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11.8,16.6,17.6,18.8,19.3,21.0,24.2,28.2,28.3,28.4,28.5,31.3,31.8,35.9,36.2,
36.4,37.2,42.0,42.3,50.0,55.8,56.7,71.5,89.0, 116.0,121.6,137.4,140.7

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¶¹¸ç: ½ð±Ò+1, лл²ÎÓë½»Á÷ 2012-06-06 13:19:50
myvalerie: ½ð±Ò+10, ¡ïÓаïÖú, ¶àлÁË£¡ 2012-06-06 15:55:10
1 .     24-hydroperoxy-24-vinylcholesterol
    ÏàËÆ¶È:89.6%
Natural Product Research          2012          26          774-777
Sterols from Sargassum oligocystum, a brown algae from the Persian Gulf, and their bioactivity
Parisa Permeh, Soodabeh Saeidnia, Ali Mashinchian-Moradi and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     24-hydroxyperoxy-24-vinylcholesterol
C29H46O2     ÏàËÆ¶È:89.6%
Journal of the Chinese Chemical Society          1991          38          501-503
Isolation of 24-Hydroperoxy-24-vinylcholesterol and Fucosterol from the Brown Alga Turbinaria conoldes
ÔSÖ¾ºê(Jyh-Horng Sheu);Ëαüâx(Ping-Jyun Sung)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     cystosphaerol
    ÏàËÆ¶È:89.2%
Journal of Natural Products          2004          67          1295-1302
Chemical Investigation of Predator-Deterred Macroalgae from the Antarctic Peninsula
Sridevi Ankisetty, Santhisree Nandiraju, Hla Win, Young Chul Park, Charles D. Amsler, James B. McClintock, Jill A. Baker, Thushara K. Diyabalanage, Albert Pasaribu, Maya P. Singh, William M. Maiese, Rosa D. Walsh, Michael J. Zaworotko, and Bill J. Baker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     24-hydroperoxy-24-vinylcholesterol
    ÏàËÆ¶È:86.2%
Journal of the Chinese Chemical Society          2001          48          821-826
Ceramides from the Taiwan Red Alga Ceratodictyon spongiosum and Symbiotic Sponge Sigmadocia symbiotica
Jir-Mehng Lo, Wei-Lung Wang,Young-Meng Chiang and Chiu-Ming Chen*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     saringosterol
C29H48O2     ÏàËÆ¶È:86.2%
Zeitschrift f¨¹r Naturforschung C          2003          58          333-336
The Structural Determination of a New Steroidal Metabolite from the Brown Alga Sargassum asperifolium
S.-E. N. Ayyad, S. Z. A. Sowellim, M. S. El-Hosini, and A. Abo-Atia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Isofucosterol
C29H48O     ÏàËÆ¶È:82.1%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          335-338
STUDIES ON THE CONSTITUENTS OF THE GREEN ALGA Ulva lactuca
El Sayed H. El Ashry, Atta-ur-Rahman, M. Iqbal Choudhary, Sherif H. Kandil, Ahmed El Nemr, Tahsin Gulzar, and Aida H. Shobier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Alkesterol B
C28H44O2     ÏàËÆ¶È:82.1%
Journal of Asian Natural products Research          2010          12          752-759
C28 sterols with a cyclopentane ring at C-22 and 26 from cape gooseberry (berries of Physalis pubeacens L.)
