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IMB001

金虫 (小有名气)

[求助] 一个化合物微谱求助

碳谱数据:13.0, 20.9,27.2, 30.4, 31.3, 31.6, 39.0, 44.1, 49.1, 50.0, 52.9, 53.4, 70.5, 106.1, 107.1, 114.9, 126.9, 128.6, 128.8, 129.1, 134.6, 137.6, 147.6, 153.1, 156.1,174.5
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潘宪伟

木虫 (正式写手)

【答案】应助回帖

★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
karl2100: 金币+1, 3Q 2013-03-13 00:04:45
IMB001: 金币+20 2013-03-13 19:32:34
查询结果:共查到217个化合物(查询结果仅供参考)  
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1 .     O-[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]oestrone
C28H31N3O2     相似度:65.3%
Heterocycles          2012          84          1033-1044
Multicomponent Click Synthesis of Potentially Biologically Active Triazoles Catalysed by Copper Nanoparticles on Activated Carbon in Water
Francisco Alonso,* Yanina Moglie, Gabriel Radivoy, and Miguel Yus
Structure      13C NMR   碳谱模拟图

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2 .     22-oxa-(12)-cytochalasa-6(12),13,19-triene-1,21-dione-7,18-dihydroxy-16,18-dimethyl-10-phenyl-(7S*,13E,16S*,18S*,19E)
C28H35NO5     相似度:61.5%
Phytochemistry          1996          41          821-828
Cytochalasins from a Daldinia sp. of fungus
Malcolm S. Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa
Structure      13C NMR   碳谱模拟图

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3 .     cytochalasin H
    相似度:60.7%
Journal of Agricultural and Food Chemistry          1983          31          405-408
Proton and carbon-13 nuclear magnetic resonance studies of the conformation of cytochalasin H derivatives and plant growth regulating effects of cytochalasins
Richard H. Cox, Philip Morris, Horace G. Cutler, Ralph E. Hurd, Richard J. Cole
Structure      13C NMR   碳谱模拟图

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4 .     3-Benzyloxyestra-1,3,5(10)-trien-17-one
C25H28O2     相似度:57.6%
Steroids          2002          67          371-377
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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5 .     3-Benzyloxyestra-1,3,5(10)-trien-17-one
C25H28O2     相似度:57.6%
Steroids          2002          67          671-678
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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6 .     3-Benzyloxy-16β-bromomethylestra-1,3,5(10)-trien-17β-yl acetate
C28H33O3Br     相似度:57.6%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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7 .     3-Benzyloxy-16α-bromomethylestra-1,3,5(10)-trien-17α-yl acetate
C28H33O3Br     相似度:57.6%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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8 .     16β-Acetoxymethyl-3-benzyloxy-17-methyl-18-nor-estra-1,3,5(10),13(17)-tetraene
C28H32O3     相似度:57.6%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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9 .     3-benzyloxy-16-bromomethylestra-1,3,5(10)-trien-17-ol 8a
C26H31O2Br     相似度:57.6%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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10 .     3-Benzyloxy-16-bromomethylestra-1,3,5(10)-trien-17-yl acetate 8b
C28H33O3Br     相似度:57.6%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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11 .     3-benzyloxy-1,3,5(10)-estratrien-17-one
C25H28O2     相似度:57.6%
Steroids          2006          71          911-921
Synthesis of unique 17β-estradiol homo-dimers, estrogen receptors binding affinity evaluation and cytocidal activity on breast, intestinal and skin cancer cell lines
Gervais Bérubé, Daniel Rabouin, Valérie Perron, Blaise N’Zemba, René-C. Gaudreault, Sophie Parent, éric Asselin
Structure      13C NMR   碳谱模拟图

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12 .     (11)-cytochalasa-6(12),13-diene-1,21-dione-16,18-dimethyl-7-hydroxy-10-phenyl-(7S*,13E,16S*,18S*)
C28H37NO3     相似度:57.6%
Phytochemistry          1996          41          821-828
Cytochalasins from a Daldinia sp. of fungus
Malcolm S. Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa
Structure      13C NMR   碳谱模拟图

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13 .     [11]-cytochalasa-6(12),13-diene-1,21-dione-7,18-dihydroxy-16,18-dimethyl-10-phenyl-(7S*,13E,16S*,18R*)
C28H37O4N     相似度:57.6%
Phytochemistry          1995          40          135-140
Five 10-phenyl-[11]-cytochalasans from a Daldinia fungal species
Malcolm Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa
Structure      13C NMR   碳谱模拟图

