| ²é¿´: 420 | »Ø¸´: 1 | |||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾ÝÈçÏ£º11.1,14.2,16.0,18.3,21.2,21.2,21.9,26.1,28.8,32.6,40.2,40.4,42.7,45.8,47.3,57.4,63.9,64.7,68.5,72.0,73.9,74.6,77.5,93.5,113.2,124.1,140.6,142.1,169.0,170.3,174.1,212.6 |
» ²ÂÄãϲ»¶
µçÆø×¨Ë¶320Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸Î÷±±¹¤Òµ´óѧ289 085602
ÒѾÓÐ33È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ24È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ28È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ50È˻ظ´
Çóµ÷¼Á£¬262»úеר˶
ÒѾÓÐ8È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
347Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ47È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¼±£¡~~лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
¡¾Ô´´·ÖÏí¡¿»¹ÇóÖúô£ºÃâ·ÑµÄÆ×ͼÊý¾Ý¿â20¸ö£¨Ç××Ô²âÊÔ£¬È«²¿ÓÐЧ£©¡¾ÎÞÖØ¸´¡¿
ÒѾÓÐ190È˻ظ´

lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48813.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 19:20:29
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 19:20:29
|
²éѯ½á¹û£º¹²²éµ½982¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . trichilin B C35H46O13 ÏàËÆ¶È:73.5% Bulletin of the Chemical Society of Japan 1994 67 2468-2472 The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Trichilin B C35H46O13 ÏàËÆ¶È:71.4% Phytochemistry 1994 36 39-41 Limonoid antifeedants from chinese Melia azedarach Munehiro Nakatani, Ruo Chun Huang, Hiroaki Okamura, Hideo Naoki, Tetsuo Iwagawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 12-Deacetyltrichilin I ÏàËÆ¶È:69.6% Bioorganic & Medicinal Chemistry 1996 4 1355-1359 Cytotoxic trichilin-type limonoids from Melia azedarach Koichi Takeya, Zhi-Sheng Qiao, Chieko Hirobe, Hideji Itokawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . trichilin C C35H46O13 ÏàËÆ¶È:68.7% Journal of Natural Products 1998 61 179-184 Limonoids Showing Selective Toxicity to DNA Repair-Deficient Yeast and Other Constituents of Trichilia emetica A. A. Leslie Gunatilaka, Vanderlan da S. Bolzani, Ermias Dagne, Glenn A. Hofmann, Randall K. Johnson, Francis L. McCabe, Michael R. Mattern, and David G. I. Kingston Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . trichilins A C35H46O13 ÏàËÆ¶È:68.5% Journal of the American Chemical Society 1981 103 1228-1230 Isolation and structures of trichilins, antifeedants against the Southern army worm Munehiro Nakatani, John C. James, Koji Nakanishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 12¦Á-hydroxymeliatoxin B1 C35H46O13 ÏàËÆ¶È:68.5% Phytochemistry 2014 107 175-181 Limonoids from the fruits of Melia toosendan and their NF-¦ÊB modulating activities Guo-Yuan Zhu, Li-Ping Bai, Liang Liu, Zhi-Hong Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-Deacetyltrichilin H ÏàËÆ¶È:67.6% Bioorganic & Medicinal Chemistry 1996 4 1355-1359 Cytotoxic trichilin-type limonoids from Melia azedarach Koichi Takeya, Zhi-Sheng Qiao, Chieko Hirobe, Hideji Itokawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . mesendanin K C33H44O12 ÏàËÆ¶È:66.6% Planta Medica 2013 79 163-168 Cytotoxic Limonoids from Melia azedarach Yuan, Chun-Mao; Zhang, Yu; Tang, Gui-Hua; Li, Yan; He, Hong-Ping; Li, Shi-Fei; Hou, Li; Li, Xing-Yao; Di, Ying-Tong; Li, Shun-Lin; Hua, Hui-Ming; Hao, Xiao-Jiang: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Trichilin D C35H46O12 ÏàËÆ¶È:65.7% Phytochemistry 1994 36 39-41 Limonoid antifeedants from chinese Melia azedarach Munehiro Nakatani, Ruo Chun Huang, Hiroaki Okamura, Hideo Naoki, Tetsuo Iwagawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . trichilin D C35H46O12 ÏàËÆ¶È:65.7% Bulletin of the Chemical Society of Japan 1994 67 2468-2472 The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 12¦Á-hydroxymeliatoosenin I C35H46O13 ÏàËÆ¶È:65.7% Phytochemistry 2014 107 175-181 Limonoids from the fruits of Melia toosendan and their NF-¦ÊB modulating activities Guo-Yuan Zhu, Li-Ping Bai, Liang Liu, Zhi-Hong Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (1S,3aR,5S,6R,7S,7aR)-1-(1-Acetoxyethyl)octahydro-4-methylidene-7-[(2S)-2-methyloxiran-2-yl]-6-[(3-methylpentanoyl)oxy]-2-oxo-1H-inden-5-yl (2E)-4-Acetoxy-3-methylpent-2-enoate C31H44O10 ÏàËÆ¶È:65.6% Helvetica Chimica Acta 2006 Vol. 89 1387 New Oplopane-Type Sesquiterpenes from Ligularia narynensis Xue Gao, Chang-Jun Lin, Wei-Dong Xie, Tong Shen, and Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . flammolide C28H38O9 ÏàËÆ¶È:65.6% Planta Medica 1999 65 386-388 Flammolide: A C-14 Carboxylate Eudesmanolide from Seneclo flammeus Jinfeng Hu and Zhongjian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Meliarachin B C30H36O11 ÏàËÆ¶È:65.6% Helvetica Chimica Acta 2011 Vol. 94 1515-1526 Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . violide Q C32H44O12 ÏàËÆ¶È:65.6% Heterocycles 2005 65 607-617 Briarane Diterpenes from a Gorgonian Briareum Sp. Tetsuo Iwagawa,* Kazutaka Babazono, Munehiro Nakatani, Matsumi Doe, Yoshiki Morimoto, and Kaoru Takemura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 18 C30H40O7 ÏàËÆ¶È:65.6% Journal of the Chemical Society, Perkin Transactions 1 1979 2959-2964 Tetranortriterpenoids and related compounds. Part 22. New apotirucailol derivatives and tetranortriterpenoids from the wood and seeds of chisocheton paniculatus(meliaceae) Joseph D. Connolly, Cecilia Labb¨¦, David S. Rycroft and David A. H. Taylor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . azedarachin B ÏàËÆ¶È:65.6% Heterocycles 1999 50 595-609 Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity Munehiro Nakatani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . azedarachin B C32H42O11 ÏàËÆ¶È:65.6% Heterocycles 1997 45 1781-1786 Antifeeding Limonoids from Melia toosendan Jian-Bo Zhou, Yuji Minami, Fumio Yagi, Kenjiro Tadera, and Munehiro Nakatani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 12-O-deacetyltrichilin H C34H44O13 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 2005 53(10) 1362-1365 Cytotoxic Limonoids from Brazilian Melia azedarach Honglei ZHOU,Atsuko HAMAZAKI, Jose Domingos FONTANA, Hironobu TAKAHASHI,Carolina Bueno WANDSCHEER,and Yoshiyasu FUKUYAMA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-24 17:41:30













»Ø¸´´ËÂ¥