| ²é¿´: 968 | »Ø¸´: 3 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
ai532521ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
|
ÈܼÁ£ºë®´ú¼×´¼ »¯Ñ§Î»ÒÆ£º20.6,47.0,51.6,55.6,55.6,56.0,63.5,63.9,100.7,107.2,111.7,112.0,115.3,115.5,119.6,120.5,135.3,135.5,141.6,144.5,144.6,147.2,147.6,147.7,157.8,170.0 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸Ìì½ò´óѧ»¯Ñ§¹¤ÒÕרҵ£¨081702£©315·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
290Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
²ÄÁÏÓ뻯¹¤Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
293Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
¹¤¿Æ²ÄÁÏ085601 279Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏר˶306Ó¢Ò»Êý¶þ
ÒѾÓÐ8È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶µ÷¼Á
ÒѾÓÐ5È˻ظ´
085600²ÄÁÏÓ뻯¹¤
ÒѾÓÐ4È˻ظ´
085601²ÄÁϹ¤³Ìר˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ìáǰлл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´
΢Æ×²é½á¹¹£¬ÓÐÆ×ͼ
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ai532521
ľ³æ (СÓÐÃûÆø)
- Ó¦Öú: 13 (СѧÉú)
- ½ð±Ò: 3044.6
- É¢½ð: 1000
- ºì»¨: 4
- Ìû×Ó: 281
- ÔÚÏß: 305.7Сʱ
- ³æºÅ: 1804477
- ×¢²á: 2012-05-08
- ÐÔ±ð: GG
- רҵ: ÖÐҩѧ
3Â¥2014-01-03 19:33:38
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
ai532521: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2014-01-03 18:31:53
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ai532521: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2014-01-03 18:31:53
|
²éѯ½á¹û£º¹²²éµ½124¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . gnetuhainin P ÏàËÆ¶È:61.5% Chinese Chemical Letters 2000 11 1061-1062 Gnetuhainin P, a New Isorhapontigenin Dimer from the Lianas of Gnetum hainanense Ying Hong WANG, Kai Sheng HUANG, Mao LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gnetuhainin P C30H28O9 ÏàËÆ¶È:61.5% Journal of Asian Natural Products Research 2001 3 169-176 Four New Stilbene Dimers from the Lianas of Gnetum Hainanense YING-ZIONG WANG, KAI-SHENG HUANG and MA0 LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . quebecol C24H26O7 ÏàËÆ¶È:61.5% Journal of Functional Foods 2011 3 125-128 Quebecol, a novel phenolic compound isolated from Canadian maple syrup Liya Li, Navindra P. Seeram Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . actifolin C22H24O7 ÏàËÆ¶È:57.6% Phytochemistry 1989 28 952-954 A lignan from Actinodaphne longifolia Hitoshi Tanaka,Takeshi Nakamura,Kazuhiko Ichino,Kazuo Ito Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (7R,8S,7'R,8'S)-4,9,4',9'-Tetrahydroxy-3,3'-dimethoxy-7,7'-epoxylignan 9-O-¦Â-D-Glucopyranoside C26H34O12 ÏàËÆ¶È:57.6% Helvetica Chimica Acta 2010 93 2164-2175 Four New Lignan Glycosides from Osmanthus fragransLour. var. aurantiacusMakino Koichi Machida, Megumi Yamauchi, Eriko Kurashina and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Hypericorin A C26H22O9 ÏàËÆ¶È:57.6% Planta Medica 2011 77 2013-2018 Anti-Inflammatory Xanthones from the Twigs of Hypericum oblongifolium Wall. Ali, Mumtaz; Arfan, Muhammad; Ahmad, Manzoor; Singh, Kuldip; Anis, Itrat; Ahmad, Habib; Choudhary, Muhammad Iqbal; Shah, Muhammad Raza: Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . lappaol B ÏàËÆ¶È:56.6% Acta Botanica Sinica 1998 40 466-469 Studies on the Lignans of Polygonum Orientale ZHENG Shang-Zhen, WANG Ding-Yong, MENG Jun-Cai, SHEN Xu-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . jacpaniculine C30H33NO9 ÏàËÆ¶È:56.6% Phytochemistry 1994 37 1637-1640 Jacpaniculines the first lignanamide alkaloids from the convolvulaceae Anke Henrici, Macki Kaloga, Eckart Eicht Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . bisisorhapontigenin E C30H26O8 ÏàËÆ¶È:56.6% Heterocycles 2006 68 983-991 Preparation of Bioactive Isorhapontigenin Dimers through Chemical Transformation of Bisisorhapontigenin A Chun-Suo Yao and Mao