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liuxiaosa

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10.8,12.0,13.0,14.0,19.1,21.6,23.8,24.2,28.1,30.2,30.5,31.6,34.0,34.2,34.7,45.8,47.2,58.3,64.2,67.0,108.7,123.1,127.0,134.1,
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fu_jian2008

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liuxiaosa: 金币+10, ★★★很有帮助 2013-06-13 21:43:57
liuxiaosa(豆哥代发): 金币+10, 谢谢 2013-06-24 08:59:48
1 .     Bis(17-oxo-5α-androstan[2,3-b:2',3'-e])pyrazine
C38H52N2O2     相似度:66.6%
Journal of Natural Products          2012          75          1063-1069
The Cephalostatins. 22. Synthesis of Bis-steroidal Pyrazine Pyrones
George R. Pettit, Bryan R. Moser, Ricardo F. Mendonça, John C. Knight, and Fiona Hogan
Structure      13C NMR   碳谱模拟图

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2 .     17β-(Ureylene-N-cyclopropyl-N'-butyl)-4-methyl-4-aza-5α-androst-1-ene-3-one
C27H43N3O2     相似度:62.9%
Bioorganic & Medicinal Chemistry          1997          5          305-310
Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
Mettilda Lourdusamy, Jean Côté, S. Laplante, Fernand Labrie, Shankar M. Singh
Structure      13C NMR   碳谱模拟图

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3 .     17β-(Ureylene-N-cyclopropyl-N'-isopropyl)-4-methyl-4-aza-5α-androst-1-ene-3-one
C26H41N3O2     相似度:62.5%
Bioorganic & Medicinal Chemistry          1997          5          305-310
Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
Mettilda Lourdusamy, Jean Côté, S. Laplante, Fernand Labrie, Shankar M. Singh
Structure      13C NMR   碳谱模拟图

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4 .     delta-9-tetrahydro cannabinol
    相似度:62.5%
Natural Product Research and Development          2011          23          82-84
Analysis of Cannabinoids from Leaves of Ancient Cannabis sativa Found in Yanghai Xinjiang,China
MA Qing-yun; JIANG Hong-en; ZHAO You-xing
Structure      13C NMR   碳谱模拟图

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5 .     sinulobatin C
C22H32O3     相似度:62.5%
Tetrahedron          1997          53          4569-4578
Sinulobatins A-D, new amphilectane-type diterpenoids from the Japanese soft coral Sinularia nanolobata
Koji Yamada, Tami Ujiie, Katsumi Yoshida, Tomofumi Miyamoto, Ryuichi Higuchi
Structure      13C NMR   碳谱模拟图

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6 .     17β-(Ureylene-N-cyclopropyl-N'-ethyl)-4-methyl-4-aza-5α-androst-1-ene-3-one
C25H39N3O2     相似度:60%
Bioorganic & Medicinal Chemistry          1997          5          305-310
Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
Mettilda Lourdusamy, Jean Côté, S. Laplante, Fernand Labrie, Shankar M. Singh
Structure      13C NMR   碳谱模拟图

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7 .     17β-(Ureylene-N-cyclopropyl-N'-propyl)-4-methyl-4-aza-5α-androst-1-ene-3-one
C26H41N3O2     相似度:60%
Bioorganic & Medicinal Chemistry          1997          5          305-310
Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
Mettilda Lourdusamy, Jean Côté, S. Laplante, Fernand Labrie, Shankar M. Singh
Structure      13C NMR   碳谱模拟图

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8 .     3-(N,N-pentan-1,5-diylcarboxamido)-androst-2,4-diene-17-(ethylene ketal)
    相似度:59.2%
Steroids          2011          76          280-290
Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation
Péter Ács, Attila Takács, Mercédesz Kiss, Noémi Pálinkás, Sándor Mahó, László Kollár
Structure      13C NMR   碳谱模拟图

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9 .     malyngamide C
C24H38ClNO5     相似度:58.3%
Journal of Natural Products          2010          73          463-466
Isolation and Biological Evaluation of 8-epi-Malyngamide C from the Floridian Marine Cyanobacterium Lyngbya majuscula
Jason C. Kwan, Max Teplitski, Sarath P. Gunasekera, Valerie J. Paul and Hendrik Luesch
Structure      13C NMR   碳谱模拟图

