| ²é¿´: 203 | »Ø¸´: 1 | ||
Ëïæ¤æ¤ÊµÏ°°æÖ÷
|
[ÇóÖú]
ÇóÖú΢ÆÕÊý¾Ý
|
|
13CNMR(101MHz,DMSO) 39.52,61.43,61.76,68.62,69.90,70.03,71.14,73.90,78.39,79.16,80.40,80.74,85.42,85.63,99.20,106.56,115.52,127.39,129.23,135.33,158.27,178.43,195.52 ¼±Óã¡Ð»Ð»£¡£¡£¡ |
» ²ÂÄãϲ»¶
324·Ö 085600²ÄÁÏÓ뻯¹¤
ÒѾÓÐ14È˻ظ´
×Ü·Ö343£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ5È˻ظ´
262Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
302Çóµ÷¼ÁÒ»Ö¾Ô¸±±º½070300£¬±¾¿ÆÖ£´ó»¯Ñ§
ÒѾÓÐ9È˻ظ´
Ó¢Ò»ÊýÒ»408£¬×Ü·Ö284£¬¶þÕ½Õæ³ÏÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
289Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
309Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúάÆÕÊý¾Ý¿âÎÄÏ×һƪ
ÒѾÓÐ1È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹£¨¹²4¸ö£©
ÒѾÓÐ5È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢ÆÕÊý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢ÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆÕÕ˺ÅÃÜÂë
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÍƼöÒ»ÏÂÄÜ×ö΢²¨ºÏ³ÉµÄÆÕͨ΢²¨Â¯
ÒѾÓÐ8È˻ظ´
½Ì½ÌÎÒÈçºÎʹÓÃάÆÕ
ÒѾÓÐ8È˻ظ´
¡¾ÌÖÂÛ¡¿ÇóÖú£º£ºNOTEEXPRESS Ö±½ÓÁ¬ÏßάÆÕÊý¾Ý¿âÏÂÔØÈ«ÎÄ
ÒѾÓÐ3È˻ظ´
wq0616
³¬¼¶°æÖ÷
![]()
![]()
![]()
![]()
- Ó¦Öú: 323 (´óѧÉú)
- ½ð±Ò: 6659.6
- ºì»¨: 8
- Ìû×Ó: 955
- ÔÚÏß: 72.9Сʱ
- ³æºÅ: 2001721
- ×¢²á: 2012-09-14
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ëïæ¤æ¤: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-27 22:26:43
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ëïæ¤æ¤: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-27 22:26:43
|
1 . hydroxysafflor yellow A C27H32O16 ÏàËÆ¶È:88% Chemical & Pharmaceutical Bulletin 1993 41 1796-1802 Two New Quinochalcone Yellow Pigments from Carthamus tinctorius and Ca2+ Antagonistic Activity of Tinctormine Meselhy R. MESELHY,Shigetoshi KADOTA,Yasunori MOMOSE,Noboru HATAKEYAMA,Akihiko KUSAI,Masao HATTORI and Tsuneo NAMBA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Hydroxysafflor yellow A ÏàËÆ¶È:81.4% Journal of Natural Products 2013 76 270-274 NMR Solution Structure Study of the Representative Component Hydroxysafflor Yellow A and Other Quinochalcone C-Glycosides from Carthamus tinctorius Zi-Ming Feng, Jun He, Jian-Shuang Jiang, Zhong Chen, Ya-Nan Yang, and Pei-Cheng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . hydroxysafflor yellow A C27H32O16 ÏàËÆ¶È:77.7% Journal of Natural Products 1993 Vol 56 39 New Triterpenes and Flavonoids from the Leaves of Bosistoa brassii M. R. Meselhy, Shigetoshi Kadota, Masao Hattori, Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . safflor yellow A ÏàËÆ¶È:76% Chemical & Pharmaceutical Bulletin 1993 41 1796-1802 Two New Quinochalcone Yellow Pigments from Carthamus tinctorius and Ca2+ Antagonistic Activity of Tinctormine Meselhy R. MESELHY,Shigetoshi KADOTA,Yasunori MOMOSE,Noboru HATAKEYAMA,Akihiko KUSAI,Masao HATTORI and Tsuneo NAMBA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . safflor yellow A ÏàËÆ¶È:70.3% 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 ̼Æ×Ä£Äâͼ 6 . 5,7,4'-trihydroxy-8-C-¦Â-D-glucopyranosyl flavanone ÏàËÆ¶È:56.5% China Journal of Chinese Materia Medica 2008 33 1700-1702 Studies on flavonoid glycosides of Sarcandra glabra HUANG Mingju, ZENG Guangyao, TAN Jianbing, LI Yanlan, TAN Guishan, ZHOU Yingjun Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . aromadendrin 6-C-glucoside ÏàËÆ¶È:56.5% Korean Journal of Pharmacognosy 2004 35(1) 80-87 The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Epicatechin 4'-O-Sulfate ÏàËÆ¶È:56.5% Journal of Agricultural and Food Chemistry 2012 60 