Qiong-Ming Xu; Yan-Li Liu; Yu-Lin Feng; Xiao-Ran Li; Shi-Lin Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (24¦Î)-24-Ethyl-24-methylcholesterol
    ÏàËÆ¶È:80%
Steroids          2004          69          93-100
Ophirasterol, a new C31 sterol from the marine sponge Topsentia ophiraphidites
Gladys J. Calder¨®n, Leonardo Castellanos, Carmenza Duque, Shizue Echigo, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     isofucosterol
    ÏàËÆ¶È:79.3%
Phytochemistry          2004          65          2463-2470
Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae)
Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (24S)-stigmast-5-ene-3¦Â,24-diol
C29H50O2     ÏàËÆ¶È:79.3%
Chemical & Pharmaceutical Bulletin          1998          46          1408-1411
New Sterols and Triterpenoids of Ficus pumila Fruit
Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     pro-R-methyl-13C-labeled isofucosterol
    ÏàËÆ¶È:79.3%
Phytochemistry          2000          54          381-385
Stereochemical fate of C-26 and C-27 during the conversion of isofucosterol to sitosterol and of 24-methylenecholesterol to campesterol and dihydrobrassicasterol in Oryza sativa cell cultures
Kozue Nasu, Kyoko Takahashi, Masuo Morisaki, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     ÂíβÔåçÞ´¼
    ÏàËÆ¶È:79.3%
Chinese Journal of Marine Drugs          2002          21(1)          1-4
Sterol con stituents from marine brown alga ishige okamurai
TANG Hai-feng, YI Yang-hua, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Saringosterol
C29H48O2     ÏàËÆ¶È:79.3%
Chemistry of Natural Compounds          2012          48          158-160
STEROIDS AND TRITERPENOIDS FROM THE BROWN ALGA Kjellmaniella crassifolia
Ze-Hong Wu,Tao liu,Chen-Xi Gu,Chang-Lun Shao,Jing Zhou,and Chang-Yun Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (24S)5,28-stigmastadien-3¦Â,24-diol
    ÏàËÆ¶È:79.3%
Chinese Traditional and Herbal Drugs          2008          39          657-661
Chemical constituents from brown alga Sargassum fusiforme
WANG Wei; LI Hong-yan; WANG Yan-yan; XIA Xue; OKADA Yoshihto; OKUYAMA Toru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     saringosterol
C29H48O2     ÏàËÆ¶È:79.3%
Chinese Journal of Natural Medicines          2007          5          186-189
Chemical Constituents from Physalis alkekengi and Structural Revision of Physalin G
CHEN Rong; LIANG Jing-Yu; YANG Yang; LIU Rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     saringosterol
    ÏàËÆ¶È:79.3%
Chinese Pharmaceutical Journal          2002          37          262-265
Studies on the bioactive steroid constituents from Sargassum carpophyllum
TANG Hai-feng, YI Yang-hua, YAO Xin-sheng, ZHOU Da-zheng, LÜ Tai-sheng, JIANG Yong-pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ¶¹çÞ-5,24 (28) ¶þÏ©-3¦Â-´¼
    ÏàËÆ¶È:79.3%
Journal of Shenyang Pharmaceutical University          2006          23          358-360
Studies on the chemical constituents of Ulva lactuca L.
SUN Yi, HOU Bai-ling, YANG Ying, PEI Yue-Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     [(13)C2H3]isofucosterol
    ÏàËÆ¶È:79.3%
Journal of the Chemical Society, Perkin Transactions 1          1990                   105-109
Biosynthesis of isofucosterol from [2-13C2H3]acetate and [1,2-13C2]acetate in tissue cultures of Physalis peruviana−the stereochemistry of the hydride shift from C-24 to C-25
Shujiro Seo, Atsuko Uomori, Yohko Yoshimura, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi, Ushio Sankawa and Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     20-epi-verazine
C28H15N     ÏàËÆ¶È:78.5%
Journal of Natural Products          1998          61          1202-1208
DNA-Damaging Steroidal Alkaloids from Eclipta alba from the Suriname Rainforest1
Maged S. Abdel-Kader, Brian D. Bahler, Stan Malone, Marga C. M. Werkhoven, Frits van Troon, David.Jan H. Wisse, Isia Bursuker, Kim M. Neddermann, Stephen W. Mamber, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     physalindicanol B
C28H46O2     ÏàËÆ¶È:78.5%
Planta Medica          1987          53          55-57
Physalindicanols, New Biogenetic Precursors of C28-Steroidal Lactones from Physalis minima var. indica
Subhash C. Sinha, Abid Au, Anjana Bagchi, Mahendra Sahai and Anil B. Ray
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     cholesterol
    ÏàËÆ¶È:78.5%
Phytochemistry          1996          42          1141-1143
Somalenone, A C26 sterol from the marine red alga Melanothamnus somalensis
Viqar Uddin Ahmad, Abdul Hayee Memon, Mohammad Shaiq Ali, Shaista Perveen, Mustafa Shameel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (24S)-24¦Á-¼×»ùµ¨çÞ-5-Ï©-3¦Â,25-¶þ´¼((24S)-24¦Á-methylcholest-5-en-3¦Â,25-diol)
C28H48O2     ÏàËÆ¶È:78.5%
Chinese Journal of Marine Drugs          2002          21(1)          5-7,57
Chemical studies on the soft coral lobophytum j aeckel Tix. -Dur.
