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mengbuluo: ½ð±Ò+10 2014-04-18 13:49:23
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mengbuluo: ½ð±Ò+10 2014-04-18 13:49:23
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1 . (3b)-3-(acetyloxy)lanosta-7,9(11),24-trien-21-oic acid C32H48O4 ÏàËÆ¶È:100% Helvetica Chimica Acta 2013 96 2092-2097 Lanostane Triterpenes from Ceriporia lacerate HS-ZJUT-C13A, a Fungal Endophyte of Huperzia serrata You-Min Ying, Wei-Guang Shan, Li-Wen Zhang, Yan Chen and Zha-Jun Zhan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 4a ÏàËÆ¶È:81.2% Journal of Natural Products 1986 Vol 49 1122 Two New Lanostanoids from Ganoderma lucidum Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Dehydroeburicoic acid monoacetate ÏàËÆ¶È:78.7% Phytochemistry 1996 41 1389-1392 Steroids and triterpenoids of Antodia cinnamomea¡ªA fungus parasitic on Cinnamomum micranthum Shu-Wei Yang, Ya-Ching Shen, Chung-Hsiung Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 31¦Â-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid C32H50O4 ÏàËÆ¶È:78.1% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 4a ÏàËÆ¶È:78.1% Journal of Natural Products 1988 Vol 51 54 Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Hypocrellol B C32H50O4 ÏàËÆ¶È:78.1% Journal of Natural Products 2011 74 2143−2150 Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524 Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . antiquol C acetate C32H50O2 ÏàËÆ¶È:75% Journal of Natural Products 2002 65 158-162 Eupha-7,9(11),24-trien-3a-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â,16¦Á-dihydroxylanosta-7,9(11),24-trien-21-oic acid ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1996 44 847-849 Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-acetoxy-¦Â-amyrin ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2006 31 131-133 Chemical constituents from roots of Ficus hirta LI Chun, BU Pengbin, YUE Dangkun, SUN Youfu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ganodermanondiol C30H48O3 ÏàËÆ¶È:75% Journal of Natural Products 1986 Vol 49 1122 Two New Lanostanoids from Ganoderma lucidum Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ganodermanondiol ÏàËÆ¶È:75% Journal of Natural Products 1988 Vol 51 54 Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ganodermanondiol C30H48O3 ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2005 36 502-504 ËÉɼÁéÖ¥µÄ»¯Ñ§³É·ÖÑо¿ ÆÕÇí»Ý,³Âºç,³ÂÈôÜ¿ Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ganoderm anondiol C30H48O3 ÏàËÆ¶È:75% Lishizhen Medicine and Materia Medica Research 2009 20 1771-1773 Chemical Constituents from Fruiting Bodies of Ganoderma lucidum. CHEN Man; ZHANG Mi; ZHANG Han-qing; SUN Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 1a C39H51NO5 ÏàËÆ¶È:74.2% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . fomitopsic acid B,21-(carboxyacetoxy)lanosta-7,9(11),24-trien-3-one C32H48O3 ÏàËÆ¶È:72.7% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . methyl 3¦Á-acetyloxylanosta-8,24-dien-21-oate ÏàËÆ¶È:72.7% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Ganoderiol A triacetate C36H56O7 ÏàËÆ¶È:72.2% Molecules 2007 12 2038-2046 Two Novel Lanostane Triterpenoids from Ganoderma Sinense Yin Qiao, Xian-min Zhang and Ming-hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . inonotsulide C C30H46O3 ÏàËÆ¶È:71.8% Helvetica Chimica Acta 2007 Vol. 90 2047 Three New Lanostane Triterpenoids from Inonotus obliquus Sayaka Taji, Takeshi Yamada, Yasuko In, Shun-ichi Wada, Yoshihide Usami, Kazuo Sakuma, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . daldinialanone C30H46O2 ÏàËÆ¶È:71.8% Journal of Natural Products 2002 65 1869-1874 Chemical Constituents of the Ascomycete Daldinia concentrica Dang Ngoc Quang, Toshihiro Hashimoto, Masami Tanaka, Manuela Baumgartner, Marc Stadler,and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 