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ÕÅÁÖÑÒľ³æ (СÓÐÃûÆø)
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13C-NMR ZX03 12.5,15.6,15.8,18.0,22.7,23.0,25.7,26.0,27.0,27.8,28.2,29.2,31.7,35.7,37.4, 37.8,38.7,41.5,44.2,47.8,49.2,49.9,73.4,79.0,116.2,120.5,121.3,135.2,142.5, 146.0 |
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Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
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ÕÅÁÖÑÒ(jiangchunyong´ú·¢): ½ð±Ò+20, лл 2013-04-28 20:48:15
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ÕÅÁÖÑÒ(jiangchunyong´ú·¢): ½ð±Ò+20, лл 2013-04-28 20:48:15
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1 . 3¦Â,22-dihydroxylanosta-7,9(11),24-triene ÏàËÆ¶È:100% 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 2 . 3¦Â ,22-dihydroxylanosta-7,9(11), 24- triene C30H48O2 ÏàËÆ¶È:100% Planta Medica 1986 52 495-496 3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus Kirsti Kahlos and R. Hiltunen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . daldinialanone C30H46O2 ÏàËÆ¶È:86.6% 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 4 . lanosta-7:9(11),23E-triene-3¦Â,22R,25-triol C30H48O3 ÏàËÆ¶È:86.6% European Journal of Medicinal Chemistry 2008 43 2373-2379 Lanostane-type triterpenoids from the sclerotia of Inonotus obliquus possessing anti-tumor promoting activity Sayaka Taji, Takeshi Yamada, Shun-ichi Wada, Harukuni Tokuda, Kazuo Sakuma, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (22R)-hydroxylanosta-7,9(11),24-trien-3-one ÏàËÆ¶È:86.6% 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 6 . lucidumol B ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1998 46 1607-1612 Triterpenes from the Spores of Ganoderma lucidum and Their Inhibitory Activity against HIV-1 Protease Byung-Sun MIN,Norio NAKAMURA,Hirotsugu MIYASHIRO,Ki-Whan BAE and Masao HATTORI Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-hydroxylanosta-7,9(11),24-trien-21-oic acid C30H46O3 ÏàËÆ¶È:83.3% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Hypocrellol A C30H48O3 ÏàËÆ¶È:83.3% 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 9 . ganoderiol A C30H50O4 ÏàËÆ¶È:80% Journal of Chinese Pharmaceutical Sciences 1997 6 291-791 Triterpenoids from the Fruiting Body of Ganoderma lucidum Fang-Sheng Wang, Hui Cai, Jun-Shan Yang, Yu-Mei Zhang and Ying-Ju Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ganoderiol A C30H50O4 ÏàËÆ¶È:80% Acta Pharmaceutica Sinica 1996 31 200-204 STUDIES ON THE TRITERPENOID CONSTITUENTS FROM THE FRUITING BODY OF GANODERMA LUCIDUM (FR.)KARST. FS Wang; H Cai; JS Yang; YM Zhang and YJ Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . lanosta-7,9(11),24-trien-3¦Â,21-diol ÏàËÆ¶È:80% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-alcohol ÏàËÆ¶È:80% 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 13 . ganodermadiol ÏàËÆ¶È:80% 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 14 . 3¦Â-ol of ganodermanondiol ÏàËÆ¶È:80% 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 15 . ganoderiol A ÏàËÆ¶È:80% 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 16 . Methoxyinonotsutriol C31H52O4 ÏàËÆ¶È:77.4% Phytochemistry Letters 2012 5 480-485 Four new lanostane-type triterpenoids from Inonotus obliquus Noriko Handa, Takeshi Yamada, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . inonotsutriol C C30H48O3 ÏàËÆ¶È:76.6% Helvetica Chimica Acta 2008 Vol. 91 1513 Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus Sayaka Taji, Takeshi Yamada, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . lucialdehyde A C30H46O2 ÏàËÆ¶È:76.6% Chemical & Pharmaceutical Bulletin 2002 50(6) 837-840 New Triterpene Aldehydes, Lucialdehydes A¡ªC, from Ganoderma lucidum and Their Cytotoxicity against Murine and Human Tumor Cells Jiang-Jing GAO,Byung-Sun MIN,Eun-Mi AHN,Norio NAKAMURA,Hyeong-Kyu LEE,and Masao HATTORI Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 5¦Á-lanosta-7,9(11),24-triene-3¦Â-hydroxy-26-al C30H46O2 ÏàËÆ¶È:76.6% Journal of Natural Products 2002 65 417-421 New Lanostanoids from the Fungus Ganoderma concinna Antonio G. Gonz¨¢lez,Francisco Le¨®n, Augusto Rivera, Juan I. Padr¨®n, Javier Gonz¨¢lez-Plata,Juan C. Zuluaga,Jos¨¦ Quintana, Francisco Est¨¦vez, and Jaime Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â, 21-dihydroxylanosta- 7,9(11)-diene ÏàËÆ¶È:76.6% Planta Medica 1986 52 495-496 3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus Kirsti Kahlos and R. Hiltunen Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . inotodiol ÏàËÆ¶È:76.6% Planta Medica 1986 52 495-496 3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus Kirsti Kahlos and R. Hiltunen Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-28 15:17:46
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