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²éѯ½á¹û£º¹²²éµ½1445¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 7 874-880 Studies on constituents of cultures of fungus Phellinu signiarius WU Xiu li,LIN Sheng, ZHU Chenggen, ZHAO Feng, YU Yang, YUE Zhenggang, LIU Bo,YANG Yong chun, DAI Jungui, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3¦Â,5¦Á,6¦Á,7¦Â,22E)-ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:85.7% 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 3 . cerevisterol C28H44O3 ÏàËÆ¶È:85.7% Chinese Traditional and Herbal Drugs 2009 40 1211-1214 Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿ ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (3¦Â,5¦Á,6¦Á,22E)-Âó½ÇçÞ-7,22-¶þÏ©-3,5,6-Èý´¼ C28H46O3 ÏàËÆ¶È:85.7% Chinese Journal of Medicinal Chemistry 2009 19 200-205 Chemical constituents from the endophytic fungus Acremonium sp. J1 of Antiaris toxicaria QUE Dong-mei, DAI Hao-fu, ZENG Yan-bo, WU Jiao, MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ergosta-7,11-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:85.7% Natural Product Research and Development 2010 22 235-237 Studies on the Chemical Constituents of Rhodobryum giganteum (schwaegr.) Par. JIAO Wei; LU Gai-li; SHAO Hua-wu; LU Run-hua; Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7,22-¶þÏ©-3,5,6-ÈýôÇ»ù-Âó½ÇçÞ´¼ ÏàËÆ¶È:85.7% Acta Scientiarum Naturalium Universitatis Sunyatseni 2001 40(4) 70-72 Metabolites of Marine Fungus Hypoxylon oceanicum from the South China Sea LI Hou-jin, UN Yong-cheng, WANG Li, ZHOU Shi-ning, L. L. P. RJJMOED Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cerevisterol C28H46O3 ÏàËÆ¶È:85.1% Chemistry of Natural Compounds 2011 47 858-861 Secondary metabolites of endophytic fungus Xylaria sp. YC-10 of Azadirachta indica Shao-Hua Wu, You-Wei Chen and Cui-Ping Miao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Globosterol C29H47O3 ÏàËÆ¶È:82.7% 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 . 24-methyl-cholesta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:82.1% 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 10 . (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:82.1% Chinese Traditional and Herbal Drugs 2005 36 1126-1130 Chemical constituents of basidiomycete Hydnum repandum WANG Xing-na; DU Jian-chang; TAN Ren-xiang; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:78.5% 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 12 . (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:75% 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 13 . dehydro ergosterol peroxide ÏàËÆ¶È:75% Archives of Pharmacal Research 1994 17 1-4 Some sesquiterpenoids and 5¦Á,8¦Á-epidioxysterols from Solanum lyratum Su Mi Yu, Hyoung Ja Kim, Eun-Rhan Woo and Hokoon Park Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ergosta-5, 7, 22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:75% Acta Bot. Boreal. -Occident. Sin. 2010 30 601-603 Chemical Constituents in the Fruiting Bodies of Sarcodon scabrosus MA Bing-ji, SHEN Jin-wen, YU Hai-you, ZHOU Hang, ZHAO Xu, RUAN Yuan, WU Ting-ting Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ergoaterol ÏàËÆ¶È:75% Natural Product Research and Development 2010 22 1018-1020 Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò) CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ergosterol ÏàËÆ¶È:72% China Journal of Chinese Materia Medica 2002 27 674-676 Studies on the Chemical Constituents of Shiraia bambusicola SHEN Yuxiu, RONG Xianguo, GAO Zonghua Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol C28H44O2 ÏàËÆ¶È:71.4% 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 . ergosterol ÏàËÆ¶È:71.4% Phytochemistry 1997 45 1669-1671 Ergosta-4, 6, 8, 22-tetraen-3-one from the edible fungus, Pleurotus ostreatus (oyster fungus) Vladimir Chobot, Lubom¨ªr Opletal, Ludk J¨¢hod¨¢, Asmita V. Patel, Christopher G. Dacke, Gerald Blunden Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ergosterol-7,22-dien-3¦Â-ol ÏàËÆ¶È:71.4% 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 20 . ergosterol C28H44O ÏàËÆ¶È:71.4% 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 21 . ergosterol ÏàËÆ¶È:71.4% Phytochemistry 