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hycomeľ³æ (ÕýʽдÊÖ)
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ÇóÖú C Æ× ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (151 MHz, CDCl3) ¦Ä 135.56,135.35,132.48,130.90,79.59,66.63,56.38,53.56,51.84,51.27,44.73,42.93,39.86,39.51,37.09,34.85,33.22,30.27,29.85,28.78,23.56,20.78,20.09,19.78,17.70,13.02. |
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hycome: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-04-17 01:49:56
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hycome: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-04-17 01:49:56
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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£º¹²²éµ½538¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5¦Á,8¦Á-epidioxiergosta-6,22-dien-3¦Â-ol ÏàËÆ¶È:89.2% Annals of Microbiology 2012 62 601-607 Structural characterization and metabolite profiling of the facultative marine fungus Paecilomyces variotii Francisco Javier Toledo Marante, Roberto Mioso, Jaime Bermejo Barrera, Juan Emilio Gonz¨¢lez Gonz¨¢lez, Juan Jos¨¦ Santana Rodr¨ªguez, Irma Herrera Bravo de Laguna Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â-hydroxy-5¦Á,8¦Á-epidioxyergosta-6,22-diene ÏàËÆ¶È:89.2% Chinese Traditional and Herbal Drugs 2014 45 1047-1051 Anthraquinone compounds from rhizome of Smilax scobinicaulis ZHANGMin, WANG Qi, XU Jing, CHEN Tao, SUN Wei, ZHANG Cun-li, FENG Shi-xiu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxy-5¦Á,8¦Á-epidioxyergosta-6,22-diene C28H44O3 ÏàËÆ¶È:88.8% Journal of Asian Natural Products Research 2001 3 299-311 CONSTITUENTS FROM LIMONIA CRENULATA XUE-ME1 NIU, SHENG-HONG LI, LI-YAN PENG,and HAN-DONG SUN,ZHONG-WEN LIN, GAO-XIONG RAO Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5¦Á,8¦Á-epidioxy-24(R)-methycholesta-6,22-dien-3¦Â-ol ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2006 31 304-306 Studies on chemical constutuents in stem of Dendrobium chrysotoxum GONG Yanqing, YANG Hong, LIU Yun, LIANG Aiqun, WANG Zhengtao, XU Luoshan, HU Zhibi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ergosterol peroxide ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2006 31 1078-1080 Chemical constituents from branch of Broussonetia papyrifera CHAO Jianfei, YIN Zhiqi, YE Wencai, ZHAO Shou xun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5¦Á,8¦Á-epidioxy-ergosta-6,22-diene-3¦Â-ol ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2005 30 351-353 Studies on constituents from the fermentation of Alternalia sp. ZHANG Hailong, TIAN Li, FU Hongwei, PEI Yuehu, HUA Huiming Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á,8¦Á-peroxyergosterol ÏàËÆ¶È:88.8% Natural Product Sciences 2004 10 306-309 Triterpenoids from Orostachys japonicus Lee, Sang-Hyun; Paek, Sun-Ha; Kim, Seung-Ki; Kim, Bak-Kwang; Shin, Kuk-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ |
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