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1 . cerevisterol C28H46O3 ÏàËÆ¶È:92.8% 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 2 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:92.8% Chemistry of Natural Compounds 2009 45 124-125 COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus Weiwei Zhou, Shunxing Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol) ÏàËÆ¶È:92.8% 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 4 . ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% 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 5 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:92.8% 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 6 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:92.8% 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 7 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:92.8% 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 8 . cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene) C28H46O3 ÏàËÆ¶È:92.8% 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 9 . ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:92.8% 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 10 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% 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 11 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:92.8% 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 12 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% 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 13 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol C28H46O3 ÏàËÆ¶È:92.8% 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 14 . cerevisterol ÏàËÆ¶È:92.8% Archives of Pharmacal Research 2005 28 889-891 Antibacterial constituents from fruit bodies of Ascomyce Bulgaria inquinans Peng Zhang, Xian Li, Ning Li, Jing Xu and Zhan-Lin Li, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (22E,24R)-ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% 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 16 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:92.8% 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 17 . ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol ÏàËÆ¶È:92.8% Chinese Pharmaceutical Journal 2010 45 413-415 A New Sterol from the Fruiting Bodies of Ganoderma sinense Zhao, Xu et Zhang LIU Chao, CHEN Ruo-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 22 E-ergosta-7,22-dien-3¦Â,5¦Â,6¦Â-triol ÏàËÆ¶È:92.8% 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 . (22E,24R)-ergos-ta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% Journal of Shenyang Pharmaceutical University 2009 26 796-799 Isolation and identification of steroids from the leaves of theMagnolia sieboldii K. Koch WANG Ru-ping, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:92.8% Journal of China Pharmaceutical University 2007 38 315-319 Chemical constituents of the aerial parts of Euphorbia sororia ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai; Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:92.8% Natural Product Research and Development 2007 19 436-438 Chemical Constituents of Basidiomycetes Russula subnigricans GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% 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 23 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol C28H44O2 ÏàËÆ¶È:92.8% Mycosystema 2009 28 407-409 Chemical components from the fruiting bodies of Ganoderma duropora ZHAO Fen LI Ye LIU Chao LI Bao-Ming CHEN Ruo-Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:92.8% Chinese Traditional and Herbal Drugs 2012 43 2365-2368 Study on chemical constituents in Cryptotaenia japonica LI Sheng-hua; NIU You-ya Key Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 8,9-epoxyergosta-5,22-dien-3¦Â,15-diol C28H44O3 ÏàËÆ¶È:89.6% 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 26 . (24R)-ergosta-7,22-diene-3,5,6-triol ÏàËÆ¶È:89.2% Chinese Journal of Natural Medicines 2008 6 348-353 Chemical Constituents of Marine Sponge Biemna fortis Topsent HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% 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 28 . 24-Methylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% 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 29 . (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.2% Natural Product Research and Development 2004 16 277-280 METABOLITES OF RHIZOPUS ARRHIZUS 3078 LI Guo-you; LI Bo-gang; LIU Guang-ye; ZHANG Guo-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.2% Biological and Pharmaceutical Bulletin 2002 25 1040-1044 Stimulative Effects of (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol from Fruiting Bodies of Tricholoma auratum, on a Mouse Osteoblastic Cell Line, MC3T3-E1 Keishi Hata, Fuyuki Sugawara, Naganori Ohisa, Saori Takahashi, Kazuyuki Hori Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% Chemistry of Natural Compounds 2012 48 913-913 Chemical constituents of basidiomycetes Cortinarius longipes Xiang-Dong Qin, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C10H13N5O4 ÏàËÆ¶È:89.2% Chinese Journal of Marine Drugs 2012 31 7-10 Secondary metabolites of marine fungus zp6 and their antifungal bioactivities GAO Chang-song; ZHONG Hui-min; CAO Jun-wei; CHEN Hao Structure 13C NMR ̼Æ×Ä£Äâͼ |
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