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ÈܼÁ£ºDMSO C-NMR:10.07,14.49,16.67,22.68,23.32,23.38,23.44,23.56,26.59,33.36,34.46,34.74,36.57,38.24,41.64,42.75,43.10,43.22,43.58,68.20,68.48,123.70,123.98,124.61,124.91,126.15,126.36,134.36,134.72,135.43,145.25,145.43,157.52,157.84,179.68,179.91,185.48,185.87,186.42,186.47,198.86,199.01 |
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°×ÃæÍõ¹«×Ó: ½ð±Ò+5, ·Ç³£¸Ðл 2015-03-11 21:56:59
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°×ÃæÍõ¹«×Ó: ½ð±Ò+5, ·Ç³£¸Ðл 2015-03-11 21:56:59
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1 . Netzahualcoyonol ÏàËÆ¶È:51.4% Planta Medica 2001 67 65-69 Isolation and Frontier Molecular Orbital Investigation of Bioactive Quinone-Methide Triterpenoids from the Bark of Salacia petenensis William N. Setzer, Michael T. Holland, Carey A. Bozeman, Glenn F. Rozmus, Mary C. Setzer,Debra M. Moriarity, Sabine Reeb, Bernhard Vogler, Robert B. Bates, William A. Haber Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Á,3¦Á,24,28-tetrahydroxyolean-12-ene C30H50O4 ÏàËÆ¶È:51.4% Natural Product Research 2002 16 371-376 Highly Oxygenated Triterpenes from the Roots of Atropa Acuminata Arshad Mehmood; Abdul Malik; Itrat Anis; Pir Mohammad Khan; Muhammad Riaz; Talat Makhmoor; M. Iqbal Choudhary Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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