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paopaoxiaozhu: ½ð±Ò+20, ¡ïÓаïÖú 2012-07-17 20:43:22
1 .     (S)-6-((1R,3aR,7aR,E)-4-(bromomethylene)-7a-methyloctahydro-1H-inden-1-yl)-2-methylheptane-2-ol
C19H33BrO     ÏàËÆ¶È:64.7%
Heterocycles          2010          81          381-394
Synthesis of 20-Epi-eldecalcitol [20-Epi-1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3: 20-Epi-ED-71]
Madoka Yoshino, Kohei Eto, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Yoshiyuki Ono, Hitoshi Saito, and Noboru Kubodera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 2
    ÏàËÆ¶È:64.7%
Phytochemistry          1985          24          977-979
Diterpenoid hydrocarbons in the sea grass Amphibolis antartica
Robert W. Dunlop
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     20(S)-20,21-Aziridinylpregn-4-en-3-one
C21H31NO     ÏàËÆ¶È:61.9%
Bioorganic & Medicinal Chemistry          1996          4          1447-1453
20-Amino and 20,21-aziridinyl pregnene steroids: Development of potent inhibitors of 17¦Á-hydroxylase/C17,20-lyase (P450 17)
Vincent C.O. Njar, Markus Hector, Rolf W. Hartmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     20(R)-20,21-Aziridinylpregn-4-en-3-one
C21H31NO     ÏàËÆ¶È:61.9%
Bioorganic & Medicinal Chemistry          1996          4          1447-1453
20-Amino and 20,21-aziridinyl pregnene steroids: Development of potent inhibitors of 17¦Á-hydroxylase/C17,20-lyase (P450 17)
Vincent C.O. Njar, Markus Hector, Rolf W. Hartmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4-thia-5¦Á-androstanone
C18H26OS     ÏàËÆ¶È:61.1%
Tetrahedron          2005          61          3691-3696
Shielding effect of thioether C¨CS bond from proton chemical shifts of 4-thia-5¦Á- and 4-thia-5¦Â-androstane-17-ones
Hajime Iwamoto, Takefumi Kawatani, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4-Aza-pregnane-3,20-dione-20-oxime
    ÏàËÆ¶È:60%
Molecules          2012          17          355-368
Synthesis and 5¦Á-Reductase Inhibitory Activity of C21 Steroids Having 1,4-diene or 4,6-diene 20-ones and 4-Azasteroid 20-Oximes
Sujeong Kim, Yong-ung Kim and Eunsook Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     17¦Â-hydroxy-4-androsteno[3,2-c]pyrazole
    ÏàËÆ¶È:60%
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   Ì¼Æ×Ä£Äâͼ
8 .     20¦Á-acetoxypregn-4-en-3-one
    ÏàËÆ¶È:59.0%
Steroids          1998          63          484-495
Microbial hydroxylation of acetylaminosteroids
HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     grenadamide
C21H33NO     ÏàËÆ¶È:58.8%
Journal of Natural Products          1998          61          681-684
Grenadadiene and Grenadamide, Cyclopropyl-Containing Fatty Acid Metabolites from the Marine Cyanobacterium Lyngbya majuscula
Namthip Sitachitta and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (2R,3R)-2-Hydroxy-3-(hydroxymethyl)-3,5-dimethyl-N-(3-oxo-3-(pentylamino)propyl)hexanamide
C17H34N2O4     ÏàËÆ¶È:58.8%
Bioorganic & Medicinal Chemistry          2011          19          2696-2706
Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity
T. Olukayode Akinnusi, Kenward Vong, Karine Auclair
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     15,16-trinorlabda-8(17),11-(E)dien-3-carboxylic acid
C17H26O2     ÏàËÆ¶È:58.8%
Natural Product Research and Development          2009          21          10-12
Norditerpenoids from Hedychium villosum
ZHAO Qing; HAO Xiao-jiang; ZOU Cheng; ZHANG Rong-ping; HU Jian-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (-)-thujopsene
    ÏàËÆ¶È:58.8%
Russian Journal of Organic Chemistry          2001          37          362-374
Acid-Catalyzed Rearrangements of (-)-Thujopsene
O. I. Yarovaya, M. P. Polovinka, D. V. Korchagina, Yu. V. Gatilov and I. Yu. Bagryanskaya, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     17¦Â-Hydroxyandrost-4-ene-3-one
