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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£º¹²²éµ½10186¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (4S,10R,9S,13R,14S)-14,13,27-trimethyl-1[(20R,24S)-20,24,25-trimethyl-25-heptyl]perhydrocyclopenta[a]cyclopropa[e]phenanthren-3-one] C30H48O ÏàËÆ¶È:96.6% Chemistry of Natural Compounds 2012 48 816-820 Ozonolysis of cyclomusalenone and its derivatives I. E. Smirnova, H. Do Thi Thu, O. B. Kazakova, G. A. Tolstikov, A. N. Lobov, K. Yu. Suponitskii Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-epicyclomusalenol ÏàËÆ¶È:86.6% China Journal of Chinese Materia Medica 2009 34 2607-2609 Triterpenes from Corallodiscus kingianus KANGWenyi, CHEN Lin, ZANG Xinyan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cyclolaudenol ÏàËÆ¶È:83.8% Journal of Natural Products 2001 64 953-955 Triterpenoids from Tillandsia fasciculata Zulema Cantillo-Ciau,Wendy Brito-Loeza,and Leovigildo Quijano Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Cyclolaudenol ÏàËÆ¶È:83.8% Molecules 2008 13 255-266 New Benzoyl Glucosides and Cytotoxic Pterosin Sesquiterpenes from Pteris ensiformis Burm. Yung-Husan Chen, Fang-Rong Chang, Mei-Chin Lu, Pei-Wen Hsieh, Ming-Jiuan Wu, Ying-Chi Du and Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-epi-cycloaudenol C31H52O ÏàËÆ¶È:83.8% Indian Journal of Chemistry 1996 35B 1113-1115 occurrence of 24-alkyl-9¦Â,19-cyclolanost-25-enes in Murraya exotica L. E K Desoky Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (24S)-24-Methyl-29-nor-cycloart-25-en-3-methoxyoxime [(4S,10R,9S,13R,14S)-14,13,27-trimethyl-1[(20R,24S)-20,24,25-trimethyl-25-heptyl]perhydrocyclopenta[a]cyclopropa[e]phenanthren-3-methoximino-25-ene] C31H51NO ÏàËÆ¶È:83.8% Chemistry of Natural Compounds 2012 48 816-820 Ozonolysis of cyclomusalenone and its derivatives I. E. Smirnova, H. Do Thi Thu, O. B. Kazakova, G. A. Tolstikov, A. N. Lobov, K. Yu. Suponitskii Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 24-methyl-9,19-cyclolanost-25-en-3-ol ÏàËÆ¶È:83.8% Chinese Traditional and Herbal Drugs 2013 44 812-815 Study on chemical constituents of Aletris spicata HUANG Lan, PAN Jie, CAO Pei-xue, PAN Wei-dong, LIANG Guang-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-epicyclomusalenone C29H45O ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1997 45 744-746 4-Epicycloeucalenone and 4-Epicyclomusalenone : Two 3-Oxo-28-norcycloartanes from the Fruit Peel of Musa sapientum L. Toshihiro AKIHISA,Yumiko KIMURA,Wilhelmus C. M. C. KOKKE,Sei-ichi TAKASE,Ken YASUKAWA,Aiko JIN-NAI and Toshitake TAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-epicyclomusalenol C30H50O ÏàËÆ¶È:83.3% Phytochemistry 1998 47 1107-1110 Cycloartane triterpenes from the fruit peel of Musa sapientum Toshihiro Akihisa, Yumiko Kimura, Toshitake Tamura Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (24R)-cycloartane-3¦Â,24,25,28-tetrol C30H52O4 ÏàËÆ¶È:83.3% Phytochemistry 1997 46 397-381 Cycloartane triterpenoids from Aglaia harmsiana Akira Inada, Shintaro Ohtsuki, Takako Sorano, Hiroko Murata, Yuka Inatomi, Dedy Darnaedi, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (24S)-24-Methyl-29-nor-cycloart-25-en-3-oxime [(4S,10R,9S,13R,14S)-14,13,27-trimethyl-1[(20R,24S)-20,24,25-trimethyl-25-heptyl]perhydrocyclopenta[a]cyclopropa[e]phenanthren-3-oximino-25-ene] C30H49NO ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 2012 48 816-820 Ozonolysis of cyclomusalenone and its derivatives I. E. Smirnova, H. Do Thi Thu, O. B. Kazakova, G. A. Tolstikov, A. N. Lobov, K. Yu. Suponitskii Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 28-norcycloartan-24(31)-en-3-one ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2012 43 636-639 Chemical constituents in roots of Pandanus tectorius LIU Jia-wei; PENG Li-hua; XIAN Mei-ting; CHENG Jin-le; CHEN Wei-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cyclolaudenyl acetate ÏàËÆ¶È:80.6% Journal of Natural Products 2001 64 953-955 Triterpenoids from Tillandsia fasciculata Zulema Cantillo-Ciau,Wendy Brito-Loeza,and Leovigildo Quijano Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Sinocalycanchinensin G C29H44O3 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2011 19 2790-2796 New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis Yoshiki Kashiwada , Kazuya Nishimura, Shin-ichiro Kurimoto, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Sinocalycanchinensin H C32H50O6 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2011 19 2790-2796 New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis Yoshiki Kashiwada , Kazuya Nishimura, Shin-ichiro Kurimoto, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . cycloeucalenone ÏàËÆ¶È:80% Phytochemistry 1978 17 1975-1978 A new triterpene glucoside from Cymbidium giganteum Jan Dahm¨¦n, Kurt Leander Structure 13C NMR ̼Æ×Ä£Äâͼ |

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