aS,4R,7aR)-1-((R)-1,5-dimethylhexyl)-7a-methylhexahydrocyclopropa[d]inden-4-yl-oxy]-trimethylsilane 相似度:69.5% 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 21 . 2,4,6,8-tetramethylundecan-1-ol 相似度:69.5% The Journal of Organic Chemistry 2005 70 1808-1827 Novel Cuticular Hydrocarbons from the Cane Beetle Antitrogus parvuluss4,6,8,10,16-Penta- and 4,6,8,10,16,18-HexamethyldocosanessUnprecedented anti-anti-anti-Stereochemistry in the 4,6,8,10-Methyltetrad Sharon Chow, Mary T. Fletcher, Lynette K. Lambert, Oliver P. Gallagher, Christopher J. Moore, Bronwen W. Cribb, Peter G. Allsopp, and William Kitching Structure 13C NMR 碳谱模拟图 22 . Methyl 2,6,10-Trimethyltridecanoate C17H34O2 相似度:69.5% European Journal of Organic Chemistry 1994 1994 637-639 Pheromone Synthesis, CLXII. Synthesis of Methyl 2,6,10-Trimethyltridecanoate, the Male-Produced Pheromone of the Stink Bugs, Euschistus heros and E. obscurus, as a Stereoisomeric Mixture Kenji Mori and Noriaki Murata Structure 13C NMR 碳谱模拟图 23 . 2,5,6-Trimethylheptan-1-ol C10H22O 相似度:69.5% Flavour and Fragrance Journal 2001 16 207-208 Reconstruction of lavandulol carbon skeleton based on limonene. Synthesis of isotetrahydrolavandulol Józef Kula, Janina Wilczyńska and Ilona Chmielecka Structure 13C NMR 碳谱模拟图 24 . isomerictrisnorhopane 相似度:69.2% Chemical & Pharmaceutical Bulletin 1994 42 377-378 Fern Constituent : A New Triterpenoid Hydrocarbon, Trisnorhopane, Isolated from the Leaves of Dryopteris crassirhizoma and Gleichenia japonica Kenji SHIOJIMA,Masayoshi SUZUKI,Tae MATSUMURA and Hiroyuki AGETA Structure 13C NMR 碳谱模拟图 25 . 3β-Methoxy-19,20,21,22,29,30-hexanor-18,19-seco(17βH)lupan-18-one 相似度:68% Chemistry of Natural Compounds 1992 28 179-184 RETRO-MICHAEL REACTION OF 28-METHOXY-18,19-SECOLUPANE-18,19-DIONE DERIVATIVES L. E. Odinokova, M. V. Denisenko, V. A. Denisenko,and N. I. Uvarova Structure 13C NMR 碳谱模拟图 26 . asa-4,6,8,10,16-pentamethyldocosane 相似度:67.8% The Journal of Organic Chemistry 2005 70 1808-1827 Novel Cuticular Hydrocarbons from the Cane Beetle Antitrogus parvuluss4,6,8,10,16-Penta- and 4,6,8,10,16,18-HexamethyldocosanessUnprecedented anti-anti-anti-Stereochemistry in the 4,6,8,10-Methyltetrad Sharon Chow, Mary T. Fletcher, Lynette K. Lambert, Oliver P. Gallagher, Christopher J. Moore, Bronwen W. Cribb, Peter G. Allsopp, and William Kitching Structure 13C NMR 碳谱模拟图 27 . 16-Methyl-5α-androstane-3β,17-diacetate 5d C24H38O4 相似度:66.6% Steroids 2001 66 833-843 Configurational analysis and relative binding affinities of 16-methyl-5α-androstane derivatives Pál Tapolcsányi, János Wölfling, István Tóth, Mihály Szécsi, Péter Forgó, Gyula Schneider Structure 13C NMR 碳谱模拟图 28 . 16-Methyl-5α-androstane-3β,17-diacetate 8d C24H38O4 相似度:66.6% Steroids 2001 66 833-843 Configurational analysis and relative binding affinities of 16-methyl-5α-androstane derivatives Pál Tapolcsányi, János Wölfling, István Tóth, Mihály Szécsi, Péter Forgó, Gyula Schneider Structure 13C NMR 碳谱模拟图 29 . (18R)-pyrrosialactone 相似度:66.6% Phytochemistry 1998 49 2461-2466 Dammarane triterpenoids from rhizomes of Pyrrosia lingua Hiroshi Yamashita, Kazuo Masuda, Tomomi Kobayashi, Hiroyuki Ageta, Keniji Shiojima Structure 13C NMR 碳谱模拟图 30 . 24,26-cyclo-5α-cholest-(22E)-en-3β-ol C27H44O 相似度:66.6% Journal of Natural Products 1991 Vol 54 1119 New Sterol Ester from a Deep Water Marine Sponge, Xestospongia sp. Sarath P. Gunasekera, Susan Cranick, Shirley A. Pomponi Structure 13C NMR 碳谱模拟图 |
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