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| CD3OD:17.58,18.14,18.92,19.47,19.84,20.26,20.49,21.59,23.64,24.18,31.02,32.34,33.27,33.49,34.47,35.13,39.49,40.90,41.45,41.59,42.33,44.25,44.59,44.78,50.90,52.78,54.19,55.00,55.38,56.62,58.40,64.93,65.48,81.43,81.79,178.63,208.56. |
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ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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chenjjun1982: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-02 16:49:12
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chenjjun1982: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-02 16:49:12
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1 . 10¦Á,13¦Á,16¦Á-trihydroxy-9¦Á-methyl-15-oxo-20-nor-kauran-19-oic acid ¦Ã-lactone-17-yl-16'¦Á,17'-dihydroxy-15'-oxo-ent-kaur-19'-oate C40H56O10 ÏàËÆ¶È:65% Planta Medica 2004 70 540-550 Structure of Kaurane-Type Diterpenes from Parinari sprucei and their Potential Anticancer Activity Alessandra Braca,Annahil Armenise, Ivano Morelli,Jeannette Mendez,Qiuwen Mi,Hee-Byung Chai,Steven M. Swanson ,A. Douglas Kinghorn,Nunziatina De Tommasi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2¦Á,3¦Â-diacetoxy-12¦Á-bromoolean-28,13¦Â-olide C34H51BrO6 ÏàËÆ¶È:64.8% Phytochemistry 2013 94 229-237 Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei Antonio Martinez, Francisco Rivas, Alberto Perojil, Andres Parra, Andres Garcia-Granados, Antonia Fernandez-Vivas Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 35¦Â-ribosylhopane triacetate ÏàËÆ¶È:63.1% ChemBioChem 2014 15 2156−2161 Ribosylhopane, a Novel Bacterial Hopanoid, as Precursor of C35 Bacteriohopanepolyols in Streptomyces coelicolor A3(2) Wenjun Liu, Elias Sakr, Philippe Schaeffer, Helen M. Talbot, Janina Donisi, Thomas H rtner, Elmar Kannenberg, Eriko Takano, and Michel Rohmer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . ent-16¦Â-hydroxykauran-17-oic acid C30H34O2 ÏàËÆ¶È:62.5% Chinese Chemical Letters 2003 14 58-61 A New Diterpenoid Dimer from Annona glabra Nian Yun YANG, Li Juan TIAN, Zheng Mu MENG, Ying HAN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (4R*,5R*,7S*,10R*)-4-formamidoeudesman-11-ol C16H29NO2 ÏàËÆ¶È:62.1% Helvetica Chimica Acta 2008 Vol. 91 426 New Sesquiterpene Formamides from the Marine Sponge Axinyssa sp. Wen-Jian Lan, Hong-Ping Wan, Guo-Xi Li, Hou-Jin Li, Yun-Yun Chen, Cheng-Zhu Liao, Ji-Wen Caia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Pyrazoline derivative C32H52N2O2 ÏàËÆ¶È:62.1% Phytochemistry 1993 33 240-242 Tuberosic acid, a pentacyclic triterpene from Nephrolepsis tuberosa C.P. Dutta, Jayanta Banerjee, Gitali Datta, U.K. Som, Tadashi Eguchi, Chikako Murasaki, Katsumi Kakinuma, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 6 ÏàËÆ¶È:62.1% Tetrahedron Letters 1999 40 1681-1684 Novel bacterial triterpenoids of the hopane series from Nitrosomonas europaea and their significance for the formation of the C35 bacteriohopane skeleton Myriam Seemann, Philippe Bisseret, Jean-Philippe Tritz, Alan B. Hooper, Michel Rohmer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Sakurasosaponin ÏàËÆ¶È:62.1% Natural Product Communications 2010 5 365-368 Identification of Sakurasosaponin as a Cytotoxic Principlefrom Jacquinia flammea Alberto S¨¢nchez-Medina, Luis M. Peña-Rodr¨ªguez, Filogonio May-Pat, Gloria Karagianis,Peter G. Waterman, Anthony I. Mallet and Solomon Habtemariam* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (32S,33R,34R)-Bacteriohopanetetro-l ÏàËÆ¶È:62.1% Chinese Journal of Spectroscopy Laboratory 2009 26 718-720 Studies on Chemical Constituents from Ircinia Mutans Wilsion PANG Hui-Dai, LIAO Xiao-Jian, Xu Shi-Hai, XIONG Sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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