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²éѯ½á¹û£º¹²²éµ½244¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
2Â¥2013-09-26 07:41:23
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ralonxu: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-09-26 09:20:04
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²éѯ½á¹û£º¹²²éµ½4355¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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