| ²é¿´: 513 | »Ø¸´: 1 | ||||
20071070088Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÊý¾Ý²éѯ
|
| CÆ×ÈçÏ£º13C NMR (126 MHz, CDCl3)£º16.50,17.16,17.26,21.23,21.27,21.49,27.96,28.40,32.58,35.96,37.66,38.79,41.03,44.83,45.34,53.53,53.60,65.54,74.33,75.70,78.26,109.86,141.16,143.29,169.28,209.26 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
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´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú¼ìË÷άÆÕ13CNMRÊý¾Ý,лл£¡
ÒѾÓÐ9È˻ظ´
άÆÕÊý¾ÝÇóÖú£¡
ÒѾÓÐ5È˻ظ´
άÆÕÇóÖú£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆÕÊý¾Ý£¡¼±£¡¼±£¡¼±£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúάÆÕÊý¾Ý¿âÎÄÏ×һƪ
ÒѾÓÐ1È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢ÆÕÊý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ6È˻ظ´
ÁÙ´²ÊÔÑéÊý¾Ý²éѯ
ÒѾÓÐ7È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
Çó²éάÆÕÊý¾Ý£¬ÍƲ⻯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú¹ØÓÚ»¯ºÏÎïÀí»¯ÐÔÖʲéѯµÄÍøÕ¾ºÍÊý¾Ý¿â
ÒѾÓÐ9È˻ظ´
ÇëÇó²éѯÎÒµÄÂÛÎĵÄSCI¼ìË÷ºÅ£¬ÎÒÃÇѧУûÓÐÊý¾Ý¿â¡£
ÒѾÓÐ6È˻ظ´
¡¾ÌÖÂÛ¡¿ÇóÖú£º£ºNOTEEXPRESS Ö±½ÓÁ¬ÏßάÆÕÊý¾Ý¿âÏÂÔØÈ«ÎÄ
ÒѾÓÐ3È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
20071070088: ½ð±Ò+10 2013-08-29 20:07:41
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
20071070088: ½ð±Ò+10 2013-08-29 20:07:41
|
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£º¹²²éµ½801¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . andirolide I C26H30O7 ÏàËÆ¶È:76.9% Tetrahedron 2012 68 3669-3677 Andirolides H¨CP from the flower of andiroba (Carapa guianensis, Meliaceae) Yuji Tanaka, Asami Sakamoto, Takanobu Inoue, Takeshi Yamada, Takashi Kikuchi, Tetsuya Kajimoto, Osamu Muraoka, Akira Sato, Yusuke Wataya, Hye-Sook Kim, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-oxokhivorin ÏàËÆ¶È:73.3% 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 ̼Æ×Ä£Äâͼ 3 . 7-oxo-khivorin ÏàËÆ¶È:73.3% 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 ̼Æ×Ä£Äâͼ 4 . Compound EX-1-5 ÏàËÆ¶È:67.8% Journal of Natural Medicines 2006 60 240-242 Isolation of cytochrome P450 3A (CYP3A) inhibitors from Hyuganatsu, Citrus tamurana Hort. Shinzo Hosoi, Eri Shimizu, Noriyuki Usami, Ikuo Yamamoto and Kazuhiko Arimori, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ÄÖÃ×ÁÖ ÏàËÆ¶È:67.8% Journal of Shenyang Pharmaceutical University 2000 17 253-255 Chemical Constituents of the Peels of Citrus Grandis Feng Baomin, Pei Yuehu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . nomilin ÏàËÆ¶È:67.8% Zeitschrift f¨¹r Naturforschung C 2007 62 179-188 Red Mexican Grapefruit: A Novel Source for Bioactive Limonoids and their Antioxidant Activity K. K. Mandadi, G. K. Jayaprakasha, N. G. Bhat, and B. S. Patil Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . nomilin C28H34O9 ÏàËÆ¶È:67.8% Acta Scientiarum Naturalium Universitatis Sunyatseni 1995 34(4) 117-121 Studies on the Chemical Constituents of the Shatinyu Seeds Lai Zuoqi, Fu Xiong Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Nomilin ÏàËÆ¶È:67.8% Journal of the Science of Food and Agriculture 2007 87 1699-1709 Purification of citrus limonoids and their differential inhibitory effects on human cytochrome P450 enzymes Shibu M Poulose, Guddadarangavvanahally K Jayaprakasha, Richard T Mayer, Basavaraj Girennavar and Bhimanagouda S Patil Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 7-deacetoxy-7-oxogedunin C26H30O6 ÏàËÆ¶È:65.3% 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 ̼Æ×Ä£Äâͼ 10 . 7-oxogedunin ÏàËÆ¶È:65.3% 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 ̼Æ×Ä£Äâͼ 11 . nomilin ÏàËÆ¶È:64.2% Food Chemistry 2011 127 394-403 Chemical composition and biological activity of Citrus jambhiri Lush Dalia Hamdan, Mahmoud Zaki El-Readi, Ahmad Tahrani, Florian Herrmann, Dorothea Kaufmann, Nawal Farrag, Assem El-Shazly, Michael Wink Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . momilin ÏàËÆ¶È:64.2% Indian Journal of Chemistry 1997 36B 374-376 Two new limonoids from the seed of Microula sikkimensin H. Shangzhen Zhen, Juncai Meng, Xuwei Shen & Dinyun Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . nomilin C28H34O9 ÏàËÆ¶È:64.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 1995 34(4) 117-121 Studies on the Chemical Constituents of the Shatinyu Seeds Lai Zuoqi, Fu Xiong Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ekeberin C1 C26H32O6 ÏàËÆ¶È:61.5% Journal of Natural Products 2008 71(2) 167-174 Antiplasmodial Triterpenoids from Ekebergia capensis Toshihiro Murata, Toshio Miyase, Francis Wamakima Muregi, Yasuko Naoshima-Ishibashi, Kaoru Umehara, Tsutomu Warashina, Shigeyuki Kanou, Gerald M. Mkoji, Mamoru Terada, and Akira Ishih Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 16¦Â,20(S)- diacetoxy-4,4,14-trimethylpregn-9(11)-en-3¦Â-ol ÏàËÆ¶È:61.5% Chemistry of Natural Compounds 1989 25 309-311 NEW TRITERPENE AGLYCON FROM THE HOLOTHURIAN Duasmodactyla kurilenis S. A. Avilov and A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-29 19:00:39














»Ø¸´´ËÂ¥