Lin* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4,4¡ä-dihydroxy-3,3¡ä-dimethoxy-9-butoxy-9,9¡ä-epoxylignan C24H32O6 ÏàËÆ¶È:53.8% Journal of Natural Products 2008 71(11) 1902-1905 Phenylpropanoids from Daphne feddei and Their Inhibitory Activities against NO Production Shuang Liang, Yun-Heng Shen, Jun-Mian Tian, Zhi-Jun Wu, Hui-Zi Jin, Wei-Dong Zhang, and Shi-Kai Yan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . gnetifolin F C25H24O7 ÏàËÆ¶È:53.8% Journal of Natural Products 2003 66 558-560 Phenolic Constituents of Gnetum klossii Zulfiqar Ali, Toshiyuki Tanaka, Ibrahim Iliya, Munekazu Iinuma, Miyuki Furusawa, Tetsuro Ito, Ken-ichi Nakaya, Jin Murata, and Dedy Darnaedi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . lactucaside 26H32O13 ÏàËÆ¶È:53.8% Journal of Natural Products 2003 66 625-629 Antidiabetic Dimeric Guianolides and a Lignan Glycoside from Lactuca indica Chia-Chung Hou, Shwu-Jiuan Lin, Juei-Tang Cheng, and Feng-Lin Hsu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 16 C33H46O11 ÏàËÆ¶È:53.8% Journal of Natural Products 2007 70 1588-1592 Enantioselective Synthesis of the Tetrahydrofuran Lignans (¨C)- and (+)-Magnolone Tomofumi Nakato and Satoshi Yamauchi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 15 C23H30O9 ÏàËÆ¶È:53.8% Journal of Natural Products 2007 70 1588-1592 Enantioselective Synthesis of the Tetrahydrofuran Lignans (¨C)- and (+)-Magnolone Tomofumi Nakato and Satoshi Yamauchi Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-acetoxymethyl-5-[(E)-3-acetoxypropen-1-yl)]-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydrobenzofuran ÏàËÆ¶È:53.8% Journal of Natural Products 1998 61 771-775 Lignans from Chilean Propolis Susanne Valcic, Gloria Montenegro, and Barbara N. Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (+)-lariciresinol 3-acetate C22H26O7 ÏàËÆ¶È:53.8% Journal of Natural Products 1998 61 1482-1490 Bisamides, Lignans, Triterpenes, and Insecticidal Cyclopentabenzofurans from Aglaia Species1 G. Brader, S. Vajrodaya, H. Greger, M. Bacher, H. Kalchhauser, and O. Hofer Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3'-methoxy-3,4-methylenedioxy-4',7-epoxy-9-nor-8,5'-neolignan-9'-acetoxy C21H20O6 ÏàËÆ¶È:53.8% Natural Product Research 2005 19 373-377 Antitrypanosomal activity of a novel norlignan purified from Nectandra lineata Lilia Ch¨¦rigo; Venancio Polanco; Eduardo Ortega-Barria; Maria V. Heller; Todd L. Capson; Luis Cubilla Rios Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . chestnutlignansoide C26H34O10 ÏàËÆ¶È:53.8% Acta Pharmaceutica Sinica 2004 Vol 39 531-533 A new lignan glycoside from the flower of Castanea mollissima Blume TANG Wen-zhao; DING Xing-bao; XIN Yi-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Okanin-4-methoxy-4'-O-(6''-O-acetyl-glucopyranoside) C24H26O12 ÏàËÆ¶È:53.8% Phytochemistry 1993 32 218-220 S.R. Rojatkar, B.A. Nagasampagi Karl Redl, Brent Davis, Rudolf Bauer Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (8S,7'S,8'S)-7-acetoxy-3,4-dimethoxy-3',4'-methylenedioxy-7 1-seco-6,7',8,8'-neolignan ÏàËÆ¶È:53.8% Phytochemistry 1990 29 1799-1810 Lignoids and arylalkanones from fruits of Virola elongata Massuo J. Kato,Massayoshi Yoshida,Otto R. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Compound 8 C23H31N6 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2009 19 6399-6403 Kristjan S. Gudmundsson, Sharon D. Boggs, John G. Catalano, Angilique Svolto, Andrew Spaltenstein, Michael Thomson, Pat Wheelan, Stephen Jenkinson Kristjan S. Gudmundsson, Sharon D. Boggs, John G. Catalano, Angilique Svolto, Andrew Spaltenstein, Michael Thomson, Pat Wheelan, Stephen Jenkinson Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-01-03 17:05:54
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
4Â¥2014-01-04 17:52:50













»Ø¸´´ËÂ¥