| ²é¿´: 355 | »Ø¸´: 1 | ||
ligk½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| CÆ×Êý¾Ý£º61.51,79.10,79.13,79.76,99.41,103.18,103.96,116.55,121.75,128.15,128.80,149.92,156.66,157.50,161.70,164.03,182.37. |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ligk: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-09 20:14:41
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ligk: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-09 20:14:41
|
1 . 5,7,4'-Trihydroxy-8-methoxyflavone C16H12O6 ÏàËÆ¶È:82.3% Chemistry of Natural Compounds 2002 38 358-406 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:82.3% Journal of Shenyang Pharmaceutical University 2010 27 37-39 Isolation and identification of flavonoidal constituents from the leaves of Lonicera japonica Thunb. MA Jun-li, LI Ning, LI Xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5,7,4'-Trihydroxy-8-methoxyflavone ÏàËÆ¶È:82.3% Journal of Shenyang Pharmaceutical University 2003 20 181-183 Isolation and identif ication of the chemical constituents of roots of Scutellaria amoena C. H. Wright XIAO Li-he, WANG Hong-yan, SONG Shao-jiang, ZHANG Guang-ping, SONG Hai-xiu, XU Sui-xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:82.3% Journal of Shenyang Pharmaceutical University 2003 20 181-183 Isolation and identif ication of the chemical constituents of roots of Scutellaria amoena C. H. Wright XIAO Li-he, WANG Hong-yan, SONG Shao-jiang, ZHANG Guang-ping, SONG Hai-xiu, XU Sui-xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:82.3% Natural Product Research and Development 2003 15 405-406 CHEMICAL CONSITITUENTS OF PRANA DISCIFERA YU Rong; XU Qing; LI Bo-Gang; ZHANG Guo-Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:76.4% Journal of Shenyang Pharmaceutical University 2011 28 182-185 Isolation and identification of flavonoids of whole plant of Scutellaria barbata D. Don HE Shu-heng, ZHANG Yi, GE Dan-dan, WANG Tao, HU Li-min, GAO Xiu-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:76.4% Journal of Shenyang Pharmaceutical University 2003 20 339-348 Studies on chemical constituents of the roots of Scutellaria viscidula Bge. WANG Hong-yan, XIAO Li-he, LIU Li, XU Sui-xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,7,4'-trihydroxy-8-methoxyflavone ÏàËÆ¶È:76.4% Chemistry & Biodiversity 2012 9 2096-2158 Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3',3'''-biapigenin ÏàËÆ¶È:70.5% Phytochemistry 1993 34 295-296 Biflavonoids from the moss Homalothecium lutescens Tassilo Seeger, Hans Geiger, Hans Dietmar Zinsmeister, Wolfgang Rozdzinski Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . galangustin ÏàËÆ¶È:70.5% Bulletin des Soci¨¦t¨¦s Chimiques Belges 1983 92 497-498 Additional Proof for the Structure of the New Flavone Galangustin (Bucegin) Obtained by 13C-NMR Spectroscopy R. A. Dommisse and G. Savona Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ɽÄÎËØ-4'-¼×ÃÑ ÏàËÆ¶È:70.5% Journal of Tropical and Subtropical Botany 2000 8 182-184 ºì¶¹É¼(Taxus chinensis(Pilger) Rehd.)ÖеķÇ×ÏɼÍéÀ໯ºÏÎï ¹ÙÖÇ, ËÕ¾µÓé, ÔøÂ¤Ã·, Àîºì Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . apigenin ÏàËÆ¶È:70.5% Periodical of Ocean University of China 2013 43 077-080 Studies on Chemical Constitutents of Scutellaria barbata D.Don LI Yuan-Yuan, TANG Xu-Li, LI Ping-Lin, LI Guo-Qiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Onopordin C16H12O7 ÏàËÆ¶È:70.5% Zeitschrift f¨¹r Naturforschung C 1995 50 588-590 External Flavonoids of Three Species of Viguiera, Section Hypargyrea (Asteraceae) Eckhard Wollenweber, Marion Dörr, James N. Roitman and Edward Schilling Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . hypolaetin-8,3'-diMe ÏàËÆ¶È:70.5% Zeitschrift f¨¹r Naturforschung C 1997 52 301-307 Exudate Flavonoids in Asteraceae from Arizona, California and Mexico* Eckhard Wollenweber, Marion Dörr, Hannelore Fritz, Sabine Papendieck,G. Yatskievych and James N. Roitman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . apigenin ÏàËÆ¶È:64.7% Planta Medica 1987 53 216-217 Biflavonoids in Hypericum perforatum1; Part 1. Isolation of 13, 118-Biapigenin R. Berghofer, J. Holzl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . apigenin ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 1981 29 254-256 Studies on a Novel p-Coumaroyl Glucoside of Apigenin and on Other Flavonoids isolated from Patchouli (Labiatae) HIDEJI ITOKAWA,KEIICHI SUTO and KOICHI TAKEYA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 5,7-dihydroxy-8,2'-dimethoxyflavone C17H14O6 ÏàËÆ¶È:64.7% Chemistry of Natural Compounds 2002 38 358-406 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Scutevulin C16H12O6 ÏàËÆ¶È:64.7% Chemistry of Natural Compounds 2002 38 358-406 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . apigenin ÏàËÆ¶È:64.7% Acta Botanica Boreali-Occidentalia Sinica 2008 28 1246-1249 Chemical Constituents in the Leaves of Alsophila spinulosa CHEN Feng-zheng, XIANG Qing-xiang, LI Shu-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 4¡ä-Methoxyisoscutellargin ÏàËÆ¶È:64.7% Molecules 2003 8 614-621 Constituents from Moghat, the Roots of Glossostemon bruguieri (Desf.) Meselhy R. Meselhy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . Apigenin ÏàËÆ¶È:64.7% Molecules 2003 8 614-621 Constituents from Moghat, the Roots of Glossostemon bruguieri (Desf.) Meselhy R. Meselhy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . Apigenin ÏàËÆ¶È:64.7% Journal of Chinese Pharmaceutical Sciences 1997 6 07 Flavonoids from Speranskia Tuberculata Yan-Mei Li, Yu-Yin gZhao, Yun-Bai Fan, Xuan Wang and Li-Ning Cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . apigenin ÏàËÆ¶È:64.7% Journal of Chinese Pharmaceutical Sciences 2000 9 134-136 Two Novel Flavonoids from Ixeris sonchifolia Feng Xizhi, Xu Suixu and Dong Mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . apigenin ÏàËÆ¶È:64.7% China Journal of Chinese Materia Medica 2009 34 3043-3046 Chemical constituents in Buddleja albiflora TAO Liang, HUANG Jincheng, ZHAO Yanping, LI Chong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-08 20:39:03














»Ø¸´´ËÂ¥