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wangwang1989
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ÖÐÔÂéȸ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-06-17 19:43:55
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½575¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cerevisterol C28H46O3 ÏàËÆ¶È:89.2% 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:89.2% 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 . ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% 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 4 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.2% 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 5 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:89.2% 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 6 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:89.2% 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 7 . cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene) C28H46O3 ÏàËÆ¶È:89.2% 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 8 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% 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 9 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.2% 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 10 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.2% 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 11 . cerevisterol ÏàËÆ¶È:89.2% 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 12 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:89.2% 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 |

2Â¥2013-06-17 19:24:38
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3Â¥2013-06-17 20:18:32
wangwang1989
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 525 (²©Ê¿)
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½579¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cerevisterol C28H46O3 ÏàËÆ¶È:89.6% 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 2 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:89.6% Chemistry of Natural Compounds 2009 45 124-125 COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus Weiwei Zhou, Shunxing Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.6% 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 4 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.6% 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 5 . 6,9-epidioxyergosta-7,22-dien-3¦Â-ol ÏàËÆ¶È:89.6% 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 6 . (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:89.6% 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 7 . cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene) C28H46O3 ÏàËÆ¶È:89.6% 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 8 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.6% 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 9 . stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:89.6% 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 10 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol C28H46O3 ÏàËÆ¶È:89.6% 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 11 . cerevisterol ÏàËÆ¶È:89.6% 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 12 . ergosta-7,22-diene-3,5,6-triol C28H46O3 ÏàËÆ¶È:89.6% 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 |

4Â¥2013-06-17 20:38:22
ÖÐÔÂéȸ
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5Â¥2013-06-17 20:46:09














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