| ²é¿´: 219 | »Ø¸´: 1 | ||
rootulyssesгæ (СÓÐÃûÆø)
|
[ÇóÖú]
Çóһ΢Æ×Êý¾Ý
|
|
΢Æ×Êý¾ÝÇóÖú 54.61,57.39,61.74,70.53,72.67,74.90,76.95,77.46,86.63,104.36,105.00,134.70,139.06,153.79 ÈܼÁ CD3OD |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
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´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ6È˻ظ´
СµÜ´ÓÖ²ÎïÖзÖÀë³öÒ»µ¥Ì廯ºÏÎÆä̼Æ×ÈçÏ£¬ÇóÆä΢Æ×Êý¾Ý£¬Íû¸ßÈËÏàÖú¡£
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÒ»¸öÉúÎï¼î»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
Çó²é΢Æ×Êý¾Ý Ò»»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
Çó²éÒ»¸ö»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿¸ß½ðÎÊÒ»×é̼Æ×Êý¾ÝµÄĸºË½á¹¹¡£
ÒѾÓÐ10È˻ظ´
yaolan123
½û³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 183 (¸ßÖÐÉú)
- ¹ó±ö: 0.255
- ½ð±Ò: 15027.2
- É¢½ð: 2847
- ºì»¨: 173
- ɳ·¢: 3
- Ìû×Ó: 3217
- ÔÚÏß: 486.8Сʱ
- ³æºÅ: 1352788
- ×¢²á: 2011-07-21
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
rootulysses: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-05-30 08:54:39
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
rootulysses: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-05-30 08:54:39
|
ѯ½á¹û£º¹²²éµ½463¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . liriodendrin ÏàËÆ¶È:92.8% Helvetica Chimica Acta 1981 64 3-15 New Iridoid Glucosides and a Lignan Diglucoside from Globularia alypumL Ratan K. Chaudhuri, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . liriodendrin ÏàËÆ¶È:92.8% Natural Product Sciences 2009 15 17-21 Lignans from the Roots of Berberis amurensis Park, Hyun-Bong; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Il-Kyun; Noh, Hyung-Jun; Choi, Sang-Un; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Acanthoside D ÏàËÆ¶È:92.8% Korean Journal of Pharmacognosy 2001 32(4) 316-321 Isolation and Quantitative Analysis of Acanthoside D from Acanthopanacis Cortex Hong, Sung-Su; Hwang, Ji-Sang; Lee, Seon-A; Hwang, Bang-Yeon; Ha, Kwan-Won; Ze, Keum-Ryon; Seung, Rack-Seun; Ro, Jai-Seup; Lee, Kyong-Soon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . liriodendrin ÏàËÆ¶È:92.8% Chinese Traditional and Herbal Drugs 1994 25 451-452+502 Studies on the Chemical Constituents of the Fresh Inflorescences of Desertliving Cistanche(Cistanche deserticola) Tu Pengfei; He Yanping and Lou Zhicen (Department of Pharmacognosy; Beijing Medical University; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . eleutherosides E ÏàËÆ¶È:92.8% Archives of Pharmacal Research 2004 27 106-110 Anti-oxidant activities ofacanthopanax senticosus stems and their lignan components Sanghyun Lee, Dongwook Son, Jiyoung Ryu, Yeon Sil Lee and Sang Hoon Jung, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . liriodendrin ÏàËÆ¶È:92.8% Natural Product Research and Development 1997 9(2) 7-10 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE CULTIVATED DESERTLIVING CISTANCHE (CISTANCHE DESERTICOLA) Tu Pengfei; He Yanping and Lou Zhicen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . liriodendrin C34H46O18 ÏàËÆ¶È:85.7% Acta Botanica Yunnanica 2001 23(1) 115-120 Phytochemical and Chemotaxonomic Studies on Liriodendron chinense