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10 .     17β-hydroxy-4-androsteno[3,2-d]-2'-amino-6'-ethoxypyrimidine
    相似度:58.3%
Indian Journal of Chemistry          2006          45B          959-966
A facile synthesis of steroidal pyrazoles,isoxazoles and pyrimidines from testosterone
Singh,Ch Brajakishor; Singh,L Warjeet
Structure      13C NMR   碳谱模拟图

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11 .     ∆(9)-tetrahydrocannabinol
    相似度:58.3%
Phytochemical Analysis          2004          15          345-354
NMR assignments of the major cannabinoids and cannabiflavonoids isolated from flowers of Cannabis sativa
Young Hae Choi, Arno Hazekamp, Anja M. G. Peltenburg-Looman, Michel Frédérich, Cornelis Erkelens, Alfons W. M. Lefeber and Robert Verpoorte
Structure      13C NMR   碳谱模拟图

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12 .     3-morcaptopropanoic acid
    相似度:58.3%
Steroids          1989          53          727-738
Synthesis of 11α-hydroxyprogesterone hartens
Hirokazu Yoshida, Shiro Nakai, Fusako Nimbari, Kiyoko Yoshimoto, Tadashi Nishimura
Structure      13C NMR   碳谱模拟图

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13 .     3R-spiro-(3'-(2'',3''-epoxypropyl)-2'-oxo-oxazolidin-5'-yl)-5α-androstan-17-one
C24H35NO4     相似度:58.3%
Journal of Medicinal Chemistry          2002          45          640-653
Synthesis and Optimization of a New Family of Type 3 17β-Hydroxysteroid Dehydrogenase Inhibitors by Parallel Liquid-Phase Chemistry
René Maltais, Van Luu-The, and Donald Poirier
Structure      13C NMR   碳谱模拟图

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14 .     3-(N,N-3-oxapentan-1,5-diylcarboxamido)-androst-3,5-diene-17-(ethylene ketal)
C26H37O4N     相似度:57.6%
Steroids          2011          76          280-290
Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation
Péter Ács, Attila Takács, Mercédesz Kiss, Noémi Pálinkás, Sándor Mahó, László Kollár
Structure      13C NMR   碳谱模拟图

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15 .     17β-(Ureylene-N-cyclopropyl-N'-cyclohexyl)-4-methyl-4-aza-5α-androst-1-ene-3-one
C29H45N3O2     相似度:57.1%
Bioorganic & Medicinal Chemistry          1997          5          305-310
Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
Mettilda Lourdusamy, Jean Côté, S. Laplante, Fernand Labrie, Shankar M. Singh
Structure      13C NMR   碳谱模拟图

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16 .     compound 5
C25H40O4     相似度:56%
Steroids          2010          75          70-76
Unusual oxidative transformations of a steroidal 16α,17α,22-triol
Jacek W. Morzycki, José Oscar H. Pérez-Díaz, Rosa Santillan, Agnieszka Wojtkielewicz
Structure      13C NMR   碳谱模拟图

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17 .     14β-Ethyl-1 7β-( 3-furyl)-14,15-seco-5β-androstane-3β,14β-diol
C25H40O3     相似度:56%
Steroids          1996          61          572-582
Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives
Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni
Structure      13C NMR   碳谱模拟图

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18 .     5α,8β-环二氧麦角甾-6,22二烯一3β醇
C27H42O5     相似度:56%
Chinese Traditional and Herbal Drugs          2006          37          1152-1153
旱生卷柏化学成分研究(Ⅲ)
刘海青;林瑞超;冯芳
Structure      13C NMR   碳谱模拟图

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19 .     3α,12α,16α-trihydroxycholestane
C27H48O3     相似度:55.5%
Journal of Natural Products          2009          72          102-106
Steroids from an Australian Sponge Psammoclema sp.
Ian P. Holland,Adam McCluskey, Jennette A. Sakoff, Jayne Gilbert, Ngoc Chau, Phillip J. Robinson, Cherie A. Motti, Anthony D. Wright, and Ian A. van Altena
Structure      13C NMR   碳谱模拟图

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20 .     (22R)-6β-Methoxy-3α,5-cyclo-27-nor-5α-cholest-23-yn-22-ol
    相似度:55.5%
Chemistry of Natural Compounds          2009          45          647-652
SYNTHESIS OF 28-HOMOBRASSINOSTEROIDSMODIFIED IN THE 26-POSITION
R. P. Litvinovskaya, M. E. Raiman, and V. A. Khripach
Structure      13C NMR   碳谱模拟图

