| ²é¿´: 404 | »Ø¸´: 2 | |||
nina_326гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÔÚÏßµÈ ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï1£º 13C NMR (101 MHz, MeOD) 62.52, 66.78, 71.12, 75.02, 77.17, 78.34, 82.40, 94.71, 99.89, 100.99, 105.48, 116.18, 117.46, 123.54, 135.26, 146.16, 149.84, 158.51, 163.24, 165.98, 179.70 »¯ºÏÎï2£º 13C NMR (101 MHz, MeOD) 62.83, 68.32, 69.77, 71.34, 71.73, 75.00, 75.32, 77.75, 78.08, 102.80, 104.71, 108.22, 111.82, 129.39, 129.39, 129.68, 129.68, 134.53, 137.52, 158.35, 160.10, 170.17 |
» ²ÂÄãϲ»¶
269Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
267Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ6È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ10È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ31È˻ظ´
Ò»Ö¾Ô¸211 0703»¯Ñ§ 346·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл~
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú £¡£¡£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡ÔÚÏߵȰïæ£¡
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡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
nina_326: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 16:39:48
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
nina_326: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 16:39:48
|
1 . isoquercitrin ÏàËÆ¶È:85.7% Chemical & Pharmaceutical Bulletin 2001 49(8) 1039-1041 Phlomisflavosides A and B, New Flavonol Bisglycosides from Phlomis spinidens Yoshio TAKEDA,Natsuko ISAI, Toshiya MASUDA,Gisho HONDA, Yoshihisa TAKAISHI,Michiho ITO, Hideaki OTSUKA,Ozodbek A. ASHURMETOV, and Olimjon K. KHODZHIMATOV Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . quercetin 3-glucoside ÏàËÆ¶È:85.7% Phytochemistry 2003 229-237 Malonylated flavonol glycosides from the petals of Clitoria ternatea Kohei Kazuma, Naonobu Noda, Masahiko Suzuki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Quercetin-3-O-¦Â-D-glucopyranoside C21H20O12 ÏàËÆ¶È:85.7% Acta Botanica Yunnanica 2009 31(3) 284-288 Phenolic Constituents from the Fruits of Amomum tsao2ko (Zingiberaceae) WANGWei,YANG Chong-Ren,ZHANG Ying-Jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Quercetin-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:85.7% Acta Botanica Yunnanica 2000 22(3) 358-360 Flavonoids from Knema globularia MEI Wen-Li,YANG Yong,NI Wei,CHEN Chang-Xiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Quercitrin ÏàËÆ¶È:85.7% Journal of Chinese Pharmaceutical Sciences 2004 13 214-216 Flavonoids from Leaves of Heritiera littoralis D. TIAN Yan; WU Jun; and ZHANG Si Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Isoquercitrin ÏàËÆ¶È:85.7% Natural Product Sciences 2008 14 281-288 Chemical Constituents of Lathyrus davidii Park, Su-Yeon; Kim, Ju-Sun; Lee, So-Young; Bae, Ki-Hwan; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Hirsutrin C21H20O12 ÏàËÆ¶È:85.7% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 636-638 CHEMICAL CONSTITUENTS FROM THE STEM BARK OF Acer barbinerve Dong-Joo Kwon and Young-Soo Bae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . quercetin-3-O-¦Â-D-glucoside ÏàËÆ¶È:85.7% Asian Journal of Chemistry 2015 27(3) 991−994 Isolation and Identification of Flavonoids with Aldose Reductase Inhibitory Activity from Petasites japonicus DONG GU LEE, KI HO LEE, KWANG-WOO PARK, CHAN KYU HAN, BUOM-YONG RYU, EUN JU CHO and SANGHYUN LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . isoquercitrin ÏàËÆ¶È:85.7% China Journal of Chinese Materia Medica 2010 35 607-609 Chemical constituents in Flos Sophorae Carbonisatus LI Raorao*; WANG Caifang; LEI Peilin; HUANG Lanlan; YUAN Sitong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Isoquercitrin ÏàËÆ¶È:85.7% Phytochemical Analysis 2006 17 20-24 Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3-O-glycosides Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun and Akiyo Sakushima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-24 15:56:52
