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²éѯ½á¹û£º¹²²éµ½29216¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (3¦Â,5¦Á,6¦Â,22E)-6-methoxyergosta-7,22-diene-3,5-diol ÏàËÆ¶È:100% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene C29H48O3 ÏàËÆ¶È:100% Phytochemistry 1988 27 2777-2779 Cytotoxic steroids from the mushroom Agaricus blazei Hirokazu Kawagishi,Ryosuke Katsumi,Toshimi Sazawa,Takashi Mizuno,Toshihiko Hagiwara,Takuji Nakamura Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â,5¦Á-Dihydroxy-6¦Â-methoxyergosta-7,22-diene ÏàËÆ¶È:100% Archives of Pharmacal Research 2002 25 851-855 Cytotoxic ergosterols from paecilomyces sp. J300 Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene ÏàËÆ¶È:100% Archives of Pharmacal Research 2006 29 548-555 Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata Ik Soo Lee, Wen Yi Jin, Xinfeng Zhang, Tran Manh Hung and Kyung Sik Song, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 22E-6¦Â-methoxyergosta-7,22-diene-3¦Â,5¦Á-diol C29H48O3 ÏàËÆ¶È:100% Journal of Shenyang Pharmaceutical University 2012 29 678-684 A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1) LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6-methoxy-cerevisterol ÏàËÆ¶È:96.5% Natural Product Research and Development 2007 19 605-609 Study on the Chemical Constitutes of Hydnellum concrescens YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (22E,24R)-6¦Â-¼×Ñõ»ùÂó½ÇçÞ-7,22-¶þÏ©-3¦Â,5¦Á-¶þ´¼ ÏàËÆ¶È:96.5% Journal of Chinese Medicinal Materials 2008 31 1343-1347 Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21 GAO Zong-hua, MA Li-ying, SHEN Yun-xiu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3¦Â,5¦Á,6¦Â,22E)-Âó½ÇçÞ-7,22-¶þÏ©-3,5,6-Èý´¼ C28H46O3 ÏàËÆ¶È:93.1% Chinese Journal of Antibiotics 2011 36 576-580 Antibacterial metabolites from the endophytic fungus R7 of Aquilaria sinensis Wei, Jing, Dai, Hao-Fu, Yu, Lei, Wang, Hui, and, Mei, Wen-Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . fomentarol C C30H50O3 ÏàËÆ¶È:90% Phytochemistry 2013 92 137-145 Fomentarols A¨CD, sterols from the polypore macrofungus Fomes fomentarius Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene C30H50O3 ÏàËÆ¶È:90% Tetrahedron Letters 2013 54 4900-4902 An unusual sterol from the mushroom Stropharia rugosoannulata Jing Wu, Tomohiro Suzuki, Jae-Hoon Choi, Nobuhiro Yasuda, Keiichi Noguchi, Hirofumi Hirai, Hirokazu Kawagishi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:90% 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 12 . (5 ¦Á,6¦Â,15¦Â,22E)-6-ethoxy-5,15-dihydroxyergosta-7,22-dien-3-one C30H48O4 ÏàËÆ¶È:90% Chemistry & Biodiversity 2013 10 1276-1283 Two New Steroids from an Endophytic Fungus Phomopsis sp. Shao-Hua Wu, Rong Huang, Cui-Ping Miao and You-Wei Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cerevisterol ÏàËÆ¶È:89.6% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6,9-epoxyergosta-7,22-dien-3-ol ÏàËÆ¶È:89.6% Acta Botanica Sinica 2002 44 1239-1242 Chemical Constituents of One Species of Endophytic Fungus in Taxus chinensis ZHANGJi-Hui, GUO Shun-Xing YANGJun-Shan, XIAO Pei-Gen Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol,respectively C28H46O3 ÏàËÆ¶È:89.6% Chinese Chemical Letters 2006 17 481-484 An Abietane Diterpene and a Sterol from Fungus Phellinus igniarius Ying WANG, Su Juan WANG, Shun Yan MO, Shuai LI, Yong Chun YANG, Jian Gong SHI Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:89.6% Biochemical Systematics and Ecology 2007 35 790-793 Triterpenes and steroids from Armillaria mellea Vahl. ex Fr. Wen-Juan Guo, Shun-Xing Guo, Jun-Shan Yang, Xiao-Mei Chen, Pei-Gen Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol C28H44O2 ÏàËÆ¶È:89.6% Phytochemistry 1999 51 891-898 Antitumor sterols from the mycelia of Cordyceps sinensis Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . cerevisterol ÏàËÆ¶È:89.6% Phytochemistry 1997 44 1443-1448 Cytochalasins and phytotoxins from the fungus Xylaria obovata Dawit Abate, Wolf-Rainer Abraham, Holger Meyer Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 5¦Á-ergosta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:89.6% Journal of Natural Products 1988 Vol 51 1098 Polar Steroids from the Marine Scallop Patinopecten yessoensis Maria Iorizzi, Luigi Minale, Raffaele Riccio, Jong-Soo Lee, Takeshi Yasumoto Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol C28H46O3 ÏàËÆ¶È:89.6% 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 |
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