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14 .     benzyl11β,17α-dihydroxy-3-oxoandrosta-1,4-diene-17βcarboxylate
C30H36O7     相似度:57.6%
Steroids          1996          61          524-530
Structural studies of loteprednol etabonate and other analogs of prednisolone using NMR techniques
Stanislaw Rachwal, Emil Pop, Marcus E. Brewster
Structure      13C NMR   碳谱模拟图

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15 .     4-(3'-ethyl-4'-hydroxy-3-methyl-biphenyl)-4-oxo-N-pyridin-3-ylethyl-butyramide
C26H28N2O3     相似度:57.6%
Bioorganic & Medicinal Chemistry          2008          16          4438-4456
Novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1: Templates for design
Gillian M. Allan, Nigel Vicker, Harshani R. Lawrence, Helena J. Tutill, Joanna M. Day, Marion Huchet, Eric Ferrandis, Michael J. Reed, Atul Purohit, Barry V.L. Potter
Structure      13C NMR   碳谱模拟图

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16 .     (2R)-N-{(3R)-3-[4-(benzyloxy)phenyl]pentanoyl}bornane-10,2-sultam
C28H35NO4S     相似度:57.6%
Helvetica Chimica Acta          2011          94          2141-2167
Diastereoselective Alkyl Grignard 1,4-Additions to para-Substituted (2R)-N-Cinnamoylbornane-10,2-sultam Derivatives: Influence of N-Atom Pyramidalization (pages 2141–2167)
Anna M. Piątek, Agnieszka Sadowska, Christian Chapuis and Janusz Jurczak
Structure      13C NMR   碳谱模拟图

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17 .     cytochalasin D
    相似度:57.1%
Helvetica Chimica Acta          2002          Vol. 85          1439
Neoengleromycin, a Novel Compound from Engleromyces goetzii
Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui
Structure      13C NMR   碳谱模拟图

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18 .     Cytochalasin D
    相似度:57.1%
Chinese Journal of Marine Drugs          2011          30(1)          15-17
Chemical constituents of mangrove plant Bruguiera gymnorrhiza
CAI You-sheng, LIU Hai-li, GONG Jing-xu, GUO Yue-wei
Structure      13C NMR   碳谱模拟图

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19 .     cytochalasin H
    相似度:57.1%
Tetrahedron          1989          45          2323-2335
Six new 10-pheynl-[11]cytochalasans, cytochalasins N - S from phomopsis SP.
Yoshihiko Izawa, Takashi Hirose, Takako Shimizu (née Tomioka), Kiyotaka Koyama, Shinsaku Natori
Structure      13C NMR   碳谱模拟图

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20 .     17β-estradiol-3-benzyl ether 17-tosylate
C32H36O4S     相似度:55.5%
Steroids          2011          76          1141-1148
Synthesis of novel steroidal 17 -triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro
éva Frank∗, Judit Molnár, István Zupkó, Zalán Kádár, János Wölfling
Structure      13C NMR   碳谱模拟图

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21 .     16-Hydroxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-ol isomer 5a
C26H32O3     相似度:53.8%
Steroids          2002          67          371-377
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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22 .     16 α-Acetoxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-one
C28H32O4     相似度:53.8%
Steroids          2002          67          371-377
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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23 .     16-Hydroxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-ol isomer 5a
C26H32O3     相似度:53.8%
Steroids          2002          67          671-678
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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24 .     16 α-Acetoxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-one
C28H32O4     相似度:53.8%
Steroids          2002          67          671-678
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
Pál Tapolcsányi, János Wölfling, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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25 .     3-Benzyloxy-16α-acetoxymethyl-13α-estra-1,3,5(10)-trien-17β-ol
C28H34O4     相似度:53.8%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
János Wölfling, Erzsébet Mernyák, éva Frank, George Falkay, árpád Márki, Renáta Minorics, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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26 .     1' ,4' ,16,17-tetrahydro-3β-hydroxy-6' -bromo-4' -methyl-(16α,17α)-androsta-5,16-dieno[17,16-b]quinoline
C27H36BrNO     相似度:53.8%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Angéla Magyar, János Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, Péter Forgó, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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27 .     3-benzyloxy-16β-acetoxymethylestra-1,3,5(10)-trien-17β-yl acetate
C30H36O5     相似度:53.8%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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28 .     3-benzyloxy-16β-hydroxymethylestra-1,3,5(10),13(17)-tetraene
C26H30O2     相似度:53.8%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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29 .     3-benzyloxy-16-bromomethylestra-1,3,5(10)-trien-17-ol 5a
C26H31O2Br     相似度:53.8%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图

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30 .     3-Benzyloxy-16-bromomethylestra-1,3,5(10)-trien-17-yl acetate 7b
C28H33O3Br     相似度:53.8%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, árpád Márki, George Falkay, Gyula Schneider
Structure      13C NMR   碳谱模拟图
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