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zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-23 17:09:31
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²éѯ½á¹û£º¹²²éµ½17113¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . methyl 3¦Â-tigloyloxy-2-hydroxy-1-oxo-meliac-8(30)-enate C32H40O9 ÏàËÆ¶È:88.2% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl-2-hydroxy-3¦Â-tigloyloxy-1-oxomeliac-8(30)-enate ÏàËÆ¶È:88.2% Phytochemistry 1998 49 1981-1988 Limonoids from Swietenia humilis and Guarea grandiflora (Meliaceae)Taken in part from the PhD and MS theses of C. Villarreal and M. A. Jim¨¦nez, respectively. Adelina Jimenez, Claudina Villarreal, Ruben Alfredo Toscano, Mathew Cook, John T. Arnason, Robert Bye, Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . humilinolide C C34H42O10 ÏàËÆ¶È:88.2% Journal of Natural Products 1993 Vol 56 1567-1574 New Tetranortriterpenoids from Swietenia humilis Rosabel Segura-Correa, Rachel Mata, Ana Luisa Anaya, Blanca Hernandez-Bautista, Rene Villena, Manuel Soriano-Garcia, Robert Bye, Edelmira Linares Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ruageanin B C32H40O10 ÏàËÆ¶È:82.3% Journal of Natural Products 1996 59 544-547 Tetranortriterpenoids from Ruagea glabra Baldwin S. Mootoo and Russel Ramsewak Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl 3¦Â-tigloyloxy-2-hydroxy-8¦Á,30¦Á-epoxy-1-oxo-meliacate C32H40O10 ÏàËÆ¶È:82.3% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6-desoxyswietenine C32H40O8 ÏàËÆ¶È:82.3% Fitoterapia 1999 70 106-108 6-Desoxyswietenine, a tetranortriterpenoid from Swietenia mahogani T.R. Govindachari, B. Banumathy, Geetha Gopalakrishnan,G. Suresh Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . humilinolide E C34H42O11 ÏàËÆ¶È:82.3% Phytochemistry 1998 49 1981-1988 Limonoids from Swietenia humilis and Guarea grandiflora (Meliaceae)Taken in part from the PhD and MS theses of C. Villarreal and M. A. Jim¨¦nez, respectively. Adelina Jimenez, Claudina Villarreal, Ruben Alfredo Toscano, Mathew Cook, John T. Arnason, Robert Bye, Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . febrifugin ÏàËÆ¶È:82.3% Zeitschrift f¨¹r Naturforschung B 2005 60b 351-355 Limonoids from Cipadessa fruticosa Ana C. Leite, João B. Fernandes, M. F¨¢tima das G. F. da Silva, and Paulo C. Vieira Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 6-O-acetyl-2-hydroxyswietenin C34H42O11 ÏàËÆ¶È:82.3% Heterocycles 2004 63 389-399 Three New Mexicanolides from the Stem Bark of Swietenia mahogani Jacq. Mona M. G. Saad, Tetsuo Iwagawa, Hiroaki Okamura, Matsumi Doe, and Munehiro Nakatani* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-hydroxyswietemahonolide C32H40O10 ÏàËÆ¶È:82.3% Heterocycles 2004 63 389-399 Three New Mexicanolides from the Stem Bark of Swietenia mahogani Jacq. Mona M. G. Saad, Tetsuo Iwagawa, Hiroaki Okamura, Matsumi Doe, and Munehiro Nakatani* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-Hydroxy-3-O-tigloylswietenolide C32H40O10 ÏàËÆ¶È:82.3% Journal of Natural Medicines 2009 63 41-45 Antibacterial activity of two limonoids from Swietenia mahagoni against multiple-drug-resistant (MDR) bacterial strains A. K. M. Shahidur Rahman, A. K. Azad Chowdhury, Husne-Ara Ali, Sheikh Z. Raihan and Mohammad S. Ali, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . febrifugin ÏàËÆ¶È:82.3% Chinese Traditional and Herbal Drugs 2010 41 846-851 Chemical constituents in seeds of Indian mangrove Xylocarpus granatum YANG Xiao-bo; YANG Sheng-xin; LI Min-yi; PAN Jian-yu; ZHENG Yi-nan; WU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Thaixylomolin D C34H40O11 ÏàËÆ¶È:82.3% Phytochemistry Letters 2013 6 482-485 Thaixylomolins D¨CF, new limonoids from the Thai true mangrove, Xylocarpus moluccensis Jun Li, Min-Yi Li, Qiang Xiao, Patchara Pedpradab, Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Trichagmalin A C36H42O12 ÏàËÆ¶È:80.5% Journal of Natural Products 2011 74 152-157 Phragmalin-and Mexicanolide-Type Limonoids from the Leaves of Trichilia connaroides Qiang Zhang, Ying-Tong Di, Hong-Ping He, Xin Fang, Dong-Lin Chen, Xiao-Hui Yan, Feng Zhu, Ting-Quan Yang, Ling-Li Liu, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-angeloyl-3-detigloylruageanin B C32H40O10 ÏàËÆ¶È:79.4% Phytochemistry 2005 66 1100-1107 Mexicanolide limonoids from the Madagascan Meliaceae Quivisia papinae Philip H. Coombes , Dulcie A. Mulholland, Milijaona Randrianarivelojosia Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-O-tigloyl-6-O-acetylswietenolide C34H42O10 ÏàËÆ¶È:79.4% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . swietenine acetate ÏàËÆ¶È:79.4% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . swietemahonolide C32H40O9 ÏàËÆ¶È:79.4% Chemical & Pharmaceutical Bulletin 1990 38 894-901 Constitutents of the Seeds of Swietenia mahagoni JACQ.II. : Structures of Swietemahonin A, B, C, D, E, F, and G and Swietemahonolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . methyl 3¦Â-tigloyloxy-2,6-dihydroxy-1-oxo-meliac-8(30)-enate C32H40O10 ÏàËÆ¶È:79.4% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3-O-tigloyl-6-O-acetyl-swietenolide ÏàËÆ¶È:79.4% Journal of Natural Products 1994 Vol 57 1446 Structures of a New Limonoid and a New Triterpenoid Derivative from Pericarps of Trichilia connaroides Akira Inada, Mari Konishi, Hiroko Murata, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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