    ÏàËÆ¶È:57.8%
Steroids          2006          71          979-983
Microbial transformation of androst-4-ene-3,17-dione by Beauveria bassiana
Zhigang Xiong, Qi Wei, Hanmei Chen, Shouwen Chen, Wenjin Xu, Guofu Qiu, Shucai Liang, Xianming Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     testosterone
    ÏàËÆ¶È:57.8%
Natural Product Research          2008          22          1498-1509
Microbial transformation of testosterone by Rhizopus stolonifer and Fusarium lini
Amal Al-Aboudi; Mohammad Yasin Mohammad; S. Ghulam Musharraf; M. Iqbal Choudhary; Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2R,3R)-2-Hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-3-(pentylamino)propyl)nonanamide
C19H38N2O4     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2011          19          2696-2706
Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity
T. Olukayode Akinnusi, Kenward Vong, Karine Auclair
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     testosterone
    ÏàËÆ¶È:57.8%
Steroids          1995          60          337-352
Microbial transformation of steroids: Contribution to 14¦Á-hydroxylations
Shang-hui Hu, Gilles Genain, Robert Azerad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     testosterone
    ÏàËÆ¶È:57.8%
Steroids          1992          57          122-134
Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17¦Á-hexanoic derivatives of 5¦Á-dihydrotestosterone and testosterone
Elisabeth Mappus, M¨¦lanie Renaud, Marc Rolland de Ravel, Catherine Grenot, Claude Y. Cuilleron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     testosterone
    ÏàËÆ¶È:57.8%
Steroids          1984          43          545-558
Metabolism of progesterone and testosterone by a Bacillus sp.
Shashi B. Mahato, Sukdeb Banerjee, Niranjan P. Sahu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound 2
    ÏàËÆ¶È:57.8%
Journal of the Chemical Society, Perkin Transactions 1          1975                   1956-1958
13 C nuclear magnetic resonance spectra of some steroidal unsaturated ketones
James R. Hanson and Michael Siverns
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     testosterone
    ÏàËÆ¶È:57.8%
Zeitschrift f¨¹r Naturforschung C          2010          65          688-692
Biotransformation of Some Steroids by Aspergillus wentii
K. Yildirim, I. Kupcu, and F. Gulsan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     17¦Â-Hydroxyandrost-4-en-3-one testosterone
C19H28O2     ÏàËÆ¶È:57.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     20-Hydroxyimino-4-pregnene-3,20-dione
    ÏàËÆ¶È:57.1%
Molecules          2009          14          4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     cholest-4-ene-3,6-diol
C27H46O2     ÏàËÆ¶È:57.1%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     17¦Â-hydroxy-4-androsteno[3,2-c]-[1']-5'-methylthiopyrazole
    ÏàËÆ¶È:57.1%
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   Ì¼Æ×Ä£Äâͼ
25 .     17¦Â-acetylaminoandrost-4-en-3-one
    ÏàËÆ¶È:57.1%
Steroids          1998          63          484-495
Microbial hydroxylation of acetylaminosteroids
HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     17¦Á-Pregna-4,20-dien-3-one
C21H30O     ÏàËÆ¶È:57.1%
Journal of the Chinese Chemical Society          2004          51          205-208
Pregnane-Based Steroids from a Formosan Gorgonian Subergorgia mollis
Shwu-Li Wu, Guey-Horng Wang Chang-Feng Dai and Jyh-Horng Sheu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     5¦Á-Pregnane
C21H36     ÏàËÆ¶È:57.1%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (20S)-De-A,B-cholestane-8¦Â,25-diol
C18H32O     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2000          8          123-134
