| ²é¿´: 342 | »Ø¸´: 1 | ||
lizhaoyun½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú¸ö΢Æ×£¬¸ø10½ð
|
|
13C NMR (101 MHz, CDCl3) ¦Ä. 54.16,55.96,71.68,85.89,108.59,114.27,118.98,132.89,145.23,146.71. |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸2110£¬»¯Ñ§Ñ§Ë¶310·Ö£¬±¾¿ÆÖصãË«·ÇÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸»ª¶«Àí¹¤085601²ÄÁϹ¤³Ì303·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
»¯Ñ§0703-Ò»Ö¾Ô¸211-338·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
0703»¯Ñ§
ÒѾÓÐ27È˻ظ´
µ÷¼Á
ÒѾÓÐ6È˻ظ´
280Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
324Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
»¯Ñ§µ÷¼ÁÇóÖú
ÒѾÓÐ13È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½¨ÒéȺÖ÷¿ªÒ»¸ö΢Æ×ÇóÖúרÀ¸°É
ÒѾÓÐ14È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý,ǰ10¸ö¼´¿É
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ£¡¼±Çó£¡
ÒѾÓÐ6È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻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¡¿Î¢·´-É«Æ× ÔõôʹÓ𡣿
ÒѾÓÐ8È˻ظ´
10½ð±ÒÇóÖú΢ÉúÎïѧͨ±¨µÄÖÕÉóʱ¼ä
ÒѾÓÐ12È˻ظ´

wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lizhaoyun: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-09 17:51:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lizhaoyun: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-09 17:51:38
|
1 . rel-(3R,3'S,4R,4'S)-3,3',4,4'-Tetrahydro-6,6'-dimethoxy[3,3'-bi-2H-benzopyran]-4,4'-diol C20H22O6 ÏàËÆ¶È:100% Helvetica Chimica Acta 2000 Vol. 83 3344 Chemical Constituents of Tripterygium wilfordii Guangzhong Yang, Xueqiang Yin, and Yuanchao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . bisbenzopyran C20H22O6 ÏàËÆ¶È:100% Planta Medica 1997 63 454-456 A New Bisbenzopyran from Aloe barbadensis Roots Rubeeria Saleem, Shaheen Faizi, Farhat Deeba, Bina Shaheen Siddiqui, and Mahmood Husain Qazi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . d-pinoresinol ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 1996 31 524-529 STUDIES ON CHEMICAL CONSTITUENTS OF ROOTS OF EUPHORBIA PEKINENSIS LY Kong and ZD Min Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . pinoresinol C20H22O6 ÏàËÆ¶È:100% Natural Product Research 2002 16 359-363 Pinoresinol from Ipomoea Cairica Cell Cultures Csilla P¨¢ska; Gabbriella Innocenti; Mariagrazia Ferlin; M¨®nika Kunv¨¢ri; Mikl¨®s L¨¢szl¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-pinoresinol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2000 25 541-543 Studies on Chemical Constituents of Ligustrum obtusifolium Sieb. et Zucc. ZHOU Lixin, DING Yi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . pinoresinol C20H22O6 ÏàËÆ¶È:100% Fitoterapia 2003 74 184-187 Bioactive constituents of Leptadenia arborea A.El-Hassan , M.El-Sayed , A.I. Hamed , I.K. Rheeb,A.A. Ahmed, K.P. Zeller, R. Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pinoresinol C20H22O6 ÏàËÆ¶È:100% Fitoterapia 2001 72 80-82 Lignans from Strophanthus gratus S. Cowan, M. Stewart, D.K. Abbiw, Z. Latif ,S.D. Sarker,U, R.J. Nash Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (¡À) pinoresinol ÏàËÆ¶È:100% Phytochemistry 2000 54 897-899 Spectral comparisons of coniferyl and cinnamyl alcohol epoxide derivatives with a purported cis-epoxyconiferyl alcohol isolate Nathan R. Guz, Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)pinoresinol ÏàËÆ¶È:100% Phytochemistry 1998 49 1299-1304 Antialgal compounds from zantedeschia aethiopica Marina Della Grec¦Á, Maria Ferrar¦Á, Antonio