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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-23 16:53:26
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