3 ÏàËÆ¶È:71.8% Journal of Natural Products 1998 61 485-487 Mediation of the Cytotoxicity of Lanostanoids and Steroids of Ganoderma tsugae through Apoptosis and Cell Cycle Kim-Hong Gan, Yih-Fen Fann, Shu-Hui Hsu, Kou-Wha Kuo, and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-Amyrin Acetate C32H52O2 ÏàËÆ¶È:71.8% Chemistry of Natural Compounds 2007 43 497-498 CHEMICAL CONSTITUENTS OF STEM BARK FROM Periploca sepium Yang-Min Ma, Qi-Hua Shi, and Yang Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ganodermanontriol C30H48O4 ÏàËÆ¶È:71.8% Journal of Chinese Pharmaceutical Sciences 1993 2 91-96 Studies on the Triterpenoid Constituents of the Spores from Ganoderma lucidum Karst Ruo-Yun Chen De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ganodermanontriol C30H48O4 ÏàËÆ¶È:71.8% Acta Pharmaceutica Sinica 1991 26 267-273 STUDIES ON THE TRITERPENOID CONSTITUENTS OF THE SPORES FROM GANODERMA LUCIDUM KARST RY Chen and DQ Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ganoderic acid SZ C30H44O3 ÏàËÆ¶È:71.8% Natural Product Research 2005 19 461-465 Ganoderic acid Sz, a new lanostanoid from the mushroom Ganoderma lucidum Canjun Li; Jianhua Yin; Fujiang Guo; Decheng Zhang; Hao H. Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 3¦Á-acetyloxylanosta-8,24-diene-21-oic acid ÏàËÆ¶È:71.8% Natural Product Research 2007 21 401-405 A new triterpenic alcohol from Fomitopsis pinicola Assya Petrova; Simeon Popov; Melania Gjosheva; Vassya Bankova Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% China Journal of Chinese Materia Medica 2008 33 405-408 Studies on phenolic compounds from Stellera chamaejasme FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% China Journal of Chinese Materia Medica 2006 31 1798-1800 Studises on chemical constituents of Balanophora spicata DAI Zhong, WANG Feng, WANG Gangli, LIN Ruichao Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 3¦Á-acetoxylanosta-8,24-dien-21-oic acid ÏàËÆ¶È:71.8% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . agnosterone, lanosta-7,9(11),24-trien-3-one ÏàËÆ¶È:71.8% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . tsugaric acid A C32H50O4 ÏàËÆ¶È:71.8% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3¦Á-hydroxy-5¦Á-lanosta-8,24-dien-21-oic acid C32H50O4 ÏàËÆ¶È:71.8% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 3-oxo-5¦Á-lanosta-8,24-dien-21-oic acid ÏàËÆ¶È:71.8% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ganodelmanontriol C30H48O4 ÏàËÆ¶È:71.8% Journal of Natural Products 1986 Vol 49 1122 Two New Lanostanoids from Ganoderma lucidum Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ganodermatriol triacetate ÏàËÆ¶È:71.8% Journal of Natural Products 1988 Vol 51 54 Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ganodermanontriol ÏàËÆ¶È:71.8% Journal of Natural Products 1988 Vol 51 54 Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 5a ÏàËÆ¶È:71.8% Journal of Natural Products 1988 Vol 51 54 Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3¦Á-acetyloxylanosta-8,24-dien-21-oic acid ÏàËÆ¶È:71.8% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Korean Journal of Pharmacognosy 2007 38(1) 76-83 Triterpenoids and Flavonoids Isolated from the Leaves of Alnus firma Yu, Young-Beob; Nakamura, Norio; Miyashiro, Hirotsugu; Hattori, Masao; Park, Jong-Cheol Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . Hypocrellol G C32H48O5 ÏàËÆ¶È:71.8% Journal of Natural Products 2011 74 2143−2150 Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524 Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . ¦Â-amyrin acetate C32H52O20 ÏàËÆ¶È:71.8% Chinese Traditional and Herbal Drugs 2008 39 182-184 Ò»Ö¦»Æ»¨»¯Ñ§³É·ÖµÄÑо¿ ѦÏþϼ;ÖÙºÆ;Ò¦ÇìÇ¿ Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . ganodermanontriol ÏàËÆ¶È:71.8% Chinese Traditional and Herbal Drugs 2007 38 1610-1612 Chemical constituents from fruiting bodies of Ganoderma