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12.27,14.72,20.53,21.62,21.99,22.41,24.03,24.97,26.05,29.23,29.68,31.16,31.36,31.87,34.91,37.30,39.41,44.03,55.38,56.43,68.36,69.98,77.20,78.98,82.72,107.65,114.39
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̸ÅÐÌÕ: ½ð±Ò+10, ¡ïÓаïÖú, лл 2013-10-01 22:37:48
1 .     compound 6b
    ÏàËÆ¶È:67.8%
Steroids          1984          43          639-649
24¦Î-Methyl-5¦Á-cholestane-3¦Â,5,6¦Â.22r.24-pentol 6-acetate: New polyhydroxylated sterol from the soft coral asterospicularia randalli.
Mohamad B. Ksebati, Francis J. Schmitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     5¦Á-Cholestane-3¦Â,5,6¦Â-triol 3,6-diacetate
C31H52O5     ÏàËÆ¶È:67.8%
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

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3 .     cholest-5-en-1¦Á,3¦Â,4¦Á-triol
C27H46O3     ÏàËÆ¶È:66.6%
Steroids          2013          78          38-43
Cytotoxic cholestane-type and ergostane-type steroids from the aerial parts of Euphorbia altotibetic
Bei-Bei Zhang, Xue-Lian Han, Qian Jiang, Zhi-Xin Liao, Heng-Shan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 6f
    ÏàËÆ¶È:66.6%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     4¦Á-¼×»ù-Âó½ÇçÞ-24-Ï©-3¦Â-´¼
    ÏàËÆ¶È:65.5%
Chinese Journal of Medicinal Chemistry          2007          17          95-100
Chemical constituents from soft coral Sinularia dissecta in south China sea
JIN Peng-fei, LIN Wen-han, DENG Zhi-wei, PEI Yue-hu, SUN Chun-hua, Hu Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     compound 9
    ÏàËÆ¶È:65.5%
Australian Journal of Chemistry          1975          28          1017-1021
Carbon-13 N.M.R. spectra of 6¦Â-Substituted-5¦Á-cholestane-3¦Â,5-diols: ¦Ã- and ¦Ä-effects
JW Blunt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     muriflasteroid B
C28H48O3     ÏàËÆ¶È:64.2%
Steroids          2013          78          108-114
3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function
Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     5¦Á-Cholestane-3¦Â,5,6¦Á-triol 3-acetate
C29H50O4     ÏàËÆ¶È:64.2%
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

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9 .     5¦Á-Cholestane-3¦Â,5,6¦Á-triol 3,6-diacetate
C31H52O5     ÏàËÆ¶È:64.2%
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

--------------------------------------------------------------------------------




10 .     6¦Â-Fluoro-5¦Á-cholastane-3¦Â,5-diol 3-acetate
C29H49FO3     ÏàËÆ¶È:64.2%
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