Efficient synthesis and biological evaluation of all a-ring diastereomers of 1¦Á,25-dihydroxyvitamin D3 and its 20-epimer
Toshie Fujishima, Katsuhiro Konno, Kimie Nakagawa, Mayuko Kurobe, Toshio Okano, Hiroaki Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     5¦Á-Androstan-16-one
C19H30O     ÏàËÆ¶È:55.5%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     5¦Á-Androstan-17-one
C19H30O     ÏàËÆ¶È:55.5%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     4'-Dehydro-androst-4-eno[3,4-e]piperazin-6,17-dione
    ÏàËÆ¶È:55%
Steroids          2008          73          539-542
Microwave promoted one-pot synthesis of novel A-ring fused steroidal dehydropiperazines
Moyurima Borthakur, Madan G. Barthakur, Romesh C. Boruah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     17¦Â-hydroxy-4-androsteno[2,3-d]isoxazole
    ÏàËÆ¶È:55%
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   Ì¼Æ×Ä£Äâͼ
33 .     Compound 14
    ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry Letters          2006          16          1656-1659
Synthesis and biological activity of (+)-hedychilactone A and its analogs from (+)-sclareolide
Sangtae Oh, In Howa Jeong, Woon-Seob Shin, Qian Wang, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     (E)-(20S)-De-A,B-8-(bromomethylene)cholestan-25-ol
C19H33BrO     ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry          2000          8          123-134
Efficient synthesis and biological evaluation of all a-ring diastereomers of 1¦Á,25-dihydroxyvitamin D3 and its 20-epimer
Toshie Fujishima, Katsuhiro Konno, Kimie Nakagawa, Mayuko Kurobe, Toshio Okano, Hiroaki Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     3¦Â-hydroxy-cholest-5-en-19-oic acid sulfate sodium salt
    ÏàËÆ¶È:55%
Experientia          1983          39          759-761
Biologically-active sterol sulfates from the marine spongeToxadocia zumi
T. Nakatsu, R. P. Walker, J. E. Thompson and D. J. Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     7¦Á-hydroxycholestanone
C27H46O2     ÏàËÆ¶È:54.5%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     cholest-5-ene-3,7-dione
C27H42O2     ÏàËÆ¶È:54.5%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 15
    ÏàËÆ¶È:52.9%
Phytochemistry          2005          66          249-260
Sesquiterpenes from Cupressus macrocarpa foliage
Laurence G. Cool
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     coronadiene
C17H26O2     ÏàËÆ¶È:52.9%
Chemical & Pharmaceutical Bulletin          2008          56(12)          1704-1709
Medicinal Flowers. XXIV.1) Chemical Structures and Hepatoprotective Effects of Constituents from Flowers of Hedychium coronarium
Seikou NAKAMURA,Yoshie OKAZAKI,Kiyofumi NINOMIYA,b Toshio MORIKAWA,Hisashi MATSUDA,and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     plagio-4,7-peroxide
    ÏàËÆ¶È:52.9%
Phytochemistry          2005          66          599-609
Sesquiterpene constituents from the essential oil of the liverwort Plagiochila asplenioides
Adewale Martins Adio, Wilfried A. K?nig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     (R)-10-methyl-6-undecanolide
    ÏàËÆ¶È:52.9%
Journal of Natural Products          2004          67          395-401
Novel Caprolactones from a Marine Streptomycete
Katja Stritzke, Stefan Schulz, Hartmut Laatsch, Elisabeth Helmke, and Winfried Beil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     Pivaloyl-(S)-tert-leucyl-(2e,4S)-N-methyl-4-amino-2,5-dimethylhex-2-enoic acid
C20H36N2O4     ÏàËÆ¶È:52.9%
Journal of Natural Products          2003          66          183-199
Synthesis and Antimitotic/Cytotoxic Activity of Hemiasterlin Analogues
James A. Nieman, John E. Coleman, Debra J. Wallace, Edward Piers, Lynette Y. Lim, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     neostenine-diol