tsugae (¢ò) LIU Chao; PU Qiong-hui; WANG Hong-qing; CHEN Ruo-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . ganodermanontriol ÏàËÆ¶È:71.8% Chinese Traditional and Herbal Drugs 2005 36 1601-1603 Chemical constituents from fruiting bodies of Ganoderma lucidum ZHANG Xiao-qi; YIN Zhi-qi; YE Wen-cai; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . dehydroeburiconic acid C31H48O3 ÏàËÆ¶È:71.8% Chinese Traditional and Herbal Drugs 2005 36 811-814 Chemical constituents of Fomes officinalis (¢ñ) WU Xia; YANG Jun-shan; DONG Yue-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . ¦Â-amyrin acetate C32H52O2 ÏàËÆ¶È:71.8% Chinese Journal of Natural Medicines 2007 5 31-34 Chemical Constituents of Corydalis saxicola WANG Qi-Zhi; LIANG Jing-Yu; YUAN Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Chinese Journal of Natural Medicines 2010 8 183-185 Chemical Constituents from Euphorbia ebracteolata DENG Bin; MU Shu-Zhen; HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . pulcherryl acetate ÏàËÆ¶È:71.8% Chinese Pharmaceutical Journal 2010 45 727-732 Antitumor Triterpenes from Scorzonera mongolica Maxim WANG Bin, YANG Li-ye, LI Guo-qiang, GUAN Hua-shi, TONG Guo-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Journal of Shenyang Pharmaceutical University 2006 23 10-12 Triterpenes from the fruits of Cucurbita pepo cv. Dayangua GE Shan, WANG Da-cheng, XIANG Hua, ZHU Wan-ju, DENG Xu-ming, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Journal of China Pharmaceutical University 2003 34 377-379 Stuides on the Chemical Constituents of Euphorbia ebracteolata FU Guang-Miao; YU Bo-Yang; ZHU Dan-Ni Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 24¦Á-acetoxy-3-oxoreissant-5-en-25-ol ÏàËÆ¶È:71.8% Journal of the Chemical Society, Perkin Transactions 1 1989 2259-2267 Studies on terpenoids and steroids. Part 19. Structures of three novel 19(10¡ú9)abeo-8¦Á,9¦Â,10¦Á-euphane triterpenoids from Reissantia indica(Celastraceae) Chandra B. Gamlath, A. A. Leslie Gunatilaka and Suganthini Subramaniam Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . ¦Â-amyrin acetate C32H52O2 ÏàËÆ¶È:71.8% Natural Product Research and Development 2008 20 280-282 Chemical Constituents of Twig Bank from Periploca sepium MA Yang-min;SHI Qing-hua; KONG Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Natural Product Research and Development 2006 18 74-75 Chemical Constituents of Balanophora japonica Makino RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; ZHAO Wei; WU Ji-zhou £¨ Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ¦Â-amyrin acetate C32H52O2 ÏàËÆ¶È:71.8% Natural Product Research and Development 2003 15 483-486 CHEMICAL CONSTITUENTS FROM EUPHORBIA WALLICHII WANG Huan;ZHANG Xiao-feng; PAN Li; YANG Shu-min; MA Yun-bao; LUO Xiao-dong * Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . (10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-((2R,5R,6S)-5,6,7-trihydroxy-6-methylheptan-2-yl)-4,5,6,10,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one C30H48O4 ÏàËÆ¶È:71.8% Journal of Natural Products 2011 74 2332-2337 Semisynthesis and Biological Evaluation of Ganodermanontriol and Its Stereoisomeric Triols Erin M. Kennedy, Steven J. P¡¯Pool, Jiahua Jiang, Daniel Sliva, and Robert E. Minto Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . ganodermanontriol C30H48O4 ÏàËÆ¶È:71.8% Agricultural and Biological Chemistry 1986 50 2887-2890 Ganoderiol A and B, New Triterpenoids from the Fungus Ganoderma lucidum (Reishi) Hiroji SATO, Tsuyoshi NISHITOBA, Sachiko SHIRASU, Kyoko ODA, Sadao SAKAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 3¦Â-acetoxy-17¦Â-hydroxy-28-norolean-12-ene C31H50O3 ÏàËÆ¶È:71.8% Phytotherapy Research 2008 22 1303-1306 Triterpenoids and a sterol from the stem-bark of Styrax japonica and their protein tyrosine phosphatase 1B inhibitory activities Joo-Hee Kwon, Min-Jung Chang, Hyo-Won Seo, Jeong-Hun Lee, Byung-Sun Min, MinKyun Na, Jin Cheol Kim, Mi Hee Woo, Jae Sue Choi, Hyeong Kyu Lee and KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Indian Journal of Chemistry Section B 1994 33B 302-304 Chemical constituents of Artemisia roxburghiana Bess Yu Li, Yangping Shi & Yohua Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% The Chinese Pharmaceutical Journal 2000 52 195-201 Chemical Constituents from the Leaves of Formosan Ficus septica ²ÌÑÌÁ¦(Ian-Lih Tsai), ê?