and Paramichelia baillonii(Magnoliaceae) LI Shi-Sheng,TAN Ning-Hua,ZHOU Jun,ZHAO Shou-Xun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . liriodendrin ÏàËÆ¶È:85.7% China Journal of Chinese Materia Medica 2010 35 718-721 Chemical constituents from flowers of Chrysanthemum indicum WANG Jinyue; CHEN Dong; LIANG Lijuan; XUE Peifeng; TU Pengfei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . syringaresino-4,4'-di-O-¦Â-D-glucopyranside ÏàËÆ¶È:85.7% Chinese Journal of Medicinal Chemistry 1992 2(3) 56-60 STUDIES ON THE CHEMICAL CONSTITUENTS OF MORUS MONGOLICA(I) Yu Shunting Gu Lihong Pei Yuping Feng Jinsong Li Hongmei Chen Yingjie Nomura T Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . liriodendrin ÏàËÆ¶È:85.7% Turkish Journal of Chemistry 2009 33 561-568 A novel naphthoquinone glycoside from Rubia peregrina L. UFUK ÖZGEN, CAVİT KAZAZ, HASAN SEÇEN, İHSAN ÇALIŞ, MAKSUT COŞKUN, PETER J. HOUGHTON Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . liriodendrin ÏàËÆ¶È:85.7% Turkish Journal of Chemistry 2004 28 767-774 Secondary Metabolites from Phlomis kotschyana Ü. ŞEBNEM HARPUT, İCLAL SARACOĞLU, İHSAN ÇALIŞ, ALİ ARSLAN DÖNMEZ, AKITO NAGATSU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Syringaresinol-4,4'-di-O-¦Â-D-glucoside C34H46O18 ÏàËÆ¶È:85.7% Natural Product Research and Development 2012 24 298-302 Vasorelaxant Effect on Isolated Rabbit Aortic Rings and Chemical Constituents of n-Butanol Fraction from Leaves of Magnolia officinalis Rehd et Wils. YANG Zhu-ya; WEI Ying-fang; ZHOU Zhi-hong; LONG Fei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . syringin C17H24O9 ÏàËÆ¶È:78.5% Natural Product Sciences 2002 8 23-25 Studies on the Constituents of the Stem Barks of Acanthopanax gracilistylus W. W. Smith Liu, Xiang Qian; Chang, Seung-Yeup; Park, Sang-Yong; Nohara, Toshihiro; Yook, Chang-Soo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . liriodendrin ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2007 38 995-997 붬Çà¸ùÖл¯Ñ§³É·ÖµÄÑо¿ ÒüÎÄÇå;ÖÜÖÐÁ÷;×Þ½ÚÃ÷;ÃϽÜ;¸µ´ºÑà Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3,5-Dimethoxy-benzyl alcohol 4-O-¦Â-D-glucopyranoside C15H22O9 ÏàËÆ¶È:78.5% Archives of Pharmacal Research 2006 29 1086-1090 Cytotoxic phenolic constituents of Acer tegmentosum maxim Ki Myun Park, Min Cheol Yang, Kyu Ha Lee, Kyung Ran Kim and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . syringaresinol-4',4''-O-bis-¦Â-D-glucoside ÏàËÆ¶È:78.5% Chinese Pharmaceutical Journal 2007 42 339-348 Studies on Lignan Components of Asparagus officinalis HUANG Xue-feng, LUO Jun, ZHANG Yong, KONG Ling-yi* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . liriodendrin ÏàËÆ¶È:78.5% Lishizhen Medicine and Materia Medica Research 2009 20 2923-2925 Chemical Constituents from the Roots of Ilex pubescens WU Ting; ZHANG Xiao-qi; WANG Ying; YE Wen-cai; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 4-ôǼ׻ù-2,6-¼×Ñõ»ù±½·Ó-1-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:78.5% China Journal of Chinese Materia Medica 2012 37 1782-1787 Phenolic components from Petasites tricholobus ZHANG Yong; GUO Fujiang; ZENG Peng; JIA Qi; LI Yiming; ZHU Weiliang; CHEN