    ÏàËÆ¶È:52.9%
Planta Medica          2003          69          914-920
Antitussive Activity of Stemona Alkaloids from Stemona tuberosa
Hoi-Sing Chung,Po-Ming Hon,Ge Lin,Paul Pui-Hay But,Hui Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     ambreinolide
    ÏàËÆ¶È:52.9%
Helvetica Chimica Acta          1980          63          1932-1946
Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances
G¨¹nther Ohloff, Christian Vial, Hans Richard Wolf, Kurt Job, Elise J¨¦gou, Judith Polonsky, Edgar Lederer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     isoambreinolide
    ÏàËÆ¶È:52.9%
Helvetica Chimica Acta          1980          63          1932-1946
Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances
G¨¹nther Ohloff, Christian Vial, Hans Richard Wolf, Kurt Job, Elise J¨¦gou, Judith Polonsky, Edgar Lederer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     Endo ethyl 4,5-dibromobicyclo[6.1.0]nonane-9-carboxylate
    ÏàËÆ¶È:52.9%
Molecules          2007          12          2427-2433
A Simple and Efficient Approach to the Synthesis of Endo and Exo Bicyclo[6.1.0]nona-3, 5-diene-9-carboxaldehyde
Mehdi Ghandi and Gholamreza Mashayekhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     d5-androsterone
C19H25D5O2     ÏàËÆ¶È:52.9%
Steroids          2003          68          85-96
A facile and high yielding synthesis of 2,2,3,4,4-d5-androsterone-¦Â--glucuronide¡ªan internal standard in dope analysis
Peter G?rtner, Clemens Novak, Christian Einzinger, Wolfgang Felzmann, Max Knollm¨¹ller, G¨¹nter Gmeiner, Wilhelm Sch?nzer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     (13S,17R)-17-Hydroxy-13,14-seco-androst-4-en-3-one
C19H30O2     ÏàËÆ¶È:52.9%
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   Ì¼Æ×Ä£Äâͼ
49 .     6¦Â-Hydroxy-5¦Â-methyl-19-norcholest-9(10)-en-3¦Â-ylacetate
C29H48O3     ÏàËÆ¶È:52.9%
Steroids          2008          73          549-561
Bismuth(III) salt-catalyzed Westphalen and ¡°backbone¡± rearrangements of 5¦Â,6¦Â-epoxysteroids: Synthesis and structural elucidation of new olefinic 19-nor and 18,19-dinorsteroids
Rui M.A. Pinto, Jorge A.R. Salvador, Christophe Le Roux, Rui A. Carvalho, Manuela Ramos Silva, Ana Matos Beja, Jos¨¦ A. Paix?o
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     12-hydroxy-¦Â-caryophyllene acetate
    ÏàËÆ¶È:52.9%
Natural Product Research          1997          11          25-30
¦Â-Caryophyllene Derivatives from the Wild Cottons
Howard J. Williams; Guillermo Moyna; S. Bradleigh Vinson; A. Ian Scott; Alois A. Bell; Robert D. Stipanovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     6¦Á-methoxy-pinguis-5(10)-en-11,6-olide
16H24O3     ÏàËÆ¶È:52.9%
Phytochemistry          1998          49          1079-1083
Pinguisane sesquiterpenes from the liverwort porella Navicularis,
Michael Bungert, Jens Gabler, Klaus-Peter Adam, Josef Zapp, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     3¦Â,5¦Â-dihydroxycostic acid
C15H22O4     ÏàËÆ¶È:52.9%
Phytochemistry          1997          44          897-900
Sesquiterpenes from Tessaria absinthioides
Marcela B. Kurina Sanz, Osvaldo J. Donadel, Pedro C. Rossomando, Carlos E. Tonn, Eduardo Guerreiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     acetylginsenol
    ÏàËÆ¶È:52.9%
Journal of Natural Products          1994          Vol 57          738
Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene
Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     drimenol
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Phytochemistry          1994          35          975-977
Drimendiol, a sesquiterpene from Drymis winterii
Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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