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13C NMR (101 MHz, CDCl3) ¦Ä 187.92, 187.46, 144.68, 140.77, 140.67, 140.41, 131.12, 129.07, 72.91, 65.79, 42.53, 40.49, 39.60, 37.84, 37.66, 37.52, 33.03, 33.00, 30.80, 29.92, 28.20, 26.81, 25.02, 24.72, 22.93, 22.84, 21.63, 21.54, 19.97, 19.92, 19.41, 13.94, 12.58, 12.50, 12.18.
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¶¹¸ç: ½ð±Ò+2, лл 2012-09-02 08:33:36
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
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2Â¥2012-09-02 07:42:06
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Òø³æ (ÕýʽдÊÖ)

ÒýÓûØÌû:
2Â¥: Originally posted by »ð¼ý´©Æ¨Æ¨ at 2012-09-02 07:42:06
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
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13C NMR (101 MHz, CDCl3) ¦Ä 12.18,12.50,12.58,13.94,19.41,19.92,19.97,21.54,21.63,22.84,
22.93,24.72,25.02,26.81,28.20,29.92,30.80,33.00,33.03,37.52,
37.66,37.84,39.60,40.49,42.53,65.79,72.91,129.07,131.12,
140.41,140.67,140.77,144.68,187.46,187.92
3Â¥2012-09-02 20:49:26
ÒÑÔÄ   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