WANG Ming-yan, ZENG Long-mei, SU Jing-yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     25-hydroxycholestero
    ÏàËÆ¶È:78.5%
Steroids          1994          59          310-317
Inhibitors of sterol synthesis. Effects of fluorine substitution at carbon atom 25 of cholesterol on its spectral and chromatographic properties and on 3-hydroxy-3-methylglutaryl coenzyme a reductase activity in CHO-K1 cells
William K. Wilson, Shankar Swaminathan, Frederick D. Pinkerton, Nicolas Gerst, George J. Schroepfer Jr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Alkesterol A
C28H44O2     ÏàËÆ¶È:78.5%
Journal of Asian Natural products Research          2010          12          752-759
C28 sterols with a cyclopentane ring at C-22 and 26 from cape gooseberry (berries of Physalis pubeacens L.)
Qiong-Ming Xu; Yan-Li Liu; Yu-Lin Feng; Xiao-Ran Li; Shi-Lin Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     stigmasta-5,28¦Â-diene-3¦Â,14-diol
C29H48O2     ÏàËÆ¶È:75.8%
Natural Product Research          1999          13          255-261
Chemical Constituents From Marine Organisms
Atta Ur Rahman; M. Shabbir; A. Majeed Khan; Safdar Hayat; Amber Nasreen; Shahid Malik; M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     stigmast-23-en-3-ol
C29H50O     ÏàËÆ¶È:75.8%
Natural Product Research          2006          20          1271-1276
Sterols isolated from Tubifex tubifex
Rosa Martha Perez Gutierrez; Ivan Cordova Reyes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     24-hydroxyl-24-vinyl-cholesterol
    ÏàËÆ¶È:75.8%
Chinese Journal of Natural Medicines          2010          8          326-329
Chemical Constituents from Grateloupia filicina
XU Yin-Feng; WANG Bin; SU Chuan-Ling; QU You-Le
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     verazine
    ÏàËÆ¶È:75%
Journal of Natural Products          1998          61          1202-1208
DNA-Damaging Steroidal Alkaloids from Eclipta alba from the Suriname Rainforest1
Maged S. Abdel-Kader, Brian D. Bahler, Stan Malone, Marga C. M. Werkhoven, Frits van Troon, David.Jan H. Wisse, Isia Bursuker, Kim M. Neddermann, Stephen W. Mamber, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     cholesta-5,25-diene-3¦Â,24¦Î-diol
    ÏàËÆ¶È:75%
Journal of Natural Products          1996          59          23-26
Cytotoxic Oxygenated Desmosterols of the Red Alga Galaxaura marginata
Jyh-Horng Sheu, Shiang-Yuh Huang, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     (20S)-verazine
    ÏàËÆ¶È:75%
Planta Medica          1992          58          449-453
Epimeric (20R,20S)-Verazine Isolated from Veratrum maackii: Two-Dimensional NMR Studies and Total Assignment of 1H- and 13C-Resonances
Xiuwen Han and heinz Ruegger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     cholesterol
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     compound 1a
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     (24S)-24-methylcholest-5-ene-3¦Â,25-diol
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1983          31          1848-1855
Marine Sterols. XI. Polyhydroxysterols of the Soft Coral Sarcophyton glaucum : Isolation and Synthesis of 5¦Á-Cholestane-1¦Â, 3¦Â, 5, 6¦Â-tetrol
MASARU KOBAYASHI,TAKAAKI HAYASHI,KOJI HAYASHI,MASATO TANABE,TAKASHI NAKAGAWA and HIROSHI MITSUHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     cholesterol
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     cholesterol
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          1999          35          672-645
I3C NMR SPECTRA OF STEROL DERIVATIVES,INTERMEDIATES IN THE SYNTHESIS OF ECDY- AND BRASSINOSTEROIDS
N. V. Kovganko, Zh. N. Kashkan,and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     (25R)-Cholest-5-ene-3¦Â,26-diol
