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²éѯ½á¹û£º¹²²éµ½475¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ganoderiol B C30H48O2 ÏàËÆ¶È:93.5% 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 2 . ganoderiol B C30H48O2 ÏàËÆ¶È:93.5% 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 3 . ganodermadiol C30H48O2 ÏàËÆ¶È:93.5% Journal of Natural Products 1986 Vol 49 621 Three New Lanostanoids from Ganoderma lucidum Munehisa Arisawa, Akio Fujita, Manabu Saga, Hideki Fukumura, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ganodermadiol ÏàËÆ¶È:93.5% 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 5 . 5¦Á-lanosta-7,9(11),24-trien-3¦Â,26-diol ÏàËÆ¶È:93.5% 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 6 . Ganoderiol B ÏàËÆ¶È:93.5% Lishizhen Medicine and Materia Medica Research 2008 19 2776-2777 Studies on the Chemical Constituents and Cytotoxicity from the Fruiting Body of Ganoderma lucidum MAN Su-li; GAO Wen-yuan; YAN Lu-lu; ZHANG Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ganoderiol B C30H48O2 ÏàËÆ¶È:93.5% 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 8 . Ganodermadiol ÏàËÆ¶È:93.5% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ganoderiol B C30H48O2 ÏàËÆ¶È:93.5% Mycosystema 2015 34 124−130 Compounds from the fruiting bodies of Phellinus baumii and their inhibition to tumor cell proliferation FENG Na WU Na, YANG Yan ZHANG Jing-Song TANG Qing-Jiu SHAO Qian Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â, 21-dihydroxylanosta- 7,9(11)-diene ÏàËÆ¶È:83.8% 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 11 . lucidumol B ÏàËÆ¶È:83.8% 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 12 . 23-Hydroxyganoderic Acid S C30H48O5 ÏàËÆ¶È:83.8% Journal of Natural Products 2010 73 897-900 Antiplasmodial Lanostanes from the Ganoderma lucidum Mushroom Michael Adams, Marco Christen, Inken Plitzko, Stefanie Zimmermann, Reto Brun, Marcel Kaiser and Matthias Hamburger Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound I ÏàËÆ¶È:83.8% 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 14 . ganodermatriol ÏàËÆ¶È:83.8% 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 15 . ganoderiol C30H50O4 ÏàËÆ¶È:83.8% 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 16 . ganodermatriol C30H48O3 ÏàËÆ¶È:83.8% 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 17 . ¦Ã-lanostadienol ÏàËÆ¶È:83.8% Organic Magnetic Resonance 1974 6 603-611 Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids S. A. Knight Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . dihydroagnosterol ÏàËÆ¶È:83.8% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Lucidumol B ÏàËÆ¶È:83.8% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ganoderiol A ÏàËÆ¶È:83.8% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ganoderiol A C30H50O4 ÏàËÆ¶È:80.6% 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 22 . ganoderiol A C30H50O4 ÏàËÆ¶È:80.6% 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 23 . Ganodermatriol ÏàËÆ¶È:80.6% Journal of Natural Medicines 2009 63 304-310 Metabolism and pharmacokinetics in rats of ganoderiol F, a highly cytotoxic and antitumor triterpene from Ganoderma lucidum Qun Zhang, Feng Zuo, Norio Nakamura, Chao-Mei Ma and Masao Hattori Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ganoderiol A ÏàËÆ¶È:80.6% 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 25 . epoxyganoderiol C C30H48O3 ÏàËÆ¶È:80.6% Agricultural and Biological Chemistry 1988 52 211-216 Novel Triterpenoids and a Steroid from the Fungus Ganoderma lucidum Tsuyoshi NISHITOBA, Hiroji SATO, Kyoko ODA, Sadao SAKAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . agnosterol ÏàËÆ¶È:80.6% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Epoxyganoderiol C ÏàËÆ¶È:80.6% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . inonotsutriol C C30H48O3 ÏàËÆ¶È:77.4% 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 29 . lucialdehyde A C30H46O2 ÏàËÆ¶È:77.4% 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 30 . 5¦Á-lanosta-7,9(11),24-triene-3¦Â-hydroxy-26-al C30H46O2 ÏàËÆ¶È:77.4% 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 31 . 3¦Â,22-dihydroxylanosta-7,9(11),24-triene ÏàËÆ¶È:77.4% 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 32 . ganodermatriol C30H48O3 ÏàËÆ¶È:77.4% 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 33 . ganodermatriol C30H48O3 ÏàËÆ¶È:77.4% 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 34 . 