ÖÇ»Ý(Jyh-Huey Chen), ¶Å²ýÒæ(Chang-Yih Duh), ê?Òæ•N(Ih-Sheng Chen) Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound 19 ÏàËÆ¶È:71.8% Journal of the American Chemical Society 1981 103 2075-2080 Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara Shujiro Seo, Yutaka Tomita, Kazuo Tori Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . ¦Á-amyrol acetate ÏàËÆ¶È:71.8% Chinese Journal of Applied & Environmental Biology 2010 16 197-201 Chemical Study on Sambucus adnata Wall CHEN Xiaozhen; LI Guoyou; WU Xiaoqing; HUANG Qingchun & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Chinese Traditional and Herbal Drugs 2012 43 1263-1266 Chemical constituents from stem barks of Daphne giraldii LIAO Shi-yu; JIANG Jian-qin Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . ¦Â-ÏãÊ÷Ö¬´¼ÒÒËáõ¥ C32H52O2 ÏàËÆ¶È:71.8% Natural Product Research and Development 2012 24 1206-1209 Chemical Constituents from Blumea megacephala ZHONG Lin-jing; LIN Xiao-yan; HUANG Ming-yu; HUANG Xiu-wang; ZHANG Yong-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . (22R)-hydroxylanosta-7,9(11),24-trien-3-one ÏàËÆ¶È:71.8% Natural Product Research 2013 27 486-490 Cytotoxic constituents from the fungus Daldinia concentrica (Xylariaceae) Dang Ngoc Quang, Duong Minh Lam, Nguyen Thi Hong Hanh & Do Duc Que Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . ¦Â-ÏãÊ÷Ö¬´¼ÒÒËáõ¥ C32H52O2 ÏàËÆ¶È:71.8% Journal of Tropical and Subtropical Botany 2009 17 160-163 Chemical Constituents of Periploca forrestii Schltr . GANG, Xiuhai, ZHOU, Xin, CHEN, Huaguo, GONG, Xiaojian, ZHANG, Jianxin, WANG, Daoping Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . ¦Â-amyrin acetate C32H52O2 ÏàËÆ¶È:71.8% Journal of Tropical and Subtropical Botany 2012 20 529-532 Chemical Constituents from Stems of Artocarpus nitidus subsp.1ingnanensis TI Hui-hui, LIU Mei-fang, LIN Li-dong, WEI Xiao-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . D:C-Frirdomadeir-7-en-3¦Â-yl acetate ÏàËÆ¶È:71.8% Helvetica Chimica Acta 1991 74 1329-1338 Madeiranes, a New Class of Pentacyclic Triterpenes: D-Friedo-madeir-14-en-3¦Â-ol and -3-one, D:C-Friedomadeir-7-en-3¦Â-ol and -3-one Maria-Jos¨¦ Umbelino Ferreira, Ana M. Lobo, Caroline A. O'Mahoney, David J. Williams and Hugo Wyler Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . ¦Â-amyrin acetate ÏàËÆ¶È:71.8% Lishizhen Medicine and Materia Medica Research 2013 24 786-787 Study on Chemical Constituents of Codonopsis thalictrifolia Wall£® var£® mollis ( Chipp) L£®T£®Shen JING Jing, ZHANG Ji-fa, LI Hui, HUANG Shuai, SHAN Lian-hai, ZHOU Xian-li* Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . compound 2 ÏàËÆ¶È:71.8% Magnetic Resonance in Chemistry 1997 35 643-646 Assignment of Carbon-13 and Proton Nuclear Magnetic Resonance Spectra of Madeirane Triterpenes Jos¨¦ R. Ascenso and Maria Jos¨¦ U. Ferreira Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . compound 5a ÏàËÆ¶È:70.5% Journal of Natural Products 1986 Vol 49 1122 Two New Lanostanoids from Ganoderma lucidum Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . compound 3a C40H53NO5 ÏàËÆ¶È:69.4% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . compound 11 ÏàËÆ¶È:69.4% Journal of the Chinese Chemical Society 1991 38 71-76 Studies on the Constituents of Ganoderma lucidum ½ªºêÕÜ(Hung-Cheh Chiang);ÖìÊÀ²ý(Shih-Chang Chu) Structure 13C NMR ̼Æ×Ä£Äâͼ |
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