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1 . (3¦Â,5¦Á,6¦Â,22E)-6-methoxyergosta-7,22-diene-3,5-diol ÏàËÆ¶È:90% 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:90% 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 . 6-methoxy-cerevisterol ÏàËÆ¶È:90% 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 4 . 22E-6¦Â-methoxyergosta-7,22-diene-3¦Â,5¦Á-diol C29H48O3 ÏàËÆ¶È:90% 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 5 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol C28H44O2 ÏàËÆ¶È:86.6% 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 6 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol C28H46O3 ÏàËÆ¶È:86.6% 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 7 . 5,6-Epoxy-22-en-3-ol-ergosterol C28H44O2 ÏàËÆ¶È:86.6% Chemical Research in Chinese Universities 1998 14 270-272 Chemical Constituent of Natural Body of Armillaria mellea and Structure of 5, 6-Epoxy-22-en-3-ol-ergosterol SHI Lei, CAO Rui-min, LU Shi-xiang and WU Guang-xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . cerevisterol (3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene) ÏàËÆ¶È:86.6% 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 9 . ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol ÏàËÆ¶È:86.6% Chinese Traditional and Herbal Drugs 2000 31 328-330 ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿ Íò»Ô Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â,5¦Á-Dihydroxy-6¦Â-methoxyergosta-7,22-diene ÏàËÆ¶È:86.6% 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 11 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol ÏàËÆ¶È:86.6% Chinese Journal of Medicinal Chemistry 2008 18 452-456 Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol ÏàËÆ¶È:86.6% Natural Product Research and Development 1999 11(6) 18-21 THREE STEROLS FROM GYROPORUS CASTANEUS Wan Hui; Sun Rongqi; Wu Dajun; Guo Beishu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol ÏàËÆ¶È:86.6% Phytotherapy Research 2011 25 1579-1585 Ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol from the Fruit Bodies of Ganoderma lucidum Induces Apoptosis in Human Myelocytic HL-60 Cells Mi Kyoung Lee, Tran Manh Hung, To Dao Cuong, MinKyun Na, Jin Cheol Kim, Eun-Jung Kim, Hee-Sung Park, Jae Sue Choi, IkSoo Lee, KiHwan Bae, Masao Hattori and Byung Sun Min Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cerevisterol ÏàËÆ¶È:86.6% Mycosystema 2010 29 249-253 Steroids from fruiting bodies of Coprinus comatus and their inhibition to tumor cell proliferation FENG Na; ZHANG Jing-Song TANG Qing-Jiu HAO Rui-Xia LIU Yan-Fang YANG Yan JIA Wei ZHOU Shuai TANG Chuan-Hong ZHONG Jian-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . cerevisterol ÏàËÆ¶È:83.3% 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 16 . 6,9-epoxyergosta-7,22-dien-3-ol ÏàËÆ¶È:83.3% 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 17 . 6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:83.3% 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 18 . cerevisterol ÏàËÆ¶È:83.3% 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 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Chinese Journal of Medicinal Chemistry 2005 15 221-223 The chemical constituents from the mycel ia of marine fungus Rhizopus sp. SHI Ying, TIAN Li, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Natural Product Research and Development 2006 18 238-242 Chemical Study on Porandra scandens HE Zhi-heng; LUO Ying-gang; LI Hong-juan£¨; ZHANG Guo-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Natural Product Research and Development 2006 18 411-414 Phytochemical Study on Zehneria maysorensis LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Á-triol C28H46O3 ÏàËÆ¶È:83.3% Natural product sciences 2011 17 85-89 Cytotoxicity of Ergosterol Derivatives from the Fruiting Bodies of Hygrophorus russula Lee, Ik-Soo; Kim, Jin-Pyo; Na, Min-Kyun; Jung, Hyun-Ju; Min, Byung-Sun; Bae, Ki-Hwan Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2011 