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xp¡ªflyÌú¸Ëľ³æ (ÖøÃûдÊÖ)
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΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 16ºÅ 13C NMR (151 MHz, MeOD) ¦Ä 15.90, 16.31, 16.62, 25.61, 26.10, 26.96, 27.27, 30.52, 38.84, 39.20, 40.44, 40.54, 60.09, 61.72, 68.25, 70.47, 70.82, 71.05, 72.61, 76.31, 76.49, 76.69, 76.95, 77.11, 77.78, 78.34, 100.23, 103.12, 104.01, 135.64. |
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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xp¡ªfly: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-04 08:35:20
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xp¡ªfly: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-04 08:35:20
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²éѯ½á¹û£º¹²²éµ½3¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 27-hydroxyl-20(S)-protopanaxatriol C30H52O5 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 678-680 Microbial Transformation of 20(S)-Protopanaxatriol by Mucor spinosus Yin Tian, Hongzhu Guo, Jian Han, and Dean Guo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 3 C125H209N9O69S ÏàËÆ¶È:60% Carbohydrate Research 2006 341 1341-1352 Synthesis of a novel glycosphingolipid from the millipede, Parafontaria laminata armigera, and the assembly of its carbohydrate moiety into multivalent structures Noriyasu Hada, Yoshiko Sonoda, Tadahiro Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 26-Hydroxyl-24(E)-20(S)-protopanaxtriol C30H52O5 ÏàËÆ¶È:60% Journal of Natural Medicines 2012 66 576-582 Three new triterpenoids from Panax ginseng exhibit cytotoxicity against human A549 and Hep-3B cell lines Hai-Ying Ma, Hui-Yuan Gao, Jian Huang, Bo-hang Sun and Bo Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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