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ר¼Ò¾Ñé: +726 - PhEPI: 3
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huangjiguo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-08-02 17:27:08
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huangjiguo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-08-02 17:27:08
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1¸ö ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½10384¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¦Â-hydroxytirucallic acid C30H48O3 ÏàËÆ¶È:93.3% Zeitschrift f¨¹r Naturforschung C 2003 58 505-516 Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Á-ôÇ»ù¸ÊËì-8,24-¶þÏ©-21-Ëá ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 2011 42 1293-1296 Chemical constituents from frankincense WANG, Feng, HUA, Hui-ming, WANG, Shu-mei, LIANG, Sheng-wang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxy-lanosra-8,24-dien-21-al ÏàËÆ¶È:90% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . trametenolic acid B ÏàËÆ¶È:90% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-hydroxylanosta-8,24-dien-oic acid ÏàËÆ¶È:90% Chinese Traditional and Herbal Drugs 2007 38 20-23 Chemical constituents of Stenoloma chusanum REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-ôÇ»ùÑòëçÞ-8,24-¶þÏ©-21-ôÈËá ÏàËÆ¶È:90% Chinese Journal of Medicinal Chemistry 2003 13 34-37 Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L. YANG Zhong-duo, LI Yuan-chao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . trametenolicacid ÏàËÆ¶È:90% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . trametenolic acid ÏàËÆ¶È:90% Lishizhen Medicine and Materia Medica Research 2006 17 1178-1181 Chemical Constituents of Inonotus obliquus ZHAO Fen-qin, PIAO Hui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl trametenolate ÏàËÆ¶È:87.0% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-02 10:01:05
wangkaibo123
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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huangjiguo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-08-02 17:26:58
huangjiguo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-08-02 17:26:58
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2¸ö ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½11593¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¦Â-hydroxytirucallic acid C30H48O3 ÏàËÆ¶È:96.6% Zeitschrift f¨¹r Naturforschung C 2003 58 505-516 Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Á-ôÇ»ù¸ÊËì-8,24-¶þÏ©-21-Ëá ÏàËÆ¶È:96.6% Chinese Traditional and Herbal Drugs 2011 42 1293-1296 Chemical constituents from frankincense WANG, Feng, HUA, Hui-ming, WANG, Shu-mei, LIANG, Sheng-wang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxylanosta-8,24-dien-oic acid ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 2007 38 20-23 Chemical constituents of Stenoloma chusanum REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . trametenolicacid ÏàËÆ¶È:93.3% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . trametenolic acid ÏàËÆ¶È:93.3% Lishizhen Medicine and Materia Medica Research 2006 17 1178-1181 Chemical Constituents of Inonotus obliquus ZHAO Fen-qin, PIAO Hui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl trametenolate ÏàËÆ¶È:90.3% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-hydroxy-lanosra-8,24-dien-21-al ÏàËÆ¶È:90% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . trametenolic acid B ÏàËÆ¶È:90% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-ôÇ»ùÑòëçÞ-8,24-¶þÏ©-21-ôÈËá ÏàËÆ¶È:90% Chinese Journal of Medicinal Chemistry 2003 13 34-37 Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L. YANG Zhong-duo, LI Yuan-chao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . trematenolic acid ÏàËÆ¶È:86.6% Chemical & Pharmaceutical Bulletin 2002 50(12) 1603-1606 New Triterpenoids from Tricholoma saponaceum Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . trametenolic acid ÏàËÆ¶È:86.6% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . trametenolic acid ÏàËÆ¶È:86.6% Journal of Natural Products 1999 62 543-545 New Lanostanoid Glycosides from the Fruit Body of Laetiporus versisporus Kazuko Yoshikawa, Kenji Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . trametenolic acid ÏàËÆ¶È:86.6% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . trametenolic acid B ÏàËÆ¶È:86.6% 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 15 . trametenolic acid C30H48O3 ÏàËÆ¶È:86.6% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â-dihydroxy-lanosta-8,24-diene-21-acid ÏàËÆ¶È:86.6% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . inotodiol ÏàËÆ¶È:86.6% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . trametenolicacid ÏàËÆ¶È:86.6% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 1 C31H50O3 ÏàËÆ¶È:83.8% Chinese Journal of Chemistry 2001 19 702-704 A Novel Lanostanoid Lactone From the Alga Hypnea cerricornis Xiao-Hua Xu, Xiao Chen, Jian-Hua Lu, Guang-Min Yao, Yan-Ming Li and Long-Mei Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . astrapteridiol C30H50O3 ÏàËÆ¶È:83.3% Journal of Natural Products 2008 71(12) 2077-2079 Lanostane-Type Triterpenes from the Mushroom Astraeus pteridis with Antituberculosis Activity Rita Stanikunaite, Mohamed M. Radwan, James M. Trappe, Frank Fronczek, and Samir A. Ross Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . euphol ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2005 30 1162-1165 Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity Shi Dayong, HAN Lijun, SUN Jie, YANG Yongchun, SHI Jiangong, FAN Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 15-deacetoxy-7,11-dihydroperenniporiol ÏàËÆ¶È:83.3% Phytochemistry 1984 23 2885-2888 Two perenniporiol derivatives, lanostane-type triterpenoids, from the cultured mycelia of Perenniporia ochroleuca Chieko Ino, Masao Hirotani, Tsutomu Furuya Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 3¦Â-hydroxy-lanosta-8,24-diene-21-al ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-21-dihydroxy-lanosta-8,24-diene ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Inoterpene D C30H50O3 ÏàËÆ¶È:83.3% Tetrahedron 2009 65 2443-2450 Absolute stereostructures of inoterpenes A¨CF from sclerotia of Inonotus obliquus Seikou Nakamura, Junko Iwami, Hisashi Matsuda, Shuichi Mizuno, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 21-hydroxylanosterol C30H50O2 ÏàËÆ¶È:83.3% Indian Journal of Chemistry 1987 26B 722-724 21-Hydroxylanosterol,a New Lanostane Derivative from Stem Bark of Uvariastrum zenkeri Engl. & Diels ILIAS MUHAMMAD & CHOUDHUPY M HASAN Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 2a C39H53NO5 ÏàËÆ¶È:82.8% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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