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ÑùÆ·£¨6e-82£©CÆ×Êý¾ÝÈçÏ£º13C NMR (151 MHz, Pyr)
15.71,20.61,21.04,22.57,22.73,22.82,23.99,33.46,38.06,39.65,41.19,44.20,49.57,52.96,53.16,55.47,73.00,79.57,79.93,111.28,113.66,121.49,129.81,137.16,142.83,144.13,161.26,165.25,170.40,170.47,171.39,213.29
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1 .     cineracipadesin D
C31H40O10     ÏàËÆ¶È:62.5%
Journal of Natural Products          2009          72          714-718
Tetranortriterpenoids from the Leaves of Cipadessa cinerascens
Xin Fang, Ying-Tong Di, Chun-Shun Li, Zhao-Liang Geng, Zhen Zhang, Yu Zhang,Yang Lu, Qi-Tai Zheng,Shi-Yin Yang,and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ¦¤8¨C30,14¨C153¦Â-acetoxy-1-oxo-methylmeliacate
     ÏàËÆ¶È:62.5%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     6-acetoxyseneganolide A
C29H34O9     ÏàËÆ¶È:62.5%
Fitoterapia          2004          75          566-572
Antifungal limonoids from the fruits of Khaya senegalensis
Samir A.M. Abdelgaleil, Tetsuo Iwagawa, Matsumi Doec, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     khayalenoid F
C31H36O11     ÏàËÆ¶È:62.5%
Journal of Natural Products          2010          73          669-674
Limonoids and Triterpenoids from Khaya senegalensis
Tao Yuan, Chuan-Rui Zhang, Sheng-Ping Yang and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     humilinolide D
C31H38O11     ÏàËÆ¶È:62.5%
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

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6 .     3¦Â-acetoxy-1-oxo-¡÷8(10),14(15) methyl meliacate
     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1974                   437-441
13 C nuclear magnetic resonance spectra of some limonoids. Part I. The structure of procerin, an extractive from Carapa procera
David A. H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Methyl 6-acetoxyangolensate
C29H36O9     ÏàËÆ¶È:62.5%
Natural Product Research and Development          2013          25          581-584
Limonoids from the Twigs and Leaves of Swietenia macrophylla
ZHANG Rong, CAO Ming-ming, HE Hong-ping, ZHANG Yu, DI Ying-tong, HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     granatumin A
C31H36O8     ÏàËÆ¶È:59.3%
Journal of Natural Products          2009          72          2110-2114
Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum
Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3,6-O,O-diacetylswietenolide
31H38O10     ÏàËÆ¶È:59.3%
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

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10 .     1' ,4' ,16,17-Tetrahydro-3¦Â-acetoxy-1' -acetyl-6' -methoxy-4' -methyl-(16¦Á,17¦Á)-androsta-5,16-dieno[17,16-b]quinoline
C32H43NO4     ÏàËÆ¶È:59.3%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Ang¨¦la Magyar, J¨¢nos Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     xylomexicanolide A
C31H38O8     ÏàËÆ¶È:59.3%
Chemical & Pharmaceutical Bulletin          2010          58          552-555
Mexicanolides from the Seeds of a Krishna Mangrove, Xylocarpus moluccensis
Jing Zhang, Sheng-Xin Yang, Xiao-Bo Yang, Min-Yi Li, Gang Feng, Jian-Yu Pan, Tirumani Satyanandamurty and Jun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     indiangranatumin A
     ÏàËÆ¶È:59.3%
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

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13 .     Methyl 6-acetoxyangolensate
C29H36O9     ÏàËÆ¶È:59.3%
Tetrahedron          2001          57          119-126
Khayanolides, rearranged phragmalin limonoid antifeedants from Khaya senegalensis
Samir A.M Abdelgaleil, Hiroaki Okamura, Tetsuo Iwagawa, Atsuko Sato, Ikuko Miyahara, Matsumi Doe, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     moluccensin U
C32H40O10     ÏàËÆ¶È:59.3%
Journal of Natural Products          2012          75          1277-1283
Moluccensins R¨CY, Limonoids from the Seeds of a Mangrove, Xylocarpus moluccensis
Jun Li, Min-Yi Li, Gang Feng, Jing Zhang, Maarit Karonen, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     xylogodavarin E
C29H34O9     ÏàËÆ¶È:59.3%
Chemistry-A European Journal          2012          18          14342-14351
Andhraxylocarpins A¨CE: Structurally Intriguing Limonoids from the True Mangroves Xylocarpus granatum and Xylocarpus moluccensis
Jun Li, Dr. Min-Yi Li, Dr. Torsten Bruhn, Dr. Daniel C. G. Götz, Prof. Dr. Qiang Xiao, Tirumani Satyanandamurty, Prof. Dr. Jun Wu and Prof. Dr. Gerhard Bringmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     granatumin B
C32H40O8     ÏàËÆ¶È:56.2%
Journal of Natural Products          2009          72          2110-2114
Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum
Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     domesticulide D
C29H36O11     ÏàËÆ¶È:56.2%
Phytochemistry          2006          67          2288-2293
Antimalarial tetranortriterpenoids from the seeds of Lansium domesticum Corr.
Nisakorn Saewan, John D. Sutherland, Kan Chantrapromma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 11a
C35H56O6     ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          1988          36          153-161
Saponin and Sapogenol. XLI. : Reinvestigation of the Structures of Soyasapogenols A, B, and E, Oleanene-Sapogenols from Soybean. Structures of Soyasaponins I, II, and III
ISAO KITAGAWA,HUI KANG WANG,TOSHIO TANIYAMA and MASAYUKI YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     humilinolide D
     ÏàËÆ¶È:56.2%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     humilinolide E
     ÏàËÆ¶È:56.2%
Natural Product Research          2008          22          763-800
13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family
T. Narender; T. Khaliq; Shweta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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