--------------------------------------------------------------------------------




11 .     compound 3
    ÏàËÆ¶È:64.2%
Australian Journal of Chemistry          1975          28          1017-1021
Carbon-13 N.M.R. spectra of 6¦Â-Substituted-5¦Á-cholestane-3¦Â,5-diols: ¦Ã- and ¦Ä-effects
JW Blunt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (22E)-24-ethyl-4¦Á-methyl-5¦Á-cholest-22-en-3¦Â-ol
    ÏàËÆ¶È:63.3%
Fitoterapia          2005          76          433-438
A new dihydroxysterol from the marine phytoplankton Diacronema sp.
Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 3
    ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1985          33          67-73
Studies on the Constituents of Solanum Plants. V. The Constituents of S. lyratum THUNB. II
KOTARO MURAKAMI,HISATAKA EZIMA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSURO FUJITA,AKIHIKO SATO,YOKO NAGAYAMA and TOSHIHIRO NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 4
    ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1985          33          67-73
Studies on the Constituents of Solanum Plants. V. The Constituents of S. lyratum THUNB. II
KOTARO MURAKAMI,HISATAKA EZIMA,YOSHIHISA TAKAISHI,YOSHIO TAKEDA,TETSURO FUJITA,AKIHIKO SATO,YOKO NAGAYAMA and TOSHIHIRO NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (20R,22S)-2¦Á,3¦Á,20,22-Tetrahydroxy-5¦Á-cholestan-6-one
C27H46O5     ÏàËÆ¶È:62.9%
Steroids          2004          69          483-493
Stereoselective synthesis of (22R)- and (22S)-castasterone/ponasterone A hybrid compounds and evaluation of their molting hormone activity
Bunta Watanabe, Yoshiaki Nakagawa, Takehiko Ogura, Hisashi Miyagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     1-((3R,10S,13S,17S)-Hexadecahydro-3-hydroxy-3-(methoxymethyl)-10,13-dimethyl-1H-cyclopenta[a]phenanthren-17-yl)-2-(pyrrolidin-1-yl)ethanone
C27H43NO3     ÏàËÆ¶È:62.9%
Steroids          2006          71          942-948
The mechanism investigation in substitution of 21-bromo-3¦Á-hydroxyl-3¦Â-methoxymethyl-5¦Á-pregnan-20-one with nucleophiles
Chun-Yen Chen, Fung Fuh Wong, Yueh-Hsien Lee, Shan-Yen Chou, Jiann-Jyh Huang, Mou-Yung Yeh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     4¦Â,5¦Â-Epoxycholestan-3¦Â-ol
    ÏàËÆ¶È:62.9%
Steroids          2007          72          643-652
Atypical regioselective biohydrolysis on steroidal oxiranes by Aspergillus niger whole cells: Some stereochemical features
Fabricio R. Bisogno, Alejandro A. Orden, Celeste Aguirre Pranzoni, Diego A. Cifuente, Oscar S. Giordano, Marcela Kurina Sanz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 16
C27H44O2     ÏàËÆ¶È:62.9%
Steroids          2007          72          643-652
Atypical regioselective biohydrolysis on steroidal oxiranes by Aspergillus niger whole cells: Some stereochemical features
Fabricio R. Bisogno, Alejandro A. Orden, Celeste Aguirre Pranzoni, Diego A. Cifuente, Oscar S. Giordano, Marcela Kurina Sanz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (22R)-2¦Á,3¦Á,5¦Á-Trihydroxy-furostan-6-one
C27H43O5     ÏàËÆ¶È:62.9%
Steroids          2007          72          955-959
Synthesis and biological activity of furostanic analogues of brassinosteroids bearing the 5¦Á-hydroxy-6-oxo moiety
Margarita Romero-Avila, Guadalupe de Dios-Bravo, J¨®se M. Mendez-Stivalet, Rogelio Rodr¨ªguez-Sotres, Martin A. Iglesias-Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     3-Oxa-7¦Á,12¦Á,24-trimethoxy-5¦Â-cholane
C26H46O4     ÏàËÆ¶È:62.9%
Steroids          2010          75          701-709
First synthesis of thia steroids from cholic acid
Malika Ibrahim-Ouali, Luc Rocheblave
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     compound 7
C27H42O8     ÏàËÆ¶È:62.9%
Heterocycles          2003          59          645-659
Structures of Two New Highly Oxygenated Labdane-Type Diterpenoids and a New Cadinane-Type Sesquiterpenoid Possessing a Cyclic Ether Linkage from the Liverwort Ptychanthus striatus
Toshihiro Hashimoto, Shigeru Takaoka, Masami Tanaka, and Yoshinori Asakawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     petilidine
    ÏàËÆ¶È:62.9%
Chinese Traditional and Herbal Drugs          2009          40          15-17
Alkaloid constituents of Fritillaria cirrhosa
CAO Xin-wei; ZHANG Meng; LI Jun; XIAO Pei-gen; CHEN Si-bao; CHEN Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (24S)-3¦Â-hydroxy-5¦Á-stigmastan-6-one
C29H50O2     ÏàËÆ¶È:62.9%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     16¦Â-(4-Hexyl-1,2,3-triazol-1-yl)-17-hydroxy-5-androstane
C27H45N3O     ÏàËÆ¶È:62.9%
Steroids          2012          77          738-744
Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes
Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     2¦Â-(n-heptylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C26H47NO2     ÏàËÆ¶È:62.9%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     terminamine F
C27H43NO2     ÏàËÆ¶È:62.9%
Journal of Natural Products          2012          75          1305-1311
Alkaloids from Pachysandra terminalis Inhibit Breast Cancer Invasion and Have Potential for Development As Antimetastasis Therapeutic Agents
Hui-Yuan Zhai, Chuan Zhao, Ning Zhang, Mei-Na Jin, Sheng-An Tang, Nan Qin, De-Xin Kong, and Hong-Quan Duan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     compound 43
C30H50O4     ÏàËÆ¶È:62.9%
Journal of the American Chemical Society          2010          132          5300-5308
Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone
Matthew A. Boone, Rongbiao Tong, Frank E. McDonald, Sheri Lense, Rui Cao and Kenneth I. Hardcastle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     cholest-5-en-2¦Â,4¦Â-diol
C27H46O2     ÏàËÆ¶È:62.9%
Steroids          2013          78          38-43
Cytotoxic cholestane-type and ergostane-type steroids from the aerial parts of Euphorbia altotibetic
Bei-Bei Zhang, Xue-Lian Han, Qian Jiang, Zhi-Xin Liao, Heng-Shan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