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¶¹¸ç: ½ð±Ò+4, лл 2012-09-03 08:28:32
ħÁ¦Äñ: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, thank u ! 2012-09-03 08:32:53
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1 .     ¦Á-tocopherolquinone methyl ether
C30H50O3     ÏàËÆ¶È:80%
Phytochemistry          1991          30          2800-2803
A benzoquinone and a coumestan from Psoralea plicata
Nazli Rasool, Abdul Qasim Khan, Viqar Uddin Ahmad, Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     3¦Â-Acetoxysitost-5-ene-7¦Á-ol
C31H52O3     ÏàËÆ¶È:65.7%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     24-methylenecholesterol palmitate
C44H76O2     ÏàËÆ¶È:62.8%
Phytochemistry          2008          69          2061-2066
Antioxidant constituents of Nymphaea caerulea flowers
Vijai K. Agnihotri, Hala N. ElSohly, Shabana I. Khan, Troy J. Smillie, Ikhlas A. Khan, Larry A. Walker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     22-dihydrospinasterol
    ÏàËÆ¶È:62.8%
Phytochemistry          1981          20          761-764
Co-occurrence of chondrillasterol and spinasterol in two cucurbitaceae seeds as shown by 13C NMR
Toshihiro Itoh, Yoshinori Kikuchi, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     22-dihydrospinasterol
    ÏàËÆ¶È:62.8%
Phytochemistry          1982          21          727-730
Co-occurrence of c-24 epimeric 24-ethyl-¦¤7 -sterols in the roots of Trichosanthes japonica
T. Itoh, K. Yoshida, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     1,6-dimethyl-4-((3R,7R,11R)-3-hydroxy-3,7,11,15-tetramethylhexadecyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-ylacetate
C31H54N2O3     ÏàËÆ¶È:62.8%
Bioorganic & Medicinal Chemistry          2010          18          7628-7638
Design, synthesis, and evaluation of an ¦Á-tocopherol analogue as a mitochondrial antioxidant
Jun Lu, Omar M. Khdour, Jeffrey S. Armstrong, Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     3-[2-Methyl-5-(1-methylethyl)-3,6-dioxocyclohexa-1,4-dienyl)propyl Betulinate
    ÏàËÆ¶È:62.1%
Chemistry & Biodiversity          2010          7          129-139
Terpene Conjugates of the Nigella sativa Seed-Oil Constituent Thymoquinone with Enhanced Efficacy in Cancer Cells
Katharina Effenberger, Sandra Breyer and Rainer Schobert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     (+)-¦Á-Tocopheryl 2,3,4,6-tetra-O-acetyl--D-galactopyranoside
    ÏàËÆ¶È:61.1%
Zeitschrift f¨¹r Naturforschung B          2002          57          571-578
Studies in the Acid Catalysed Glycosylation of a-Tocopherol
S. Witkowski and P. Wa£jko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     dehydro-¦Ã-tocopherol
C28H46O2     ÏàËÆ¶È:60%
Phytochemistry          2004          65          2719-2729
Antioxidant dehydrotocopherols as a new chemical character of Stemona species
Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     stigmast-5-ene-3¦Â,4¦Â-diyl
C31H50O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     compound 2
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     alisol N-23-acetate
C32H50O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1999          47          524-528
Studies on Alismatis Rhizoma. III. Stereostructures of New Protostane-Type Triterpenes, Alisols H, I, J-23-Acetate, K-23-Acetate, L-23-Acetate, M-23-Acetate, and N-23-Acetate, from the Dried Rhizome of Alisma orientale
Masayuki YOSHIKAWA,Norimichi TOMOHIRO,Toshiyuki MURAKAMI,Akira IKEBATA,Hisashi MATSUDA,Hideaki MATSUDA and Michinori KUBO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     (24R,241R)-24(241)-epoxyisoavenasteryl acetate
    ÏàËÆ¶È:60%
Phytochemistry          1999          52          1601-1605
(24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica
Toshihiro Akihisa, Yumiko Kimura, Kazuo Koike, Wilhelmus C.M.C. Kokke, Tadashi Ohkawa, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     (24S,241S )-24(241)-epoxyisoavenasteryl acetate
    ÏàËÆ¶È:60%
Phytochemistry          1999          52          1601-1605
(24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica
Toshihiro Akihisa, Yumiko Kimura, Kazuo Koike, Wilhelmus C.M.C. Kokke, Tadashi Ohkawa, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     sasanquyl acetate
C32H54O2     ÏàËÆ¶È:60%
Phytochemistry          1998          48          301-305
Sasanquol, A 3,4-seco-triterpene alcohol from sasanqua oil, and its anti-inflammatory effect
Toshihiro Akihisa, Kem Yasukawa, Yumiko Kimura, Sakae Yamanouchi, Toshitake Tamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     ergosteryl myristate
C42H70O2     ÏàËÆ¶È:60%
Natural Product Sciences          1999          5          93-96
Ergosteryl Myristate, a New Ergosterol Derivative from Unidentified Marine Algicolous Fungus
Lee, Dong-Ick; Choi, Jin-Souk; Yang, Mi-Rim; Lee, Won-Kap; Kim, Dong-Soo; Choi, Hong-Dae; Son, Byeng-Wha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     stigmasterol tritriacontanate
C62H112O2     ÏàËÆ¶È:60%
Chinese Herbal Medicines          2011          3          244-246
A New Stigmasterol Ester from Aeschynomene indica
CHEN Jia-yuan, TAN Xiao, LU Wen-jie, YA Qi-kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     (22R,23R)-3¦Â,22,23-Triacetoxystigmast-5-ene
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     (22R,23R)-3¦Â-Hydroxy-22,23-isopropylidenedioxy-stigmast-5-en
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     3b(2-p-tolyolsulfonyloxy)-ethoxycholest-5-ene
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2010          20          2872-2875
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:60%
Phytochemistry          1981          20          761-764
Co-occurrence of chondrillasterol and spinasterol in two cucurbitaceae seeds as shown by 13C NMR
Toshihiro Itoh, Yoshinori Kikuchi, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:60%
Phytochemistry          1982          21          727-730
Co-occurrence of c-24 epimeric 24-ethyl-¦¤7 -sterols in the roots of Trichosanthes japonica
T. Itoh, K. Yoshida, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     Stosterol
    ÏàËÆ¶È:60%
Natural Product Research          2010          24          34-39
A new analogue of fatty alcohol from Tamarix hampeana L.
Ahmet Aykaç; Yurdanur Akg¨¹l
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     sitost-5-en-3¦Â-ol acetate
C31H52O2     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2010          41          1052-1056
Chemical constituents from stems of Melicope pteleifolia
LI Shuo-guo; YANG Yin; YE Wen-cai; JIANG Ren-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     Crassumtocopherol B
C31H52O6     ÏàËÆ¶È:60%
Bulletin of the Chemical Society of Japan          2011          84          783-787
¦Á-Tocopherols from the Formosan Soft Coral Lobophytum crassum
