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12.1,13.9,14.6,16.3,17.6,18.9,19.6,19.8,20.1,20.4,21.1,23.3,23.8,24.5,25.7,27.6,27.7,29.3,29.7,31.0,32.5,32.9,34.8,36.6,37.3,39.3,40.2,40.4,44.1,52.9,65.9,66.2,74.7,76.1,77.4,120.8,127.2,128.8,130.9,133.7,140.0,141.0,141.9,167.7,170.7,173.8,178.1,196.9
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²éѯ½á¹û£º¹²²éµ½466¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     3b-linoleyloxyergost-7-ene
    ÏàËÆ¶È:64.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
    ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3b-linoleyloxyergosta-7,22-diene
    ÏàËÆ¶È:62.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     pentacetylfusapyrone
    ÏàËÆ¶È:62.5%
Natural Toxins          1994          2          4-13
Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum
Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid
C45H78O4     ÏàËÆ¶È:62.5%
Life Sciences          2013          92          202-210
Antiulcer and antioxidant activities of a new steroid from Morus alba
Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch
C54H77NO8     ÏàËÆ¶È:61.2%
The Journal of Organic Chemistry          2012          77          3297-3310
Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin
Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
C46H76O4     ÏàËÆ¶È:60.4%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     georgamide
C46H69O10N5     ÏàËÆ¶È:60.4%
Journal of Natural Products          2001          64          143-146
Georgamide, a New Cyclic Depsipeptide with an Alkynoic Acid Residue from an Australian Cyanobacterium
Feng Wan and Karen L. Erickson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     xanthanthusin B
C44H52O12     ÏàËÆ¶È:60.4%
Acta Botanica Yunnanica          1993          15(4)          403-407
DITERPENOID QUINONES FROM COLEUS XANTHANTHUS
LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate
C53H96O3Si     ÏàËÆ¶È:60.4%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     iristectorene A monoacetate
    ÏàËÆ¶È:60.4%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3-O-(4'-benzhydryloxy-3',3'-dimethylsuccinyl)-28-O-glutarylbetulin
C54H74O8     ÏàËÆ¶È:60.4%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-(5'-benzhydryloxygluta-ryl)-28-O-(2'',2''-dimethylsuccinyl)dihydrobetulin
C54H76O8     ÏàËÆ¶È:60.4%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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²éѯ½á¹û£º¹²²éµ½466¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------

1 .     3b-linoleyloxyergost-7-ene
    ÏàËÆ¶È:64.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
    ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     3b-linoleyloxyergosta-7,22-diene
    ÏàËÆ¶È:62.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     pentacetylfusapyrone
    ÏàËÆ¶È:62.5%
Natural Toxins          1994          2          4-13
Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum
Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid
C45H78O4     ÏàËÆ¶È:62.5%
Life Sciences          2013          92          202-210
Antiulcer and antioxidant activities of a new steroid from Morus alba
Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch
C54H77NO8     ÏàËÆ¶È:61.2%
The Journal of Organic Chemistry          2012          77          3297-3310
Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin
Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
C46H76O4     ÏàËÆ¶È:60.4%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     georgamide
C46H69O10N5     ÏàËÆ¶È:60.4%
Journal of Natural Products          2001          64          143-146
Georgamide, a New Cyclic Depsipeptide with an Alkynoic Acid Residue from an Australian Cyanobacterium
Feng Wan and Karen L. Erickson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     xanthanthusin B
C44H52O12     ÏàËÆ¶È:60.4%
Acta Botanica Yunnanica          1993          15(4)          403-407
DITERPENOID QUINONES FROM COLEUS XANTHANTHUS
LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate
C53H96O3Si     ÏàËÆ¶È:60.4%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     iristectorene A monoacetate
    ÏàËÆ¶È:60.4%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     3-O-(4'-benzhydryloxy-3',3'-dimethylsuccinyl)-28-O-glutarylbetulin
C54H74O8     ÏàËÆ¶È:60.4%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     3-O-(5'-benzhydryloxygluta-ryl)-28-O-(2'',2''-dimethylsuccinyl)dihydrobetulin
C54H76O8     ÏàËÆ¶È:60.4%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     3-O-(5'-benzhydryloxyglutaryl)-28-O-glutaryldihydro-betulin
C53H74O8     ÏàËÆ¶È:60.4%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     6'-linoleic-¦Â-daucosterol
C30H50O     ÏàËÆ¶È:60.4%
Natural Product Research and Development          2009          21          776-778
Chemical Constituents of the Roots of Ligularia fischeri
DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl3-acetoxy-2-((S)-2,3-dimethyl-2-(methylamino)butoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)chrysene-7-carboxylate
C46H71NO6     ÏàËÆ¶È:60.4%
The Journal of Organic Chemistry          2012          77          3297-3310
Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin
Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-3-Acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)chrysene-
C47H71NO8     ÏàËÆ¶È:60.4%
The Journal of Organic Chemistry          2012          77          3297-3310
Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin
Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     compound 23
C52H86N8O12     ÏàËÆ¶È:60%
Journal of Natural Products          2003          66          1356-1363
Isolation and Structure Determination of Lyngbyastatin 3, a Lyngbyastatin 1 Homologue from the Marine Cyanobacterium Lyngbya majuscula.Determination of the Configuration of the 4-Amino-2,2-dimethyl-3-oxopentanoic Acid Unit in Majusculamide C, Dolastatin 1
Philip G. Williams,Richard E. Moore,and Valerie J. Paul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     leucinostatin A hydrochloride
C62H111N11O13     ÏàËÆ¶È:58.8%
The Journal of Antibiotics          1983          36          1606-1612
STUDIES ON PEPTIDE ANTIBIOTICS, LEUCINOSTATINS I. SEPARATION, PHYSICO-CHEMICAL PROPERTIES AND BIOLOGICAL ACTIVITIES OF LEUCINOSTATINS A AND B
KAZUTAKA FUKUSHIMA, TADASHI ARAI, YUJI MORI, MAKOTO TSUBOI, MAKOTO SUZUKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     Benzyl oleanolate 3-O-2,3,4,6-tetra-O-acetyl-¦Á-D-mannopyranoside
C51H72O8     ÏàËÆ¶È:58.8%
Molecules          2011          16          1113-1128
Synthesis and Anti-Fungal Activity of Seven Oleanolic Acid Glycosides
Hanqing Zhao, Guanghui Zong, Jianjun Zhang, Daoquan Wang and Xiaomei Liang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate
    ÏàËÆ¶È:58.3%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     homodolastatin 16
C48H72N6O10     ÏàËÆ¶È:58.3%
Journal of Natural Products          2003          66          712-715
Isolation of Homodolastatin 16, a New Cyclic Depsipeptide from a Kenyan Collection of Lyngbya majuscula
Michael T. Davies-Coleman, Thomas M. Dzeha, Christopher A. Gray, Sonja Hess, Lewis K. Pannell, Denver T. Hendricks, and Catherine E. Arendse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     compound 27
C50H82N8O11     ÏàËÆ¶È:58.3%
Journal of Natural Products          2003          66          1356-1363
Isolation and Structure Determination of Lyngbyastatin 3, a Lyngbyastatin 1 Homologue from the Marine Cyanobacterium Lyngbya majuscula.Determination of the Configuration of the 4-Amino-2,2-dimethyl-3-oxopentanoic Acid Unit in Majusculamide C, Dolastatin 1
Philip G. Williams,Richard E. Moore,and Valerie J. Paul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     gymnasterone A
C45H67NO5     ÏàËÆ¶È:58.3%
Journal of Natural Products          2007          70          1731-1740
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     3-O-tetradecanoyl-16-O-acetylisoiridogermanal
C46H78O6     ÏàËÆ¶È:58.3%
Journal of Natural Products          1999          62          89-93
Iridal-Type Triterpenoids with Ichthyotoxic Activity from Belamcanda chinensis
Hideyuki Ito, Satomi Onoue, Yoko Miyake, and Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     xanthanthusin C
C44H52O12     ÏàËÆ¶È:58.3%
Acta Botanica Yunnanica          1993          15(4)          403-407
DITERPENOID QUINONES FROM COLEUS XANTHANTHUS
LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene
C37H66O3Si     ÏàËÆ¶È:58.3%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     Iristectorene B monoacetate
C46H78O6     ÏàËÆ¶È:58.3%
Phytochemistry          1994          36          433-438
Iristectorene B, a monocyclic triterpene ester from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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29 .     BRM-14
C46H70BO15     ÏàËÆ¶È:58.3%
Heterocycles          2010          82          289-295
Boromycin Derivatives: Synthesis and Antimalarial Activity in vitro and in vivo
Ayumi Tsutsui, Yujiro Furuya, Tomoyasu Hirose, Riyon Kim, Rokurou Masuma, Atsuko Matsumoto, Yoko Takahashi, Aki Ishiyama, Miyuki Namatame, Kazuhiko Otoguro, Satoshi ¨­mura, and Toshiaki Sunazuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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30 .     Compound 7
C33H37N4O3F     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry Letters          1997          7          799-804
Synthesis and evaluation of halogenated dibenzodiazepines as muscarinic receptor ligands
Michael Kassiou, Roger W. Read, Xue-qin Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     3b-linoleyloxyergost-7-ene
    ÏàËÆ¶È:64.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3-O-[6'-O-n-acyl-¦Â-D-glucosyl]-22-dehydroclerosterol
    ÏàËÆ¶È:64.5%
Phytochemistry          1994          36          167-170
Acylglucosylsterols from two Aegiphila species
Suzana G. Leitão, Maria Auxiliadora C. Kaplan, Franco Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
    ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3b-linoleyloxyergosta-7,22-diene
    ÏàËÆ¶È:62.5%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     pentacetylfusapyrone
    ÏàËÆ¶È:62.5%
Natural Toxins          1994          2          4-13
Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum
Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid
C45H78O4     ÏàËÆ¶È:62.5%
Life Sciences          2013          92          202-210
Antiulcer and antioxidant activities of a new steroid from Morus alba
Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch
C54H77NO8     ÏàËÆ¶È:61.2%
The Journal of Organic Chemistry          2012          77          3297-3310
Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin
Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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