| ²é¿´: 248 | »Ø¸´: 1 | ||||
dysoxylumÒø³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
άÆÕÇóÖú
|
|
CÆ×Êý¾ÝÈçÏ£º 13C NMR (201 MHz, Pyr)£º15.07,19.75,20.60,21.84,22.86,23.21,23.55,26.01,30.06,32.02,39.05,43.50,43.73,46.73,49.03,52.33,56.18,68.56,77.86,110.85,121.10,126.10,139.36,142.26,144.08,154.64,167.31,168.96,173.09,175.02,179.23,203.66 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
dysoxylum: ½ð±Ò+12 2013-08-29 17:11:34
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
dysoxylum: ½ð±Ò+12 2013-08-29 17:11:34
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½419¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . andirobin C27H32O7 ÏàËÆ¶È:68.7% Phytochemical Analysis 2009 20 77-81 Isolation of Limonoids from seeds of Carapa guianensis Aublet (Meliaceae) by high-speed countercurrent chromatography Vagner Pereira da Silva, Rodrigo Rodrigues Oliveira and Maria Raquel Figueiredo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 11¦Â-hydroxygedunin C28H34O8 ÏàËÆ¶È:65.6% Journal of Natural Products 2006 69(9) 1310-1314 Hydroxylated Gedunin Derivatives from Cedrela sinensis Kumiko Mitsui, Hiroaki Saito, Ryota Yamamura, Haruhiko Fukaya, Yukio Hitotsuyanagi, and Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 14¦Â,15¦Â-epoxyazadirone ÏàËÆ¶È:62.5% Phytochemistry 1994 37 1417-1420 Limonoids and triterpenoid acids from the bark of Entandrophragma delevoyi Dulcie A. Mulholland, Roy Osborne, Sianne L. Roberts, David A.H. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . thaimoluccensin A C27H36O8 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry Letters 2011 21 4485-4489 Limonoids from seeds of Thai Xylocarpus moluccensis Warin Ravangpai, Damrong Sommit, Thapong Teerawatananond, Nuntawan Sinpranee, Tanapat Palaga, Somchai Pengpreecha, Nongnuj Muangsin, Khanitha Pudhom Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2'S-cipadesin ÏàËÆ¶È:59.3% Journal of Natural Products 2007 70 1344-1347 Tetranortriterpenoids from Cipadessa baccifera Li-She Gan, Xiao-Ning Wang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 29-hydroxystelliferin A C32H48O5 ÏàËÆ¶È:59.3% Journal of Natural Products 2001 64 389-392 New Cytotoxic Isomalabaricane Triterpenes from the Sponge Jaspis Species Karina M. Meragelman, Tawnya C. McKee, and Michael R. Boyd Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 4 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1996 44 847-849 Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . secomahoganin C29H36O9 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1990 38 1495-1500 Constituents of the Seeds of Swietenia mahagoni JACQ. III. : Structures of Mahonin and Secomahoganin Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . secomahoganin C29H36O9 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1989 37 1419-1421 MAHONIN AND SECOMAHOGANIN, NEW TETRANORTRITERPENOIDS FROM SWIETENIA MAHOGANI (L.) JACQ Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl 3¦Â-tigloyloxy-2-hydroxy-1-oxo-meliac-8(30)-enate C32H40O9 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6-desoxyswietenine C32H40O8 ÏàËÆ¶È:59.3% 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 12 . sandoricin C31H40O11 ÏàËÆ¶È:59.3% Journal of Natural Products 1991 Vol 54 241 Limonoid Antifeedants from Seed of Sandoricum koetjape Richard G. Powell, Kenneth L. Mikolajczak, Bruce W. Zilkowski, Ellen K. Mantus, David Cherry, Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Toonacilin ÏàËÆ¶È:59.3% Phytochemistry 1995 38 397-401 Limonoids from seeds of Toona ciliata and their chemosystematic significance João Oiano Neto, Sueli M.M. Agostinho, M.F¨¢tima Das G.F.Da Silva, Paulo C. Vieira, João B. Fernandes, Antônio L. Pinheiro, Evaldo F. Vilela Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cipadesin ÏàËÆ¶È:59.3% 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 15 . anthothecol ÏàËÆ¶È:59.3% Journal of the Chemical Society, Perkin Transactions 1 1975 1758-1764 The structures of three new meliacins isolated from Khaya anthotheca heartwood Thomas G. Halsall and Jeffrey A. Troke Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 6¦Á-acetoxygedunin ÏàËÆ¶È:59.3% Indian Journal of Chemistry 1989 28B 231-236 Chemistry of phyto-constituents of Chisocheton paniculatus Hiern(Meliaceae) A Chatterjee, L Nayak, B Das, A Patra, K P Dhara, K Mukherjee & J Banerji Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 4 C28H32O7 ÏàËÆ¶È:59.3% Phytochemistry Letters 2012 5 486-489 Fluorinated and rearranged gedunin derivatives Yukio Hitotsuyanagi, Kumiko Mitsui, Haruhiko Fukaya, Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 4 C36H48O12 ÏàËÆ¶È:58.3% Phytochemistry 1981 20 2263-2265 Ekebergin, a limonoid extractive from Ekebergia capensis David A.H. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 23-galloylterminolic acid C37H52O10 ÏàËÆ¶È:57.1% Journal of Natural Products 2002 65 1909-1914 Fatty Acid Synthase Inhibitors from Plants: Isolation, Structure Elucidation, and SAR Studies Xing-Cong Li,Alpana S. Joshi,Hala N. ElSohly, Shabana I. Khan, Melissa R. Jacob, Zhizheng Zhang,Ikhlas A. Khan, Daneel Ferreira, Larry A. Walker, Sheldon E. Broedel, Jr., Robert E. Raulli, and Ronald L. Cihlar Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . swietmanin J C27H34O7 ÏàËÆ¶È:56.2% Journal of Natural Products 2009 72 2084-2090 Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni Bing-Dong Lin, Tao Yuan, Chuan-Rui Zhang, Lei Dong, Bo Zhang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 11¦Â-acetoxygedunin C30H36O9 ÏàËÆ¶È:56.2% Journal of Natural Products 2006 69(9) 1310-1314 Hydroxylated Gedunin Derivatives from Cedrela sinensis Kumiko Mitsui, Hiroaki Saito, Ryota Yamamura, Haruhiko Fukaya, Yukio Hitotsuyanagi, and Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2'R-cipadesin ÏàËÆ¶È:56.2% Journal of Natural Products 2007 70 1344-1347 Tetranortriterpenoids from Cipadessa baccifera Li-She Gan, Xiao-Ning Wang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . hirtin C32H36O11 ÏàËÆ¶È:56.2% Journal of Natural Products 2001 64 1117-1120 Insect Antifeedant Activity of Three New Tetranortriterpenoids from Trichilia pallida Monique S. J. Simmonds,Philip C. Stevenson, Elaine A. Porter, and Nigel C. Veitch Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 14,15-deoxytoonacilin C31H38O8 ÏàËÆ¶È:56.2% Planta Medica 1992 58 712 A New Limonoid from the Seed of Turraea floribunda D. A. Mullholland, IL. Fraser, and J. J. Nair Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . cipadesin C32H48O8 ÏàËÆ¶È:56.2% Phytochemistry 2000 55 867-872 Components of Cipadessa baccifera Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, Da-Gang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-29 16:26:51














»Ø¸´´ËÂ¥