3592-3598 Characterization of Sulfated Quercetin and Epicatechin Metabolites Montserrat Dueñas, Susana Gonz¨¢lez-Manzano, Felipe Surco-Laos, Ana Gonz¨¢lez-Paramas, and Celestino Santos-Buelga Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2R,3R)-Aromadendrin-6-C-¦Â-D-glucopyranoside C21H22O11 ÏàËÆ¶È:56.5% Journal of Agricultural and Food Chemistry 2012 60 2053-2062 Isolation and Structure Elucidation of Highly Antioxidative 3,8¡å-Linked Biflavanones and Flavanone-C-glycosides from Garcinia buchananii Bark Timo D. Stark, Toshiaki Matsutomo, Sofie Lösch, Paul A. Boakye, Onesmo B. Balemba, Sofie P. Pasilis, and Thomas Hofmann Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-C-glucosylnalingenin ÏàËÆ¶È:52.1% Korean Journal of Pharmacognosy 1994 25(3) 199-203 Flavonoids from the Leaves of Betula platyphylla var. latifolia Lee, Min-Won Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Apigenin 6-C-¦Â-D-xylopyranosyl-8-C-¦Â-D-glucopyranoside ÏàËÆ¶È:52.1% Archives of Pharmacal Research 2007 30 161-166 Antioxidant flavone glycosides from the leaves of Sasa borealis Hae-Suk Park, Ju Hee Lim, Hyun Jung Kim, Hyun Jin Choi and Ik-Soo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . apigenin-6,8-di-C-¦Â-D-glucopyranoside and apigenin-6 ÏàËÆ¶È:52.1% Chinese Pharmaceutical Journal 2005 40 1457-1459 Study on flavonoids of Arisaema erubescens DU Shu-shan, LEI Ning, XU Yan-chun, WEI Lu-xue Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . HLB-1 ÏàËÆ¶È:52.1% Chinese Pharmaceutical Journal 2008 43 1457-1460 Effect of Flavonoid-C-Glycosides from Trigonella foenum-graecum on Hypoglycemic Activities in Alloxan-Induced Mice SHAN Jun-jie, REN Jin-wei, WU Chun-mi, ZHAO Yi-min Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Naringenin-5,7-di-O-¦Â-D-glucopyranoside ÏàËÆ¶È:52% Journal of Asian Natural Products Research 2003 5 25-30 GLYCOSYL FLAVONOIDS FROM THE ROOTS AND RHIZOMES OF ASARUM LONGERHIZOMATOSUM SHU-XIANG ZHANG, TADATO TANI, SEIICHI YAMAJI, CHAO-MEI MA,MIN-CHUAN WANG, SHAO-QING CAI, and YU-YING ZHAO Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . vicenin-2 C27H30O15 ÏàËÆ¶È:52% Chemistry of Natural Compounds 2012 48 672-673 Flavonoids from two Italian Genista species: Genista cilentina and Genista sulcitana C. Noccioli, L. Luciardi, S. Barsellini, C. Favro and A. Bertoli, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . vicenin II ÏàËÆ¶È:51.8% Phytochemistry 2000 53 699-704 Unusual phenolic glycosides from Cotoneaster orbicularis Amani M.D. El-Mousallamy, Sahar A.M. Hussein, Irmgard Merfort, Mahmoud A.M. Nawwar Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . vicenin II ÏàËÆ¶È:51.8% Phytochemistry 1989 28 3201-3206 Flavonoid lactates from leaves of Marrubium vulgare Mahmoud A.M. Nawwar,Amany M.D. El-Mousallamy,Heba H. Barakat,Joachim Buddrus,Michael Linscheid Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . lysidiside N C26H32O12 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(11) 1800-1805 Targeted Isolation and Structure Elucidation of Stilbene Glycosides from the Bark of Lysidice brevicalyx Wei Guided by Biological and Chemical Screening Youcai Hu, Shuanggang Ma, Jianbei Li, Shishan Yu, Jing Qu, Jing Liu, and Dan Du Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . spinosin ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 2012 43 127-136 Flavonoids from the Seeds of Zizyphus jujuba var. spinosa Lee, So-Young; Lee, Joo-Young; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-03-27 18:34:44














»Ø¸´´ËÂ¥