Kaixian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 2-(methoxy)-2-(3,5-dimethoxy 4-hydroxyphenyl)-ethane-1,2-diol 1-O-¦Â-D-glucopyranoside C17H26O10 ÏàËÆ¶È:76.4% Natural Product Communications 2011 6 205-208 Secondary Metabolites from the Roots of Paronychia chionaea Sibel Avunduk, Özgen Alankuş-Çalişkan, Tomofumi Miyamoto, Chiaki Tanaka and Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . liriodendrin ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2005 40 653-656 Study on the chemical constituents of Linaria vulgaris HUA Hui-ming, LI Xian, XING Su-e, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . juniperoside C18H26O9 ÏàËÆ¶È:73.3% Planta Medica 1996 62 88-89 Phenyipropane Glycosides from Jun iperus pharnicea Glues C'omte, AlbertJ. Ghulia. Joseph Vercauteren,and Daovy P. Allais Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . syringiaresinol digloside ÏàËÆ¶È:73.3% Natural Product Research and Development 2008 20 52-55 Chemical Constituents of Debregeasia orientalis XIAO Yan-hua;CAO Hui; ZHANG Guo-lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . syringin ÏàËÆ¶È:71.4% Helvetica Chimica Acta 1981 64 3-15 New Iridoid Glucosides and a Lignan Diglucoside from Globularia alypumL Ratan K. Chaudhuri, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . syringin ÏàËÆ¶È:71.4% China Journal of Chinese Materia Medica 2009 34 2063-2066 Chemical constituents from leaves of A lbizia chinensis LIU Rui, YU Shishan, PEI Yuehu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . syringin ÏàËÆ¶È:71.4% China Journal of Chinese Materia Medica 2008 33 1641-1643 Study on Chemical Constituents from Juniperus sabina L. ZHAO Jun, YAN Ming, HUANG Yi, LIU Tao, ZHAO Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . syringin ÏàËÆ¶È:71.4% China Journal of Chinese Materia Medica 2006 31 1869-1872 Studies on chemical constituents of Acroptilon repens ZHAO Dongbao, ZHANG Wei, Li Mingjing, LIU Xiuhua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . liriodendrin ÏàËÆ¶È:71.4% Korean Journal of Pharmacognosy 1995 26(2) 122-129 Chemical Constituents and Biological Activity of Kalopanacis Cortex Lee, Eun; Choi, Moo-Young; Park, Hee-Juhn; Cha, Bae-Chun; Cho, Soon-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . (+)-(7S,8S)-syringylglycero-8-O-¦Â-D-glucopyranoside ÏàËÆ¶È:71.4% China Journal of Chinese Materia Medica 2010 35 456-467 Constituents from a water-soluble portion of ethanolic extract of Iodes cirrhosa GAN Maoluo; ZHU Chenggen; ZHANG Yanling; ZI Jiachen; SONG Weixia; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . [4-(1',2'-epoxy-3'-hydroxypropyl)-2,6-dimethoxyphenyl]-O-¦Â-D-glucopyranoside C17H24O10 ÏàËÆ¶È:71.4% Heterocycles 2003 60 1645-1652 Chemical Constituents of the Stem of Sargentodoxa cuneata Amooru G. Damu, Ping-Chung Kuo, Li-Shian Shi, Chang-Qi Hu, and Tian-Shung Wu* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 4-Ï©±û»ù-2,6-¶þ¼×Ñõ»ù±½»ùÆÏÌÑÌÇÜÕ C17H24O8 ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2009 40 1873-1876 ÌúƤʯõú»¯Ñ§³É·ÖµÄÑо¿ ¹Ü»Ý¾ê;ÕÅÑ©;ÍÀ·ï¾ê;Ò¦ÐÂÉú Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-05-30 08:15:55














»Ø¸´´ËÂ¥