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²éѯ½á¹û£º¹²²éµ½1636¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ergosta-5,7,---triene-3¦Â-ol ÏàËÆ¶È:88.4% Chinese Journal of Marine Drugs 2006 25(1) 6-10 Studies on the chemical constituents of the fermentation liquid from marine actinomyces Micromonos por a sp. and bacteria Ocea nos pi rillum sp. SHI Ying, TIAN Li, WANG Jing, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ergosta-5,7,22-t riene-3¦Â-ol ÏàËÆ¶È:88.4% Chinese Journal of Marine Drugs 2004 23(1) 14-16 Study on the chemical constituents of the fermentation liquid from marine fungus Aspergillus versicolor ZHANG Hai-long, MA Li, TIAN Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ergosterol derived ÏàËÆ¶È:88.4% Tetrahedron Letters 2000 41 2791-2795 Stereochemistry of hydrogen introduction at C-25 in ergosterol synthesized by the mevalonate-independent pathway Wen-xu Zhou, W. David Nes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Ergosterol ÏàËÆ¶È:88.4% 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 -------------------------------------------------------------------------------- 5 . ergosterol ÏàËÆ¶È:88% 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 -------------------------------------------------------------------------------- 6 . Ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:85.1% Helvetica Chimica Acta 2004 Vol. 87 1912 Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis Fei Wang, Jian-Wen Tan, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Âó½ÇçÞ´¼ C28H44O ÏàËÆ¶È:84.6% Chinese Traditional and Herbal Drugs 2004 35 493-495 È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿ Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 9 . ergosterol C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 10 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 11 . (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 12 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 13 . (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 14 . ¦Â-ergosterol ÏàËÆ¶È:82.1% Chinese Traditional and Herbal Drugs 2000 31 328-330 ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿ Íò»Ô Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 16 . ergosta-5, 7, 22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 17 . ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 18 . 22 E-ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 19 . (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼ C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 20 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 21 . Âó½ÇçÞ´¼ ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 22 . 24(R)-methylcholesta-5,7,22-tiene-3-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 23 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 24 . ergosterol C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 25 . (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:82.1% Natural Product Research and Development 2010 22 972-975 Chemical Constitutes of Termitomyces schimperi Collected from Africa YANG Xiao-long;ZHU Ying-cheng; FANG Sheng-tao; JIANG Meng-yuan; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . ergosta-5,7,22-trien-3-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 27 . (22E,24R)-ergosta-5,7,22-trine-3¦Â-ol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 28 . ergosta-5,7,22-trien-3¦Â-o-l C28H44O ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 29 . ¦Â-ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 30 . ergosterol ÏàËÆ¶È:82.1% 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 -------------------------------------------------------------------------------- 31 . ergosterol ÏàËÆ¶È:82.1% Chinese Traditional and Herbal Drugs 2011 42 251-254 Chemical constituents of Omphalia lapidescens XU Ming-feng, SHEN Lian-qing, WANG Kui-wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:82.1% Chinese Journal of Natural Medicines 2011 9 101-104 A New Biphenyl from the Fermentation Broth of Plant Endophytic Fungus Pestalotiopsis zonata isolated from Cyrtotachys lakka YANG Xiao-Long, *, ZHANG Su, SONG Shao-Jun, ZHANG Yan, LUO Du-Qiang,, ZHANG Meng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . Ergosta-5,7,22-trien-3¦Â-ol ergosterol C28H44O ÏàËÆ¶È:82.1% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . ergosterol ÏàËÆ¶È:82.1% Chinese Journal of Natural Medicines 2012 10 72-76 Bioactive metabolites from Guignardia sp., an endophytic fungus residing in Undaria pinnatifida Feng-Wu WANG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . Ergosterol C28H44O ÏàËÆ¶È:78.5% Chemistry of Natural Compounds 2009 45 759-761 STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . ergosterol ÏàËÆ¶È:78.5% 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 -------------------------------------------------------------------------------- 37 . ergosterol ÏàËÆ¶È:78.5% 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 -------------------------------------------------------------------------------- 38 . ergosterol ÏàËÆ¶È:78.5% Natural Product Research and Development 2010 22 422-424 Chemical Constituents from Fruiting Bodies of Phylloporia ribis(Lonicera japonica Thunb.) LI Cong; ZHANG Yong-qing; LI Jia; QIU Li-li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . ergoaterol ÏàËÆ¶È:78.5% 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 -------------------------------------------------------------------------------- 40 . Ergosterol C28H440 ÏàËÆ¶È:75% Chemistry of Natural Compounds 2000 36 170-172 LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.IV. SLIGHTLY POLAR COMPONENTS OF Stachybotrys alternans L. S. Kamalov, M. A. Agzamova,S. F. Aripova, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . ergosterol ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 1997 22 485-486 Studies on Chemical Constituents of Bulgaria inquinans (Fries) Cui Dongbin , Wang Shuqin and Ding Xiaokun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 24¦Â-methylcholesta-5,7,22,25-tetraen-3¦Â-ol ÏàËÆ¶È:75% 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 -------------------------------------------------------------------------------- 43 . ergosterol(3¦Â-hydroxyergosta-5,7,22-triene) C28H44O ÏàËÆ¶È:75% 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 -------------------------------------------------------------------------------- 44 . Âó½ÇçÞ-5,7,2-ÈýÏ©-3¦Â-´¼ ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2007 38 337-339 Chemical constituents of fruiting bodies from basidiomycete Suillus granulatus and their anti-HIV-1 activity DONG Ze-jun; WANG Fei; WANG Rui-rui; YANG Liu-meng; ZHENG Yong-tang; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . ergost-5,7,22-trien-3-ol ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2006 37 1297-1300 Chemical constituents of basidiomycete Coltricium nitidum DU Jian-chang; WANG Xing-na; TAN Ren-xiang; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . erogosterol C28H46O ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2003 38 499-5001 Studies on chemical constituents of Cordyceps sinensis(Berk) Sacc LI Jie-xiu, LI Jin, XU Li-zhen, YANG Shi-lin, ZOU Zhong-mei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . ergosta-5,7,22-trine-3-o-l ÏàËÆ¶È:75% Natural Product Research and Development 2007 19 809-810 Study on the Chemical Constituents of Lasiosphaera fenzlii Reich. WANG Xue-qin; SUN Long-ru* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . (22E,24R)-ergosta-5,7,22-triene-3¦Â-ol C28H44O ÏàËÆ¶È:75% 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 -------------------------------------------------------------------------------- 49 . compound 4 ÏàËÆ¶È:73.9% 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 -------------------------------------------------------------------------------- 50 . ergosta-5,7-dien-3¦Â-ol 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 -------------------------------------------------------------------------------- 51 . ×ØÍ©ËᵨçÞÏ©õ¥ ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 1998 29 298-300 ´óÂí²ªµÄ»¯Ñ§³É·ÖÑо¿ ½ðÏòȺ,ÍõÁ¥Êé,³Ì¶«ÑÒ,ÒÁѧÁú,ÂÀ¾°É½ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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