| ²é¿´: 617 | »Ø¸´: 1 | |||
fanqingfeiľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×Êý¾Ý²éѯÇóÖú£¬¡µ70% ÒÑÓÐ1È˲ÎÓë
|
| ¦Ä C (151 MHz, DMSO) 17.86, 42.05, 42.29, 55.66, 66.09, 68.34, 69.57, 70.27, 70.68, 70.71, 72.05, 72.98, 75.50, 76.26, 78.39, 78.46, 95.53, 95.58, 96.36, 99.35, 100.62, 103.33,112.06, 111.98, 114.08, 114.15, 117.79, 117.98, 130.88, 130.96, 146.42, 146.44, 147.91, 147.96, 162.51, 162.55, 163.01, 163.05, 165.08, 165.13, 197.09, 216.88. |
» ²ÂÄãϲ»¶
296Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
333Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
²ÄÁÏר˶ 335 ·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
07»¯Ñ§303Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±±¿Æ281ѧ˶²ÄÁÏÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
289Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
ÍøÂç¿Õ¼ä°²È«0839Õе÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏ277Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
274Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085600 ²ÄÁÏÓ뻯¹¤ 329·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
άÆ×Êý¾Ý²éѯÇóÖú£¬¡µ70%
ÒѾÓÐ4È˻ظ´
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý gf
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý,ǰ10¸ö¼´¿É
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48104.9
- ºì»¨: 52
- Ìû×Ó: 6735
- 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
fanqingfei: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-10 15:57:52
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fanqingfei: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-10 15:57:52
|
1 . (¡À)-eriodictyol 7-O-¦Â-D-glucuronide C21H20O12 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1990 38 3218-3225 Constituents of a Fern, Davallia mariesii MOORE. I. Isolation and Structures of Davallialactone and a New Flavanone Glucuronide Cheng-Bin CUI,Yasuhiro TEZUKA,Tohru KIKUCHI,Hirofumi NAKANO,Tatsuya TAMAOKI and Jong-Hee PARK Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . hesperidin ÏàËÆ¶È:64.2% Phytochemistry 1977 16 1110-1112 A 13C-NMR study of the structure of an acyl-linarin from Valeriana wallichii Vedantha Mohan Chari, Madelon Jordan, Hildebert Wagner, Peter W. Thies Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . prainianonide C22H22O11 ÏàËÆ¶È:57.1% Canadian Journal of Chemistry 2011 89 461¨C464 Flavanone glucuronides from the leaves of Garcinia prainiana Saranyoo Klaiklay, Yaowapa Sukpondma, Vatcharin Rukachaisirikul, Nongporn Hutadilok-Towatana, and Kanokphorn Chareonrat Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . scrophuloside B4 C42H48O18 ÏàËÆ¶È:54.7% Phytochemistry 2005 66 1186-1191 A sugar ester and an iridoid glycoside from Scrophularia ningpoensis Anh-Tho Nguyen, Jeanine Fontaine, Hugues Malonne, Magda Claeys,Michel Luhmer, Pierre Duez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . scrophuloside B4 ÏàËÆ¶È:54.7% Biochemical Systematics and Ecology 2011 39 902-905 Acylated iridoid glycosides from Scrophularia saharae Batt. & Trab. Rachid Chebaki, Hamada Haba, Christophe Long, Laurence Marcourt, Mohammed Benkhaled Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Scrophuloside A4 C43H50O19 ÏàËÆ¶È:54.7% Chemical & Pharmaceutical Bulletin 2007 55 159-222 Naturally Occurring Iridoids. A Review, Part 1 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Scrophuloside B4 [6-O-(2''-O-Acetyl-3''-O-cinnamoyl-4''-O-p-methoxycinnamoyl-¦Á-L-rhamnopyranosyl)catalpol] C42H48O18 ÏàËÆ¶È:54.7% Chemical & Pharmaceutical Bulletin 2007 55 159-222 Naturally Occurring Iridoids. A Review, Part 1 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . delphinidin 3-[6-O-(¦Á-rhamnopyranosyl)-¦Â-glucopyranoside]-7-O-[6-O-(4-O-(¦Â-glucopyranosyl)-p-hydroxybenzoyl)-¦Â-glucopyranoside] C53H58O30 ÏàËÆ¶È:54.3% Heterocycles 2009 77 401-408 7-Acylated Anthocyanins with p-Hydroxybenzoic Acid in the Flowers of Campanula medium Kenjiro Toki, Norio Saito, Hiroyuki Nishi, Fumi Tatsuzawa, Atsushi Shigihara, and Toshio Honda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Kaempferol-3-O-{[¦Â-D-xylopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú6)][¦Á-L-rhamnopyranosyl(1¡ú2)]}-¦Â-D-3-trans-p-coumaroylgalactopyranoside C47H54O25 ÏàËÆ¶È:53.4% Chemical & Pharmaceutical Bulletin 2002 50(7) 981-984 New Flavonol Tetraglycosides from Astragalus caprinus Nabil SEMMAR,Bernard FENET,Katia GLUCHOFF-FIASSON,Gilles COMTE,and Maurice JAY Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . scrophuloside A4 C43H50O19 ÏàËÆ¶È:53.4% Journal of Natural Products 1999 62 1079-1084 Acylated Iridoid and Phenylethanoid Glycosides from the Aerial Parts of Scrophularia nodosa Toshio Miyase and Ai Mimatsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . helicioside B C21H22O12 ÏàËÆ¶È:52.3% Phytochemistry 2006 67 2681-2685 5-O-glucosyldihydroflavones from the leaves of Helicia cochinchinensis Ken-Ichi Morimura, Asuka Gatayama, Reiki Tsukimata, Katsuyoshi Matsunami,Hideaki Otsuka, Eiji Hirata, Takakazu Shinzato, Mitsunori Aramoto,Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . MF-1a ÏàËÆ¶È:52.3% Phytochemistry 2003 589-595 A ¡°flavone-polysaccharide¡± redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides Kenneth R. Markham Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . MF-1b ÏàËÆ¶È:52.3% Phytochemistry 2003 589-595 A ¡°flavone-polysaccharide¡± redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides Kenneth R. Markham Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 2''',3'''-diacetyl-O-betonyoside D C40H52O21 ÏàËÆ¶È:52.3% Chinese Chemical Letters 2007 18 155-157 Two new phenylethanoid glycosides from the roots of Phlomis umbrosa Pu Liu, Yoshihisa Takaishi, Hong Quan Duan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2''', 3'''-di-acetyl-O-betonyoside D C40H52O21 ÏàËÆ¶È:52.3% Journal of Asian Natural Products Research 2009 11 69-74 Phenylethanoid glycosides from the roots of Phlomis umbrosa Pu Liua, Rui-Xue Denga, Hong-Quan Duanb, Wei-Ping Yina and Tian-Zeng Zhaoc Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Cistansinensose A1/A2 C27H38O17 ÏàËÆ¶È:52.3% Journal of Asian Natural Products Research 2007 9 79-84 Chemical constituents of Cistanche sinensis P.-F. TU, H.-M. SHI, Z.-H. SONG, Y. JIANG and Y.-Y. ZHAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 6-O-¦Á-L-rhamnopyranosylcatalpol C31H40O17 ÏàËÆ¶È:52.3% Phytochemistry 1991 30 1917-1920 Iridoid diglycoside monoacyl esters from stems of Premna japonica Hideaki Otsuka, Naoko Kubo, Yukari Sasaki, Kazuo Yamasaki, Yoshio Takeda, Tarow Seki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-02-09 19:37:14













»Ø¸´´ËÂ¥
6