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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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小白_世界: 金币+10 2013-09-26 15:11:37
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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