Shi-Yie Cheng, Shih-Tseng Lin, Shang-Kwei Wang, Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     ¡÷7-stigmasteryl-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:60%
Natural Product Research and Development          1997          9(1)          40-42
CHEMICAL COMPONENTS FROM BERNEUXIA THIBETICA DECNE
Wang Mingkui; Ding Lisheng and Wu Fenge
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     5-oxo-5-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]pentanoic acid
C34H54O4     ÏàËÆ¶È:60%
Molecules          2011          16          9340-9356
Communication: Consecutive Three-Component Synthesis of 3-(Hetero)Aryl-1H-pyrazoles with Propynal Diethylacetal as a Three-Carbon Building Block
Lucilla Levi, Christina Boersch, Charlotte F. Gers, Eugen Merkul and Thomas J. J. M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     ¦Â-daucosterol
C35H60O6     ÏàËÆ¶È:60%
Chinese Journal of Natural Medicines          2011          9          176-179
Chemical Constituents from the Stems of Ilex pubescens var. glabra
LIN Li-Ping, QU Wei, LIANG Jing-Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     (22E,24R)-6-(1,3-Dioxolan-2-yl)-26-methanesulfonyloxy-24-methyl-3¦Á,5-cyclo-5¦Á-cholest-22-ene
    ÏàËÆ¶È:58.9%
Steroids          2012          77          780-790
A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursorsOriginal Research Article
Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     4-Butyl-5-N-cyclohexylcarboxamido-4-aza-5¦Â-cholestan-3-one
C37H64N2O2     ÏàËÆ¶È:58.3%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     ergosta-7,11-dien-3¦Â-yl palmitate
C44H76O2     ÏàËÆ¶È:57.8%
Phytochemistry          1990          29          673-675
A lanostanoid of formosan Ganoderma lucidum
Chun-Nan Lin,Whey-Pin Tome,Shen-Jeu Won
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     cholesta-3,5-diene
    ÏàËÆ¶È:57.8%
Journal of the Korean Chemical Society          1991          35          249-252
The Chemical Constituents of Bezoar Bovis
In Kyu Kim, Sun Ku Park, Hyun Cheol Oh, Kyu Wan Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     ulmudiol
C30H50O2     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2006          54(6)          775-778
New Triterpenoids Isolated from the Root Bark of Ulmus pumila L.
Dong WANG,Mingyu XIA,and Zheng CUI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     dehydroulmudiol
C30H48O2     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2006          54(6)          775-778
New Triterpenoids Isolated from the Root Bark of Ulmus pumila L.
Dong WANG,Mingyu XIA,and Zheng CUI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     calocedimer B
C35H54O     ÏàËÆ¶È:57.1%
Journal of Natural Products          2006          69          665-667
Calocedimers A, B, C, and D from the Bark of Calocedrus macrolepis var. formosana
Chin-Lin Hsieh, Lung-Lin Shiu, Mei-Huims Tseng, Yi-Yuan Shao, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     ferrugieudesmol
C35H54O2     ÏàËÆ¶È:57.1%
Journal of Natural Products          2006          69          1611-1613
C35 Terpenoids from the Bark of Calocedrus macrolepis var.formosana with Activity against Human Cancer Cell Lines
Chin-Lin Hsieh, Mei-Huims Tseng, Yi-Yuan Shao, Jang-Yang Chang, Ching-Chuan Kuo, Chi-Yen Chang, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     fomlactone A
C33H50O5     ÏàËÆ¶È:57.1%
Journal of Natural Products          2003          66          1249-1251
Fomlactones A-C, Novel Triterpene Lactones from Fomes cajanderi
Jian He,Xiao-Zhang Feng, Yang Lu, and Bin Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     24-methylene cholest-5-en-1¦Á,3¦Â,19-triol-1,3,19-triacetate
C34H52O6     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1584-1585
Two New 19-Oxygenated Polyhydroxy Steroids from the Soft Coral Nephthea chabroli
M. Rama Rao, U. Venkatesham, and Y. Venkateswarlu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     ¦Â-sitosterol benzoate
    ÏàËÆ¶È:57.1%
Planta Medica          1988          54          223-224
Antihepatotoxic Principles of Sambucus formosana
Chun-Nan Lin and Whey-Pin Tome
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     stigmastane-3¦Â,6¦Á-diyl
C33H56O4     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     poriferastane-3¦Â,6¦Á-diyl diacetates
C33H56O4     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     poriferast-5-ene-3¦Â,4¦Â-diyl diacetate
C31H50O2     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     poriferasta-5,25-diene-3¦Â,4¦Â-diyl diacetate
C33H52O4     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     N-[3-oxolup-20(29)-en-28-oyl]-n-butylamine
C34H55NO2     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2008          44          327-333
SYNTHESIS OF BETULONIC ACID AMIDES
A. N. Antimonova, N. V. Uzenkova, N. I. Petrenko,M. M. Shakirov, E. E. Shul¡äts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     ¦Â-Daucosterin
    ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2007          43          355-357
CHEMICAL CONSTITUENTS OF Bacopa monnieri
Y. Zhou Y.-H. Shen, C. Zhang, and W.-D. Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     3-O-¦Â-D-Glucopyranosyl Stigmasterol
C35H57O     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2004          40          137-140
PHYTOCHEMICAL STUDIES OF Berberis vulgaris
S. Saied and S. Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     (1S,4R,5R,8R,9S,12R,13S),12-(1S-Hydroxyethyl)-13-(-benzyl-2-carboxamidoEthyl)-5-(1,5-dimethylhexyl)-1,9-epoxy-4,8,13-trimethyl Tricyclo [7,4,0,0,4,8] Tridecane
    ÏàËÆ¶È:57.1%
Molecules          2001          6          M222
(1S, 4R, 5R, 8R, 9S, 12R, 13S), 12-(1S-Hydroxyethyl)-13-( -benzyl-2-carboxamidoEthyl)-5-(1, 5-dimethylhexyl)-1, 9-epoxy-4, 8, 13-trimethyl Tricyclo [7, 4, 0, 0, 4, 8] Tridecane
M. Daoubi, A. Benharref1 and Diego. M. Cortes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     (22E)-3¦Â-Acetoxy-5¦Á-stigmast-22-en-6-one
    ÏàËÆ¶È:57.1%
Steroids          2000          65          329-337
Synthesis and bioactivity evaluation of brassinosteroid analogs
Javier A. Ram¨ªrez, Osvaldo M. Teme Centuri¨®n, Eduardo G. Gros, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     3¦Â-(tert-butyldimethylsilanyloxy)-cholest-5-en-7¦Â-ol
C33H60O2Si     ÏàËÆ¶È:57.1%
Steroids          2003          68          192-198
Synthesis of (20S)-[7,7,21,21-2H4]-3¦Â-(tert-butyldimethylsilanyloxy)-20-methyl-pregn-5-en-21-ol, a useful intermediate for the preparation of deuterated isotopomers of sterols
Pierangela Ciuffreda, Silvana Casati, Deborah Bollini, Enzo Santaniello
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     (22E,24R)-24-(1-Buten-2-yl)-6¦Â-methoxy-3¦Á,5-cyclo-5¦Á-cholest-22-ene
C32H52O     ÏàËÆ¶È:57.1%
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
--------------------------------------------------------------------------------