    ÏàËÆ¶È:75%
Steroids          2002          67          1041-1044
Synthesis of (25R)-26-hydroxycholesterol
John R Williams, Deping Chai, Dominic Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     (25S)-26-hydroxycholesterol
C27H46O2     ÏàËÆ¶È:75%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     (25R)-3¦Â-Hydroxy-cholest-5-en-26-oic acid
C27H44O3     ÏàËÆ¶È:75%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]chol-5-en-24-carbonitrile
C31H53NOSi     ÏàËÆ¶È:75%
Steroids          2006          71          484-488
Synthesis of ent-25-hydroxycholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-25-Hydroxycholesterol
C27H46O2     ÏàËÆ¶È:75%
Steroids          2006          71          484-488
Synthesis of ent-25-hydroxycholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     cholesterol
    ÏàËÆ¶È:75%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černý, Miloš Bud¨§š¨ªnský, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     3¦Â ,25-dihydroxy-5-ene
C27H46O2     ÏàËÆ¶È:75%
Steroids          2009          74          81-87
A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane
Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     isofucosterol
    ÏàËÆ¶È:75%
Natural Product Research          1998          11          207-210
Metabolic Origin of c-26 and c-27 of Isofucosterol in Tissue Cultures of Catharanthus roseus
Yoshinori Fujimoto; Naoko Sato; Yasuyo Sekiyama; Michiko Ito; Takayuki Suzuki; Hiroki Hamada; Masuo Morisaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     24-¦Â-methylcholesterol
    ÏàËÆ¶È:75%
Journal of Natural Products          1981          Vol 44          7-13
Proof of Structure For 24¦Â-Methylcholesterol in the Alga Coccomyxa elongata by 1H- and 13C-nmr and Mass Spectroscopy
William R. Nes, John E. Zarembo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     fucosterol
    ÏàËÆ¶È:75%
Natural Product Sciences          2004          10          29-31
Determination of Fucosterol in the Marine Algae Pelvetia siliquosa by Gas Chromatography
Lee, Sang-Hyun; Lee, Yeon-Sil; Jung, Sang-Hoon; Lee, Hye-Seung; Kang, Sam-Sik; Shin, Kuk-Hyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     cholesterol
C27H46O     ÏàËÆ¶È:75%
Natural Product Sciences          2007          13          220-224
Antioxidant Activity of Cholesterol Derived from Silkworm Pupae
Heo, Jung-Eun; Ryu, Jae-Ha; Jeong, Hye-Kyoung; Chung, Wan-Tae; Ahn, Mi-Young
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     Cholesterol
    ÏàËÆ¶È:75%
Chemical Journal of Chinese Universities          2007          28          686-688
Isolation of New Polyhydroxylated Sterol from Soft Coral Sarcophyton crassocaule Mosre
ZHANG Cui-Xian, YAN Su-Jun, ZHANG Guang-Wen, SU Jing-Yu, ZENG Long-Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     cholest-5-en-3¦Â-ol
    ÏàËÆ¶È:75%
Chemical Journal of Chinese Universities          1996          17          249-251
Studies on the Chemical Constituent of Laurencia Karlae Collected from the South China Sea
ZHONG Yong-Li,SU Jing-Yu,ZENG Long-Me,YAN Su-Jun,LUO Bing-Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     µ¨çÞ´¼(eholesterol)
    ÏàËÆ¶È:75%
Chinese Journal of Marine Drugs          2010          29(6)          29-33
Study on the anticancer activities and chemical constituents of the Grateloupia filicina C.Ag.
LI Ya-qi, ZHANG Zhao-hui, PANG Jun-fang, WANG Shun-chun, CHEN Yi-lei, ZHOU Qiao-yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     Cholesterol
C27H46O     ÏàËÆ¶È:75%
Chinese Journal of Marine Drugs          2006          25(4)          22-25
Studies on the chemical constituents of the sea pen Cavernularia sp.