42 31-33 Chemical constituents of Dendrobium crystallinum WANG Lei, ZHANG Chao-feng, WANG Zheng-tao, ZHANG Mian, XU Luo-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (22E,24R)-ergosta-7,22-dien-2¦Á,3¦Á,9¦Á-triol C28H46O3 ÏàËÆ¶È:83.3% The Journal of Antibiotics 2012 65 437-440 Inhibition of human neutrophil elastase by ergosterol derivatives from the mycelium of Phellinus linteus Ik-Soo Lee, KiHwan Bae, Jae Kuk Yoo, In-Ja Ryoo, Bo Yeon Kim, Jong Seog Ahn and Ick-Dong Yoo Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C28H44O2 ÏàËÆ¶È:83.3% Natural Medicines 1996 50 179-181 Sterol Constituents from the Sclerotium of Polyporus umbellatus Fries OHTA KOJI,YAOITA YASUNORI,MATSUDA NORIKO Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (22E)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Chinese Journal of Marine Drugs 2012 31 5-10 Studies on chemical constituents of the South China Sea Gorgonian Rumphella aggregata LIU Cai-xia; LI Ping-lin; TANG Xu-li; LI Guo-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2012 43 664-666 Studies on chemical constituents of Lasiosphaera fenzlii SU Ming-zhi; LUO Zhou; YAN Ming; ZHAO Qing-chun Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 22E-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:83.3% 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 29 . stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol,respectively C28H46O3 ÏàËÆ¶È:80% 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 30 . biemnasterol C28H44O3 ÏàËÆ¶È:80% Journal of Natural Products 1993 Vol 56 2016 Biemnasterol, a New Cytotoxic Sterol with the Rare 22,25-Diene Side Chain, Isolated from the Marine Sponge Biemna sp. Chun-min Zeng, Masami Ishibashi, Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 6,9-epoxy-ergosta-7,22-dien-3-ol C28H44O2 ÏàËÆ¶È:80% Acta Pharmaceutica Sinica 2000 Vol 35 367-369 THE STEROL CONSTITUENTS OF MYCENA DENDROBII CHEN Xiao Mei; YANG Jun Shan; GUO Shun Xing Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 9(11)-dehydroergosterol peroxide C28H44O3 ÏàËÆ¶È:80% Natural Product Sciences 2009 15 173-179 Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2008 39 1776-1778 Chemical constituents of Russula virescens TANG Jian-guo; SHAO Hong-jun; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 8,9-epoxyergosta-5,22-dien-3¦Â,15-diol C28H44O3 ÏàËÆ¶È:80% 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 35 . 3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene C30H52O3 ÏàËÆ¶È:80% 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 36 . (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:80% 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 37 . (22E,24R)-3¦Â,5¦Á,6¦Á-trihydroxyergosta-7,22-diene ÏàËÆ¶È:80% 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 38 . Ergosta-7,22-dien-3¦Â,5¦Á,6¦Á-triol C28H46O3 ÏàËÆ¶È:80% Journal of Anhui Agricultural Sciences 2010 38 2356-2357 Research on the Chemical Componen ts of the Fruit Bodies ofBoletus calopus ZUOW ei et al Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 24-methyl-7¦Á,8¦Á-epoxy-3¦Â,5¦Á,6¦Á-trihydroxycholest-22-ene C28H46O4 ÏàËÆ¶È:76.6% Journal of Natural Products 1996 59 679-682 Isolation of Polyhydroxysteroids from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo, Jung-Rae Rho, and Ki Woong Cho Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . cerevisterol C28H46O3 ÏàËÆ¶È:76.6% Acta Botanica Yunnanica 2006 28(3) 315-318 A New Steroidal Glycoside from the Fruiting Bodies of Tylopilus virens (Boletaceae) WANG Fei,ZHANGLing, DONG Ze-Jun,LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 3¦Â-acteoxy-(22E, 24R)-24-methyl-5¦Á-cholest-7, 22-diene-5, 6¦Â-diol C30H48O4 ÏàËÆ¶È:76.6% Acta Botanica Yunnanica 2002 24(4) 125-128 The Chemical Constituents from Basidiocarps of Sarcodon aspratum HUANG Yue,DONG Ze-Jun,LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:76.6% Chemistry of Natural Compounds 2009 45 124-125 COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus Weiwei Zhou, Shunxing Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol) ÏàËÆ¶È:76.6% Steroids 2001 66 771-775 A novel sterol from Chinese truffles Tuber indicum Gao Jinming, Hu Lin, Liu Jikai Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Globosterol C29H47O3 ÏàËÆ¶È:76.6% 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 45 . ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:76.6% Natural Product Research 2008 22 154-166 Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis S. H. Qi; S. Zhang; L. H. Yang; P. Y. Qian Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:76.6% China Journal of Chinese Materia Medica 2007 32 235-237 Studies on chemical constituents from the fruiting bodies of Ganoderma sinense Zhao,Xu et Zhang LIU Chao , WANG Hongqing, LI Baoming, CHEN Ruoyun Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:76.6% Journal of Natural Products 1987 Vol 50 915 Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Vincenzo Piccialli, Donato Sica Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene) C28H46O3 ÏàËÆ¶È:76.6% Phytochemistry 1991 30 4117-4120 Glycosides of ergosterol derivatives from Hericum erinacens Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 24-methyl-cholesta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Chinese Journal of Marine Drugs 2011 30(1) 31-36 Studies on Chemical Constituents of Subergorgia ret iculata LI Jun, LI Yong-ai, XU Jing, TANG Xu-li, LI Ping-lin, LI Guo-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . (3¦Â,5¦Á,6¦Á,7¦Â,22E)-ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:76.6% Chinese Journal of Marine Drugs 2008 27(4) 9-13 Studies on the chemical constituents from the endophytic fungus Penicillium sp.091402 of managrove plant Brugurera sexangula HAN Zhuang, MEI Wen-li, CUI Hai-bin, LIN Hai-peng, HONG Kui, DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:76.6% Indian Journal of Chemistry 2005 44B 1291-1294 Sterols and flavonol glycosides from Melothria purpusila Langoljam,Reena D; Kongbrailatpam,Brajeshwari D; Laitonjam,Warjeet S Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . ( 22 E)-3¦Â-Acetoxv-5 ¦Á-hydroxyergosta-7,22-dien-6-one ÏàËÆ¶È:76.6% Steroids 1996 61 540-543 New synthetic strategy for the synthesis of 24-epibrassinolide Carme Brosa, Rita Puig, Xavier Comas, Cristina Fern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Chinese Traditional and Herbal Drugs 2010 41 1065-1068 СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿ Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Chinese Traditional and Herbal Drugs 2008 39 1606-1609 Chemical constituents of Amtipathes dichotoma SU Guo-chen; ZHANG Si; QI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol C28H46O3 ÏàËÆ¶È:76.6% Chinese Traditional and Herbal Drugs 1994 25 342-343+390 Studies on the Chemical Constituents of Kuhonggu (Russula rosacea)(¢ò) Wang Huaibin; Xu Weishen; et al(Institute of Materia Medica; Chinese Academy of Medica Sciences; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . 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Cerevisterol ÏàËÆ¶È:76.6% Archives of Pharmacal Research 2006 29 479-483 Constituents from the fruiting bodies of Ganoderma applanatum and their aldose reductase inhibitory activity Sang Hyun Lee, Sang Hee Shim, Ju Sun Kim and Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . (22E,24R)-ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Archives of Pharmacal Research 2007 30 28-33 Cytotoxic constituents isolated from the fruit bodies of Hypsizigus marmoreus Ming-Lu Xu, Jae-Young Choi, Byeong-Seon Jeong, Gao Li and Kap-Rang Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:76.6% Chinese Pharmaceutical Journal 2006 41 1131-1133 Chemical Constituents of Monascus anka LI Li-li, CHEN Jie-peng, KONG Ling-yi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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