51 .     (22E,24S)-24-(1-Buten-2-yl)-6¦Â-methoxy-3¦Á,5-cyclo-5¦Á-cholest-22-ene
C33H54O3     ÏàËÆ¶È:57.1%
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
--------------------------------------------------------------------------------

52 .     (20R,22Z)-3¦Â-(tert-Butyldimethylsilyl)oxycholesta-5,22-dien-20-ol
C33H58O2Si     ÏàËÆ¶È:57.1%
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
--------------------------------------------------------------------------------

53 .     6-Methoxy-3,4-dehydro-¦Ä-tocopherol
C28H46O2     ÏàËÆ¶È:57.1%
Journal of Asian Natural Products Research          2007          9          509-515
Antibacterial constituents from Stemona sessilifolia
TONG ZHANG, YA-ZHONG ZHANG and JIAN-SHENG TAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

54 .     ¦Á-spinasterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          1997          22          293-295
Separation and Identification of the Compounds from A chyranthes biden tata Bl
W ei Song, L iang Hong, Zhao Yuying and Zhang Ruyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

55 .     daucosterol
    ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          1997          22          293-295
Separation and Identification of the Compounds from A chyranthes biden tata Bl
W ei Song, L iang Hong, Zhao Yuying and Zhang Ruyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

56 .     stigma-¦¤7,22-dien-3¦Â-palmitate
C45H78O2     ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          1996          21          483-484
A Study on the Chemical Contituents of Aster albscens Hand. -Mazz.
He Lan and Cheng Dongliang, Pan Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

57 .     24-ethyl-4¦Á-methyl-cholestane-3,20-diol
C30H45O2     ÏàËÆ¶È:57.1%
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
--------------------------------------------------------------------------------

58 .     ¦Á-spinasterol octadecanonate
C47H82O2     ÏàËÆ¶È:57.1%
Acta Pharmaceutica Sinica          1998          Vol 33          839-842
TRITERPENES AND STEROIDAL COMPOUNDS FROM MOMORDICA DIOICA
Luo Lei(Luo L) ; Li Zuqiang(Li ZQ); Zhang Yuanqing(Zhang YQ) and Huang Rong(Huang R)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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