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1 .     (7R*)-opposit-4(15)-ene-1¦Â,7-diol
C15H26O2     ÏàËÆ¶È:100%
Chemical & Pharmaceutical Bulletin          2003          51(5)          545-549
Five New Sesquiterpenoids and a New Diterpenoid from Erigeron annuus (L.) PERS., Erigeron philadelphicus L. and Erigeron sumatrensis RETZ.
Takeyoshi IIJIMA, Yasunori YAOITA, and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     octahydro-4-hydroxy-3¦Á-methyl-7-methylene-¦Á-(1-methylethyl)-1H-indene-1-methanol
     ÏàËÆ¶È:100%
Journal of Natural Products          2003          66          609-615
New Sesquiterpenes from Litsea verticillata
Hong-Jie Zhang, Ghee Teng Tan, Bernard D. Santarsiero, Andrew D. Mesecar, Nguyen Van Hung, Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, and Harry H. S. Fong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     octahydro-4-hydroy-3¦Á-methyl-7-methylene-¦Á-(1-methylethyl)-1H-indene-1-methanol
     ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2009          34          2891-2894
Chemical constituents from Piper longum
LIU Wenfeng, JIANG Zhiyong, CHEN Jijun, ZHANG Xuemei, MA Yunbao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (7R)-opposit-4(15)-ene-1¦Â,7-diol
C15H26O2     ÏàËÆ¶È:100%
Chemistry & Biodiversity          2011          8          643-650
Antiproliferative Compounds of Cyphostemma greveana from a Madagascar Dry Forest
Shugeng Cao, Yanpeng Hou, Peggy Brodie, James S. Miller, Richard Randrianaivo, Etienne Rakotobe, Vincent E. Rasamison and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     eudesm-4(15)-ene-1¦Â,8¦Á-diol
C15H26O2     ÏàËÆ¶È:100%
Chinese Journal of Organic Chemistry          2004          24          806-810
Sesquiterpenes from Caragana Intermedia
SUN, Zhi-Hua ZHANG, Su SHI, Jiao HU, Chang-Qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     7¦Ä-Methoxy-4(14)-oppositen-1¦Â-ol
     ÏàËÆ¶È:75%
Archives of Pharmacal Research          2007          30          1067-1074
Lignan and terpene constituents from the aerial parts of saussurea pulchella
Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Leptocladolin A
C17H28O3     ÏàËÆ¶È:70.5%
Bulletin of the Chemical Society of Japan          2010          83          678-682
Oppositane-Type Sesquiterpenoids from the Formosan Soft Coral Sinularia leptoclados
Chiung-Yao Huang, Jui-Hsin Su, Yung-Chun Liu, Zhi-Hong Wen, Chi-Hsin Hsu, Michael Y. Chiang, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (7R*)-opposit-4(15)-ene-7-acetoxy-1¦Â-ol
C17H28O3     ÏàËÆ¶È:70.5%
Chemistry & Biodiversity          2011          8          643-650
Antiproliferative Compounds of Cyphostemma greveana from a Madagascar Dry Forest
Shugeng Cao, Yanpeng Hou, Peggy Brodie, James S. Miller, Richard Randrianaivo, Etienne Rakotobe, Vincent E. Rasamison and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     ent-4(15)-eudesmene-1¦Â,6¦Á-diol
C15H26O2     ÏàËÆ¶È:66.6%
Phytochemistry          2005          66          1662-1670
ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica
Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4(15)-eudesmene-1¦Â,6¦Á-diol
C15H24O     ÏàËÆ¶È:66.6%
Phytochemistry          2003          64          303-323
Terpenoids from the seeds of Artemisia annua
Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-26 07:41:23
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1 .     24E-ergosta-7,22-dien-6-one-3¦Â,5¦Á-diol
C28H44O3     ÏàËÆ¶È:92.5%
Natural Product Research and Development          1992          4(2)          44-47
CHEMICAL RESEARCH ON THE METABOLITES OF LACTARIUS HYSGINUS (¢ñ)
Dong Ding* Wang Huaibin Li Guangyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3,5-dihydroxyergosta-7,22-dien-6-one
C28H44O3     ÏàËÆ¶È:88.8%
Mycosystema          2009          28          407-409
Chemical components from the fruiting bodies of Ganoderma duropora
ZHAO Fen LI Ye LIU Chao LI Bao-Ming CHEN Ruo-Yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     3¦Â,5¦Á-Dihydroxy-ergosta-7,22-diene
     ÏàËÆ¶È:85.1%
Archives of Pharmacal Research          2002          25          851-855
Cytotoxic ergosterols from paecilomyces sp. J300
Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 8
     ÏàËÆ¶È:82.1%
Chinese Journal of Chemistry          2003          21          1390-1394
Sterols from the fungus Catathelasma imperiale
Sheng-Ping Yang, Jun Xu and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
     ÏàËÆ¶È:81.4%
Chinese Traditional and Herbal Drugs          2011          42          31-33
Chemical constituents of Dendrobium crystallinum
WANG Lei, ZHANG Chao-feng, WANG Zheng-tao, ZHANG Mian, XU Luo-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (24R)-24-methyl-5¦Á-cholest-7-ene-3¦Â,5,6¦Â-triol
C28H46O2     ÏàËÆ¶È:80.7%
Journal of Natural Products          1989          Vol 52          952
New Polyhydrozysterols fron the Di tyoceratid Sponges Hippospongia Communis, Spongia officinalis, Ircinia Variabilis, and Spongionella gracilis
Anna Madaio, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     cerevisterol
     ÏàËÆ¶È:78.5%
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

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8 .     (24S)-ergosta-7-ene-3¦Â, 5¦Á, 6¦Â-triol
C28H48O3     ÏàËÆ¶È:78.5%
Acta Botanica Yunnanica          2000          22(1)          85-89
The Constituents of the Basidiomycetes Russula cyanoxantha
GAO Jin-Ming, DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol
     ÏàËÆ¶È:78.5%
Biochemical Systematics and Ecology          2007          35          790-793
Triterpenes and steroids from Armillaria mellea Vahl. ex Fr.
Wen-Juan Guo, Shun-Xing Guo, Jun-Shan Yang, Xiao-Mei Chen, Pei-Gen Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     5,6-Epoxy-22-en-3-ol-ergosterol
C28H44O2     ÏàËÆ¶È:78.5%
Chemical Research in Chinese Universities          1998          14          270-272
Chemical Constituent of Natural Body of Armillaria mellea and Structure of 5, 6-Epoxy-22-en-3-ol-ergosterol
SHI Lei, CAO Rui-min, LU Shi-xiang and WU Guang-xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-09-26 07:43:22
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