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
|
1 . 2-hydroxy-4-O-[¦Â-xylopyranosyl(1''¡ú6')-¦Â-glucopyranosyl]-benzoate C25H30O13 ÏàËÆ¶È:84% Journal of Asian Natural products Research 2010 12 70-75 New grayanol diterpenoid and new phenolic glucoside from the flowers of Pieris formosa Wei-Guang Wang; Hong-Mei Li; Hai-Zhou Li; Zhao-Yuan Wu; Rong-Tao Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Benzyl 2-hydroxy-6-methoxybenzoate 2-O-¦Â¨CD¨Cglucoside C21H24O9 ÏàËÆ¶È:81.8% Journal of Asian Natural Products Research 2007 9 603-607 New sesquiterpene and phenolic glucosides from Saussurea involucrata HONG-BING WANG, HUA-PING ZHANG, GUANG-MIN YAO, YU-BO WANG and GUO-WEI QIN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . benzyl 2-O-¦Â-D-glucopyranosyl-2,6-dihydroxybenzoate C20H22O9 ÏàËÆ¶È:72.7% Phytochemistry 2001 58 1073-1081 Potential allelochemicals from Sambucus nigra Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Lucio Previtera, Ana M. Simonet, Armando Zarrelli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . benzyl 2-O-¦Â-D-glucopyranosyl-2,6-dihydroxybenzoate ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2013 38 1378-1385 Chemical constituents from flower buds of Lonicera japonica WANG Fang, JIANG Yue-ping, WANG Xiao-liang, LIN Sheng, PU Peng-bin, ZHU Cheng-gen, WANG Su-juan, YANG Yong-chun, SHI Jian-gong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . foliachinenosides A2 C26H32O13 ÏàËÆ¶È:69.2% Heterocycles 2008 75 1435-1446 New Phenolic Glycosides from the Leaves of Salacia chinensis Seikou Nakamura, Yi Zhang, Tao Wang, Hisashi Matsuda, and Masayuki Yoshikawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 1 ÏàËÆ¶È:68.1% Phytochemistry 1990 29 1179-1181 Amygdalin acyl derivatives,cyanogenic glycosides from the seeds of Merremia dissecta Adolf Nahrstedt,Essam Abdel Sattar,Soheir M.H. El-Zalabani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Pieceid-(1¡ú6)-¦Â-D-glucopyranoside C26H32O13 ÏàËÆ¶È:66.6% Parasitology Research 2007 101 237-241 Antiplasmodial activity of novel stilbene derivatives isolated from Parthenocissus tricuspidata from South Korea Il Hong Son, Ill-Min Chung, Sun-Joo Lee, Hyung-In Moon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (E)-2,3,5,4'-tetrahydroxystilbene-2-O-(6''-O-¦Â-D-glucopyranosyl)-¦Â-D-glucopyranoside C26H32O14 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2013 15 1145-1151 Five new stilbene glycosides from the roots of Polygonum multiflorum Shuo-Guo Li, Li-Li Chen, Xiao-Jun Huang, Bing-Xin Zhao, Ying Wang & Wen-Cai Ye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Plicatumoside A C26H32O15 ÏàËÆ¶È:65.3% Journal of Natural Medicines 2011 65 202-205 Two new glycosides from Viburnum plicatum Thunb. ex Murray var. plicatum f. plicatum Masao Kikuchi ,Rie Onoguchi ,Yasunori Yaoita ,Koichi Machida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . benzyl 2-O-¦Â-apiofuranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-2,6-dihydroxybenzoate C25H30O13 ÏàËÆ¶È:65.2% Heterocycles 2010 80 477-488 Glycosides from Vallaris solanaceae with TRAIL-Resistance-Overcoming Activity Firoj Ahmed, Samir Kumar Sadhu, Takashi Ohtsuki, Amina Khatun, and Masami Ishibashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . benzyl-¦Á-L-arabinopyranosyl(1¡ú6)-¦Â-D-glucopyranoside C18H26O10 ÏàËÆ¶È:63.6% Phytochemistry 1996 42 1031-1034 Aliphatic and aromatic glycosides from the cell cultures of Lycopersicon esculentum Salvatore De Rosa, Alfonso De Giulio, Giuseppina Tommonaro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-03-24 16:20:35













»Ø¸´´ËÂ¥