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C-NMR(pyr£¬600M): 12.4,17.7,18.7,19.7,20.0,21.3,22.2,23.3,28.4,32.5,33.2,33.7,37.9,39.7,40.8,41.8,42.9,43.6,55.1,55.9,67.4,74.1,76.0,120.4,131.9,141.4 [ Last edited by ׿Խ_ÏÈ·æ on 2015-5-11 at 15:07 ] |
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yylkmb: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄãµÄ°ïÖú 2015-05-11 17:40:40
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yylkmb: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄãµÄ°ïÖú 2015-05-11 17:40:40
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²éѯ½á¹û£º¹²²éµ½1324¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 24-Methylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:96.2% 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 2 . (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:96.2% 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 3 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:96.2% 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 4 . (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:96.2% Chinese Journal of Applied & Environmental Biology 2005 11 67-70 STEROLS FROM ASPERGILLUS OCHRACEUS 43 LI Guoyou; LI Bogang; LIU Guangye & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:96.2% Natural Product Research and Development 2012 24 1047-1050 Secondary Metabolites from Marine Fungus Fusarium sp. LIU Tao; LI Zhan-lin; WANG Yu; TIAN Li; PEI Yue-hu; HUA Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¾Æ½ÍĸçÞ´¼ ÏàËÆ¶È:96.2% 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 7 . (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:96.2% Journal of Jinan University (Natural Science) 2009 30 556-559 Studies on chemical constitutents of petroleum ether extract with anti-tumor activity from Nerviliae fordii LU Chuan-i, WANG Hui, ZHOU Guang-xiong, WANG Heng-shan, YE Wen-cai, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 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 9 . ergosta-7,22-diene-3,5,6-triol |
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