DUAN Lin, FAN G Yu-chuan, ZHU Wei-ming, GU Qian-qun, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     µ¨çÞ-5-Ï©-3¦Â,7¦Â¶þ´¼
C27H46O2     ÏàËÆ¶È:75%
Chinese Journal of Marine Drugs          2004          23(1)          1-5
Polyhydroxy sterols from soft coral Dendronephthya gigantea from the South China Sea
LI Guo-qiang, DENG Zhi-wei, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     cholesterol
    ÏàËÆ¶È:75%
Natural Product Research          2012          26          774-777
Sterols from Sargassum oligocystum, a brown algae from the Persian Gulf, and their bioactivity
Parisa Permeh, Soodabeh Saeidnia, Ali Mashinchian-Moradi and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     cholesterol
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2010          35          2412-2415
Chemical constituents of Gekko swinhonis
LI Wen; WANG Guocai; ZHANG Xiaoqi; WANG Ying; YE Wencai;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     cholesterol
    ÏàËÆ¶È:75%
Steroids          1994          59          310-317
Inhibitors of sterol synthesis. Effects of fluorine substitution at carbon atom 25 of cholesterol on its spectral and chromatographic properties and on 3-hydroxy-3-methylglutaryl coenzyme a reductase activity in CHO-K1 cells
William K. Wilson, Shankar Swaminathan, Frederick D. Pinkerton, Nicolas Gerst, George J. Schroepfer Jr.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     cholesterol
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     3-hydroxycholest-5-en-24-one
C27H44O2     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2007          38          356-357
Ã××ÐÀ¼»¯Ñ§³É·ÖÑо¿
ÀîÏþÃ÷;Áõ½¡ÃÀ;ÕÅÒí;Íõ±ó¹ó
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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57 .     cholesterol
C27H46O     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2004          35          485-487
Study on chemical constituents of Trachyrhamphus serratus
HUANG Jian-she; LI Qing-xin; WU Jun; ZHANG Si
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     choleserol
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          1994          25          229-231+265+278
Studies on the Chemical Constituents of the Pilose Antler of Red Deer (Cervus elaphus)
Yang Xiuwei and Bai Yunpeng(Jilin Provincial College of Traditional Chinese Medicine and Materia Medica; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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59 .     cholesterol
C27H46O2     ÏàËÆ¶È:75%
Chinese Journal of Natural Medicines          2004          2          348-350
Studies on Chemical Constituents of Acaudina molpadioides Semper
ZOU Zheng-Rong; YI Yang-Hua; YAO Xin-Sheng; DU Li-Jun; ZHOU Da-Zheng; ZHANG Shu-Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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60 .     fucosterol
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2003          26          719-722
Anti-oxidant activities of fucosterol from the marine algae Pelvetia siliquosa
Sanghyun Lee, Yeon Sil Lee, Sang Hoon Jung, Sam Sik Kang and Kuk Hyun Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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61 .     cholesterol
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2004          27          734-737
Cytotoxic constituents of diadema setosum
Chau Van Minn, Phan Van Kiem, Le Mai Huong and Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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62 .     24-ketocholesterol
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2002          37          262-265
Studies on the bioactive steroid constituents from Sargassum carpophyllum
TANG Hai-feng, YI Yang-hua, YAO Xin-sheng, ZHOU Da-zheng, LÜ Tai-sheng, JIANG Yong-pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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63 .     cholesterol
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2010          45          647-649
Liposoluble Constituents of Gorgonian Subergorgia suberosa from South China Sea
JIAN Shui-lian, LIAO Xiao-jian, XU Shi-hai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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64 .     µ¨çÞ´¼
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2010          45          172-174
Isolation and Structure Identification of Several Chemical Constituents in Gorgonian Verrucella sp.
WANG Wei, XU Shi-hai*, LIAO Xiao-jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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65 .     cholestero
    ÏàËÆ¶È:75%
Journal of Shenyang Pharmaceutical University          2009          26          523-535
Chemical constituents of Selaginella tamariscina (Beauv.) Spring
WANG Xue, LI Zhan-lin, GAO Liang-liang, LI Jin-nan, HUA Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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66 .     cholesterol
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          2011          47          114-115
Flavonoid and other compounds from Holotrichia diomphalia larvae
Q. F. Dong, Z. Wang, H. J. Liu, C. F. Zhang and D. X. He, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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67 .     cholesterol
    ÏàËÆ¶È:75%
Chinese Journal of Natural Medicines          2011          9          33-37
Chemical Constituents of Saussurea eopygmaea
ZHANG Bei-Bei, DAI Yuan, LIAO Zhi-Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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68 .     cholesterol
    ÏàËÆ¶È:75%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1982          21(1)          71-77
Studies on the Chinese Soft Corals (VI)
Long Kanghou Luo Yunkang Fang Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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69 .     cholesterol
    ÏàËÆ¶È:75%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1993          32(2)          90-92
Studies on the Marine Sponge Hircinia variabilis
Meng Yanhui Su Jingyu Zeng Longmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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70 .     chloesterol
    ÏàËÆ¶È:75%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1999          38(5)          118-120
Structural Determination of Lobophytol A Isolated from the Soft Coral
CHEN Cheng-sheng, FU Shi-liang, JIA Min-sha, ZENG Long-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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71 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:75%
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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72 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:75%
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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