29 .     cholest-5-en-1¦Â,4¦Â-diol
C27H46O2     ÏàËÆ¶È:62.9%
Steroids          2013          78          38-43
Cytotoxic cholestane-type and ergostane-type steroids from the aerial parts of Euphorbia altotibetic
Bei-Bei Zhang, Xue-Lian Han, Qian Jiang, Zhi-Xin Liao, Heng-Shan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     ¡÷20-cholesterol
C32H64O2     ÏàËÆ¶È:62.9%
Indian Journal of Chemistry          1996          35B          627-629
Chemical constituents of Zoanthus species CDR-83:Cholesta-5,20-dien-3¦Â-ol,a rare sterol
U V Babu, S P S Bhandari & H S Garg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     compound 7
    ÏàËÆ¶È:62.9%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     5¦Á-Cholestan-3¦Â-ol
C27H48O     ÏàËÆ¶È:62.9%
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

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33 .     calysterol
    ÏàËÆ¶È:62.9%
Journal of the American Chemical Society          1988          110          8124-8128
Sterols in marine invertebrates. 60. Isolation and structure elucidation of four new steroidal cyclopropenes from the sponge Calyx podatypa
George A. Doss, Carl. Djerassi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     compound 6g
    ÏàËÆ¶È:62.9%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




35 .     compound 6h
    ÏàËÆ¶È:62.9%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




36 .     4¦Á-Hydroxy
    ÏàËÆ¶È:62.9%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




37 .     stereonsteroid C
C29H46O7     ÏàËÆ¶È:62.0%
Journal of Natural Products          2006          69(1)          103-106
Cytotoxic Pregnane Steroids from the Formosan Soft Coral Stereonephthya crystalliana
Shang-Kwei Wang, Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     3¦Â-Acetoxy-5-hydroxy-5¦Á-cholestan-6-one
    ÏàËÆ¶È:62.0%
Steroids          2012          77          461-466
Synthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5a-hydroxy-6-oxo moiety and cholestane side chain
Anielka Rosado-Ab¨®n, Guadalupe de Dios-Bravo ,Rogelio Rodr¨ªguez-Sotres ,Mart¨ªn A. Iglesias-Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     nebrosteroid P
C29H50O4     ÏàËÆ¶È:62.0%
Marine Drugs          2012          10          1288-1296
New 19-Oxygenated Steroids from the Soft Coral Nephthea chabrolii
Shang-Kwei Wang, Shyh-Yueh Puu and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     (24R)-[26-2H3]-6¦Â-methoxy-24-methyl-3¦Á,5-cyclo-5¦Á-cholestane
    ÏàËÆ¶È:62.0%
Chemistry of Natural Compounds          2012          48          606-609
Synthesis of [26-2H3]-campesterin and [26-2H3]-campestanol, deuterated analogs of biosynthetic precursors of 28C-brassinosteroids
V. A. Khripach, V. N. Zhabinskii, Yu. V. Ermolovich and O. V. Gulyakevich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     3'¦Á-chloro-2'-oxo-tetrahydrofuran[4',5':2,3](2R,3S,3'R)-2¦Â-methyl-5¦Á-cholestane
C30H49ClO2     ÏàËÆ¶È:62.0%
Tetrahedron          2012          68          9061-9067
Stereoelectronic and steric effect in the Baeyer¨CVilliger rearrangement of steroidal ¦Á-chlorocyclobutanones
Zdzisław Paryzek, Hanna Koenig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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