24-methylenelanosta-7,9(11)dien-3¦Â-ol ÏàËÆ¶È:77.4% Phytochemistry 1998 49 2053-2056 24-methylene tetracyclic triterpenes from Polyalthia lancilimba Y. P. Lue, Q. Mu, H. L. Zheng, C. M. Li Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 24-methylene-lanosta-7,9(11)dien-3¦Â-ol C31H50O ÏàËÆ¶È:77.4% Journal of Natural Products 1987 Vol 50 762 Chemistry in the Annonaceae, XXIII. 24-Methylene-lanosta-7,9(11)-dien-3¦Â-ol from Artabotrys odorotissimus Stem Bark Choudhury M. Hasan, Shaheen Shahnaz, Ilias Muhammad, Alexander I. Gray, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 20 ÏàËÆ¶È:77.4% Magnetic Resonance in Chemistry 1989 27 258-262 Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives Jacek Martynow and Zdzisław Paryzek Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound 20 ÏàËÆ¶È:77.4% Magnetic Resonance in Chemistry 1989 27 258-262 Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives Jacek Martynow and Zdzisław Paryzek Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 5¦Á-Lanosta-7,9(11),24-triene-3¦Â-hydroxy-26-al ÏàËÆ¶È:77.4% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . Lucialdehyde A ÏàËÆ¶È:77.4% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . Lanosta-7,9(11)-dien-3¦Â-acetyloxy-24,26-dihydroxy-25-methoxy C33H54O5 ÏàËÆ¶È:75.7% Phytochemistry 2015 110 133−139 Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 24Z-ethylidenelanost-8-en-3¦Â-ol C31H54O ÏàËÆ¶È:75% Phytochemistry 1994 37 201-203 Lanostane triterpenes from the bark of Neolitsea sericea Mahesh C. Sharma, Tatsuro Ohira, Mitsuyoshi Yatagai Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . Lanosta-7,9(11)-dien-3¦Â-acetyloxy-24,25,26-trihydroxy C32H52O5 ÏàËÆ¶È:75% Phytochemistry 2015 110 133−139 Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 3¦Â,22-dihydroxylanosta-7,9(11), 24- triene C30H48O2 ÏàËÆ¶È:74.1% 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 44 . lanosta-7,9(11),24-trien-3¦Â,21-diol ÏàËÆ¶È:74.1% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . ganodermenonol C30H46O2 ÏàËÆ¶È:74.1% Journal of Natural Products 1986 Vol 49 621 Three New Lanostanoids from Ganoderma lucidum Munehisa Arisawa, Akio Fujita, Manabu Saga, Hideki Fukumura, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . ganodermenonol ÏàËÆ¶È:74.1% 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 47 . lanost-8(9)-en-3¦Â-ol ÏàËÆ¶È:74.1% Canadian Journal of Chemistry 1977 55 2813-2828 The semiempirical derivation of 13C nuclear magnetic resonance chemical shifts. Hydrocarbons, alcohols, amines, ketones, and olefins Helmut Beierbeck, John K. Saunders, John W. Apsimon Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . ganodercochlearin C C31H50O3 ÏàËÆ¶È:74.1% Journal of Natural Products 2014 77 737-743 Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear Xing-Rong Peng, Jie-Qing Liu, Cui-Fang Wang, Xu-Yang Li, Yi Shu, Lin Zhou, and Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 3¦Â-hydroxy-5¦Á-lanost-8-ene ÏàËÆ¶È:74.1% Magnetic Resonance in Chemistry 1989 27 258-262 Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives Jacek Martynow and Zdzisław Paryzek Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . dihydrolanosterol ÏàËÆ¶È:74.1% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . compound 1 ÏàËÆ¶È:74.1% Magnetic Resonance in Chemistry 1989 27 258-262 Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives Jacek Martynow and Zdzisław Paryzek Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . Ganodermenonol ÏàËÆ¶È:74.1% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . (24E)-24-ethyl-29-nor-5¦Á-lanosta-7,9(11),24(241)-trien-3¦Â-yl acetate C26H38O2 ÏàËÆ¶È:71.8% Chemical & Pharmaceutical Bulletin 1996 44 1202-1207 Eight Novel Sterols from the Roots of Bryonia dioica JACQ. Toshihiro AKIHISA,Yumiko KIMURA,Wilhelmus C. M. C. KOKKE,Takashi ITOH and Toshitake TAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . Lanosta-7,9(11),24E-trien-3¦Â-acetyloxy-26,27-dihydroxy C32H50O4 ÏàËÆ¶È:71.8% Phytochemistry 2015 110 133−139 Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . compound 9b ÏàËÆ¶È:71.8% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. 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Inoterpene A C30H52O3 ÏàËÆ¶È:67.7% 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 118 . Inoterpene B C30H52O3 ÏàËÆ¶È:67.7% 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 119 . 22,23;24,25-diepoxy-3¦Â-hydroxy-7-tirucallene C30H48O3 ÏàËÆ¶È:67.7% Planta Medica 2011 77 1844-1847 Cytotoxic Triterpenoids from Azadirachta indica Chen, JinXiong; Chen, JianChao; Sun, Yun; Yan, YuXin; Kong, LingMei; Li, Yan; Qiu, MingHua: Structure 13C NMR ̼Æ×Ä£Äâͼ 120 . (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:67.7% |

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