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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£º¹²²éµ½9672¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol 2¦Â,3¦Á-diacetate ÏàËÆ¶È:75% Journal of Natural Products 1991 Vol 54 998 Novel Cytotoxic Principles of Formosan Ganoderma lucidum Chun-Nan Lin, Whey-Pim Tome, Shen-Jeu Won Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol 2¦Â,3¦Á-diacetate ÏàËÆ¶È:75% Phytochemistry 1993 32 1549-1551 Steroids of formosan Ganoderma amboinense Lin Chun-Nan, Kuo Shih-Hsieh, Won Shen-Jeu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene C30H52O3 ÏàËÆ¶È:75% Zeitschrift f¨¹r Naturforschung C 2002 57 489-495 Microbial Transformation of a Mixture of Argentatin A and Incanilin Key words: Argentatin A, Incanilin, Biotransformation Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:75% Natural Product Communications 2009 4 1449-1454 Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp. Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:75% Natural Product Communications 2009 4 1449-1454 Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp. Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ergosteryl myristate C42H70O2 ÏàËÆ¶È:73.5% Natural Product Sciences 1999 5 93-96 Ergosteryl Myristate, a New Ergosterol Derivative from Unidentified Marine Algicolous Fungus Lee, Dong-Ick; Choi, Jin-Souk; Yang, Mi-Rim; Lee, Won-Kap; Kim, Dong-Soo; Choi, Hong-Dae; Son, Byeng-Wha Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,5¦Á,6¦Á-Trihydroxyergosta-7,22-diene 6-O-benzoate C35H50O4 ÏàËÆ¶È:72.7% Journal of Natural Medicines 2011 65 307-312 Constituents of cultivated Agaricus blazei Yumi Ueguchi ,Katsuyoshi Matsunami ,Hideaki Otsuka ,Kazunari Kondo Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Globosterol C29H47O3 ÏàËÆ¶È:71.8% Steroids 2009 74 786-790 Polyhydroxylated steroids from an endophytic fungus, Chaetomium globosum ZY-22 isolated from Ginkgo biloba Jian-Chun Qin, Jin-Ming Gao, Ya-Mei Zhang, Sheng-Xiang Yang, Ming-Sheng Bai, Ya-Tuan Ma, Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ergosta-7,22-dien-3¦Â-ylpentadecanoate 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 10 . 24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:71.8% Bulletin of the Korean Chemical Society 2011 32 697-700 Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . methylsirosterol C48H63O7 ÏàËÆ¶È:71.8% Canadian Journal of Chemistry 1992 70 1905-1913 Sirosterol and dehydroazasirosterol, unusual steroidal adducts from a Sirococcus species William A. Ayer, Yu-Ting Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (22E,24R)-3,6-Diacetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:71.8% Natural Product Communications 2009 4 1449-1454 Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp. Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ergosta-7,22-diene-3¦Â-yl pentadecanoate ÏàËÆ¶È:71.8% Journal of Chinese Medicinal Materials 2008 31 41-44 Chemical Constituents of the Spores of Ganoderma lucidum ZHANG Xiao-qi, PANG Guo-liang, CHENG Yan, WANG Ying, YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (22E)-6 -Methoxy-3 ¦Á,5-cyclo-24 -methyl-5 ¦Á-cholest-22-ene C29H48O ÏàËÆ¶È:68.7% Steroids 2002 67 597-603 [3,3]-Claisen rearrangements in 24¦Á-methyl steroid synthesis: Application to campesterol, crinosterol, and ¦¤25-crinosterol side chain construction Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Andrey P. Antonchick, Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (24R,241R)-24(241)-epoxyisoavenasteryl acetate ÏàËÆ¶È:68.7% Phytochemistry 1999 52 1601-1605 (24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica Toshihiro Akihisa, Yumiko Kimura, Kazuo Koike, Wilhelmus C.M.C. Kokke, Tadashi Ohkawa, Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ |

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