| ²é¿´: 395 | »Ø¸´: 1 | ||
ÄÍÄ͵Äñ×ÓÌú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×Êý¾ÝÈçÏ£º 12.3,18.2,20.1,20.5,21.6,22.2,24.0,28.3,29.2,31.6,34.4,36.5,40.8,41.4,41.8,44.4,44.8,51.9,57.4,68.2,73.7,76.1,78.9,121.1,133.3,137.0,143.7,209.8 ë®´ú¼×´¼ |
» ²ÂÄãϲ»¶
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ15È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ24È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì322
ÒѾÓÐ16È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
293µ÷¼Á
ÒѾÓÐ18È˻ظ´

Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄÍÄ͵Äñ×Ó: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл£¡ 2015-05-11 12:36:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÄÍÄ͵Äñ×Ó: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл£¡ 2015-05-11 12:36:20
|
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%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½468¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol C28H46O4 ÏàËÆ¶È:96.4% Chinese Journal of Medicinal Chemistry 2008 18 279-283 Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (22E,22R)-ergost-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol ÏàËÆ¶È:96.4% Chinese Journal of Marine Drugs 2013 32 8-12 Secondary metabolites from the fungus Engyodontium album associated with the South China Sea starfish Anthenea pentagonula E Heng-chao, ZHOU Wei, LIU Bao-shu, TANG Hua, SUN Peng, LI Ling, ZHANG Wen* Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol C34H54O8 ÏàËÆ¶È:96.4% European Journal of Plant Pathology 2012 134 239-247 Toxins from a symbiotic fungus, Leptographium qinlingensis associated with Dendroctonus armandi and their in vitro toxicities to Pinus armandi seedlings Xiao-Jun Li, Jin-Ming Gao, Hui Chen, An-Ling Zhang, Ming Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol C32H52O4 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 5 . topsentisterol C3 C29H48O4 ÏàËÆ¶È:86.2% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol ÏàËÆ¶È:85.7% Acta Botanica Sinica 2003 45 753-756 Steroids from the Fungus Pleurotus ostreatus ZHAN Zha-Jun, WANG Ying, YANG Sheng-Ping, YUE Jian-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 12 ÏàËÆ¶È:85.7% Steroids 1995 60 666-673 New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Rosa Carnuccio, Teresa Iuvone Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-tetraol C28H48O4 ÏàËÆ¶È:85.7% 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 9 . trihydroxyergosta-7,22-dien-3¦Â,5¦Á,6¦Â,9¦Á-tetraol |
2Â¥2015-05-11 11:18:29














»Ø¸´´ËÂ¥