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21 .     (22R,23Z)-6β-Methoxy-3α,5-cyclo-27-nor-5α-cholest-23-en-22-ol
    相似度:55.5%
Chemistry of Natural Compounds          2009          45          647-652
SYNTHESIS OF 28-HOMOBRASSINOSTEROIDSMODIFIED IN THE 26-POSITION
R. P. Litvinovskaya, M. E. Raiman, and V. A. Khripach
Structure      13C NMR   碳谱模拟图

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22 .     deacetoxysolaphyllidine
    相似度:55.5%
Phytochemistry          1988          27          3024-3027
13C NMR spectra of 4-keto steroidal alkaloids
A. Usubillaga
Structure      13C NMR   碳谱模拟图

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23 .     solanudine
    相似度:55.5%
Phytochemistry          1988          27          3031-3032
Solanudine,a steroidal alkaloid from Solanum nudum
A. Usubillaga
Structure      13C NMR   碳谱模拟图

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24 .     dapholdhamine B
C22H35NO3     相似度:54.1%
Journal of Natural Products          2009          72          1325-1327
Dapholdhamines A-D, Alkaloids from Daphniphyllum oldhami
Yu Zhang,Ying-Tong Di, Shu-Zhen Mu, Chun-Shun Li, Qiang Zhang, Cheng-Jian Tan, Zhen Zhang,Xin Fang, and Xiao-Jiang Hao
Structure      13C NMR   碳谱模拟图

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25 .     consorientaline
C22H34NO3     相似度:54.1%
Journal of Natural Products          2001          64          787-789
Norditerpenoid and Diterpenoid Alkaloids from Turkish Consolida orientalis
Filiz Meriçli, Ali H. Meriçli, Ayhan Ulubelen, Haridutt K. Desai, and S. William Pelletier
Structure      13C NMR   碳谱模拟图

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26 .     compound IV
    相似度:54.1%
Chemistry of Natural Compounds          1991          27          566-571
SECONDARY METABOLITES OF Ulocladium chartarum. A AND B - NEW PHYTOTOXINS OF TERPENOID NATURE
S. I. Sviridov, B. S. Ermolinskii,G. A. Belyakova, and V. G. Dzhavakhiya
Structure      13C NMR   碳谱模拟图

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27 .     1α-Acetoxy-4α-methyl-5α-androst-2-en-l7-on
C22H32O3     相似度:54.1%
Helvetica Chimica Acta          1980          63          1562-1581
Steroide und Sexualhormone. 261. Mitteilung. Quassinoide Bitterstoffe II. Partialsynthetischer Zugang zu Quassin: Überführung von Testosteron in eine Schlüsselverbindung mit angulärer 8β-Methylgruppe
Johannes Pfenninger, Walter Graf
Structure      13C NMR   碳谱模拟图

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28 .     tuberostemonine C
C22H33NO4     相似度:54.1%
Journal of Chinese Pharmaceutical Sciences          1999          8          185-190
New Alkaloids from the Roots of Stemona japonica Miq.
Zou Changying; Fu Hongzheng; Lei Haimin; Li Jun and Lin Wenhan
Structure      13C NMR   碳谱模拟图

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29 .     N-oxy-tuberostemonine
C22H33NO5     相似度:54.1%
Journal of Chinese Pharmaceutical Sciences          1999          8          1-7
Three New Alkaloids from the Roots of Stemona tuberosa Lour
Lin Wenhan and Fu Hongzheng
Structure      13C NMR   碳谱模拟图

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30 .     (22S,24R)-[26,27-2H6]22-Hydroxy-24-methyl-3α,5-cyclo-5α-cholestan-6-one
C28H40D6O2     相似度:54.1%
Steroids          2002          67          1101-1108
Synthesis of hexadeuterated 23-dehydroxybrassinosteroids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Andrey P. Antonchick, Olga V. Konstantinova, Bernd Schneider
Structure      13C NMR   碳谱模拟图

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31 .     19-Hydroxy-6β-methoxy-3α,5-cyclo-5α-pregnan-20-one
C22H34O3     相似度:54.1%
Steroids          2004          69          161-171
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