Fiorentino, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . pleionin C20H22O6 ÏàËÆ¶È:100% Phytochemistry 1997 44 341-343 Lignans and a bichroman from Pleione bulbocodioides Li Bai, Masae Yamaki, Shuzo Takagi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Epoxyconiferyl alcohol C10H18O4 ÏàËÆ¶È:100% Phytochemistry 1995 38 801-802 Epoxyconiferyl alcohol from Fraxinus oxycarpa bark Ivanka Kostova, Dragomir Dinchev, Bozhana Mikhova, Tanya Iossifova Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . dehydro-diconiferylalcohol C20H22O6 ÏàËÆ¶È:100% Phytochemistry 1991 30 3087-3089 Synthesis of biologically active tetrahydro-furofuranlignan-(syringin, pinoresinol)- mono- and bis-glucosides Barbara Vermes, Otto Seligmann, Hildebert Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . pinoresinol ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 2005 36(2) 145-150 Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino Lee, Jong-Hwa; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,3'-bis(3,4-dihydro-4-hydroxy-6-methoxy-2H-1-benzopyran) C20H22O6 ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 2001 32(4) 302-306 Chemical Components from the Stem Barks of Kalopanax septemlobus Hong, Sung-Su; Han, Doo-Il; Hwang, Bang-Yeon; Choi, Woo-Hoi; Kang, Ho-Sang; Lee, Myung-Koo; Lee, Don-Koo; Lee, Kyong-Soon; Ro, Jai-Seup Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (+)-pinoresinol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2010 35 1261-1271 Chemical constituents of stems and branches of Adina polycephala ZHANG Yanling; GAN Maoluo; LI Shuai; WANG Sujuan; ZHU Chenggen; YANG Yongchun; HU Jinfeng; CHEN Naihong; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . pinoresinol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2010 35 2285-2288 Alkaloids and lignans from stems of Piper betle HUANG Xiangzhong; YIN Yan; HUANG Wenquan; SUN Kuizong; CHENG Chunmei; BAI Lian; DAI Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Compound 5 ÏàËÆ¶È:100% Bioorganic & Medicinal Chemistry 2008 16 2645-2650 Low molecular weight lignin suppresses activation of NF-¦ÊB and HIV-1 promoter Shinya Mitsuhashi, Takao Kishimoto, Yasumitsu Uraki, Takashi Okamoto, Makoto Ubukata Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . pinoresinol ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2006 37 672-673 °×Âí¹ÇÒ¶µÄ»¯Ñ§³É·ÖÑо¿ ÕÅÇ¿;Ëï¡Èå Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-pinoresinol C20H22O6 ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2003 1 79-81 Studies on the Chemical Constituents of Fraxinus chinensis Roxb. ZHANG Dong Mei; HU Li Hong; YE Wen Cai; ZHAO Shou Xun Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (− -pinoresinol C22H22O6 ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2008 6 411-414 Chemical Constituents from Daphne koreana Nakai HU Xiao-Jia,JIN Hui-Zi,SU Juan,ZHANG Wei,XU Wen-Zheng,YAN Shi-Kai,LIU Run-Hui,LÜ Hui-Zi,ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . pinoersinol C20H22O6 ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2010 8 414-418 Triterpenoids from the Fruits of Forsythia suspensa XUE Jiao; XIE Li; LIU Bao-Rui; YU Li-Xia Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . clemaphenolA C20H22O6 ÏàËÆ¶È:100% Acta Botanica Yunnanica 2010 32 455-462 A New Lignan from Elaeagnus lanceolata (Elaeagnaceae) SONG We i-Wu, LIBo, LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-09 15:30:49














»Ø¸´´ËÂ¥
-pinoresinol