| ²é¿´: 188 | »Ø¸´: 1 | ||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾ÝÈçÏ£º11.5,16.4,18.6,20.3,20.9,21.0,23.1,26.6,28.1,28.2,40.7,41.2,41.8,42.7,43.3,43.4,45.0,50.6,51.4,62.4,63.9,68.9,69.3,72.0,73.4,93.1,110.4,121.8,140.4,143.5,169.2,170.1,175.4,210.2,219.7 |
» ²ÂÄãϲ»¶
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
283·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
0703»¯Ñ§
ÒѾÓÐ23È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÃÌËáï®XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúάÆ×Êý¾Ý¿â
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- 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°¸ 2013-12-12 09:59:49
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 09:59:49
|
²éѯ½á¹û£º¹²²éµ½371¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Meliatoxin B1 ÏàËÆ¶È:97.1% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Trichilin D C35H46O12 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . trichilin D C35H46O12 ÏàËÆ¶È:71.4% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . neoazedarachin A ÏàËÆ¶È:65.7% Heterocycles 1999 50 595-609 Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . trichilins A C35H46O13 ÏàËÆ¶È:65.7% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Meliatoosenin J C37H48O14 ÏàËÆ¶È:64.8% Phytochemistry 2012 73 106-113 Limonoids from the fruits of Melia toosendan Yi Zhang, Chun-Ping Tang, Chang-Qiang Ke, Xi-Qiang Li, Hua Xie, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Trichilin H C36H46O14 ÏàËÆ¶È:63.8% Phytochemistry 1996 41 117-120 Limonoid antifeedants from Melia toosendan Jian-Bo Zhou, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Trichilin H C36H46O14 ÏàËÆ¶È:63.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . trichilin H C36H46O14 ÏàËÆ¶È:63.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . trichilin H ÏàËÆ¶È:63.8% Heterocycles 1999 50 595-609 Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Trichilin B C35H46O13 ÏàËÆ¶È:62.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Meliatoxin A2 C34H44O12 ÏàËÆ¶È:62.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-Deacetyltrichilin H ÏàËÆ¶È:62.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . trichilin B C35H46O13 ÏàËÆ¶È:62.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . meliatoxin A2 C34H44O12 ÏàËÆ¶È:62.8% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2,23-Di-O-acetylphyt O- laccagenin A ÏàËÆ¶È:62.1% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 1-Acetyl-3-deacetyltrichilin H C36H46O14 ÏàËÆ¶È:61.1% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 1-Acetyl-2-deacetyitrichilin H ÏàËÆ¶È:61.1% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . sanjecumin A C36H48O13 ÏàËÆ¶È:61.1% Journal of Natural Medicines 2012 66 Sanjecumins A and B: new limonoids from Sandoricum koetjape Yuta Nagakura • Alfarius Eko Nugroho • Yusuke Hirasawa •Takahiro Hosoya • Abdul Rahman • Idha Kusumawati •Noor Cholies Zaini • Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Sanjecumin A C36H48O13 ÏàËÆ¶È:61.1% Journal of Natural Medicines 2013 67 381-385 Sanjecumins A and B: new limonoids from Sandoricum koetjape Yuta Nagakura, Alfarius Eko Nugroho, Yusuke Hirasawa Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-12 09:47:29














»Ø¸´´ËÂ¥