1996 41 1301-1308 Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol ÏàËÆ¶È:71.4% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 541-544 BIOACTIVE METABOLITES FROM Penicillium sp. P-1,A FUNGAL ENDOPHYTE IN Huperzia serrata You-Min Ying, Zha-Jun Zhan, Zhi-Shan Ding,and Wei-Guang Shan Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ergosterol ÏàËÆ¶È:71.4% Phytochemistry 1990 29 2513-2520 Effect on ergosterol biosynthesis of a fungicide,SSF-109,in Botrytis cinerea Noboru Shirane,Akira Murabayashi,Michio Masuko,Atsuko Uomori,Yohko Yoshimura,Shujiro Seo,Kiyohisa Uchida,Ken'ichi Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ergosterol ÏàËÆ¶È:71.4% 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 25 . ¦Â-ergosterol ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2000 31 328-330 ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿ Íò»Ô Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . Ergosterol ÏàËÆ¶È:71.4% Archives of Pharmacal Research 2009 32 1573-1579 Steroids and triterpenes from the fruit bodies of Ganoderma lucidum and their anti-complement activity Hyo Won Seo, Tran Manh Hung, MinKyun Na, Hyun Ju Jung and Jin Cheol Kim, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:71.4% Chinese Pharmaceutical Journal 2009 44 418-421 Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 22 E-ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:71.4% Chinese Journal of Medicinal Chemistry 2006 16 98-101 The constituents of marine fungus 97F49 ZHANG Qing-hua, WANG Nai-li, GAO Hao, LIU Hong-wei, SONG Shan-shan, MICHIO Namikoshi, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼ C28H44O ÏàËÆ¶È:71.4% Chinese Journal of Medicinal Chemistry 2009 19 200-205 Chemical constituents from the endophytic fungus Acremonium sp. J1 of Antiaris toxicaria QUE Dong-mei, DAI Hao-fu, ZENG Yan-bo, WU Jiao, MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ergosterol ÏàËÆ¶È:71.4% Chemical Communications 1986 1139-1140 Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Âó½ÇçÞ´¼ ÏàËÆ¶È:71.4% Journal of Shenyang Pharmaceutical University 2007 24 245-248 Fermentation products of endophyte HCCB00167 XIE Cui-hua, RUAN Li-jun, XIA Huan-zhang, CHEN Dai-jie, GE Mei Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 24(R)-methylcholesta-5,7,22-tiene-3-ol ÏàËÆ¶È:71.4% Bulletin of the Korean Chemical Society 2008 29 615-619 Human Acyl-CoA: Cholesterol Acyltransferase (hACAT) Inhibitory Activities of Triterpenoids from Roots of Glycine max (L.) Merr. Jin Hwan Lee, Young Bae Ryu, Byong Won Lee, Jin Hyo Kim, Woo Song Lee, Yong-Dae Park, Tae-Sook Jeong, Ki Hun Park* Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ergosterol ÏàËÆ¶È:71.4% Bioscience, Biotechnology, and Biochemistry 1994 58 1542-1544 Volemolide, a Novel Norsterol from the Fungus Lactarius volemus Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ergosterol C28H44O ÏàËÆ¶È:71.4% Natural Product Research and Development 2010 22 998-1000 Chemical Constituents and Identification of the Caules of Clematis armandii Franch. and Clematis montana Buch.-Ham. LIU Jing-jing;CHEN Xing; WEI Zhi-qi; LI Bin Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ergosteryl palmitate ÏàËÆ¶È:71.4% Natural Product Research and Development 2010 22 1018-1020 Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò) CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . ergosta-5,7,22-trien-3-ol ÏàËÆ¶È:71.4% Natural Product Research and Development 2007 19 420-422 Isolation and Structures of Two Steroids from Mangrove Endophyte Penicillium sp. LI Xiang;SUN Guang-zhi; ZHENG Yi-nan; LIN Wen-han; Isabel Sattler Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (22E,24R)-ergosta-5,7,22-triene-3¦Â-ol C28H44O ÏàËÆ¶È:71.4% Natural Product Research and Development 2007 19 620-622 Chemical Constituents of Piper pedicellatum C. DC LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . ergosta-5,7,22-trien-3¦Â-o-l C28H44O ÏàËÆ¶È:71.4% Natural Product Research and Development 2004 16 204-206 THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS WANG Fei; LIU Ji-kai * Structure 13C NMR ̼Æ×Ä£Äâͼ |
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