| ²é¿´: 699 | »Ø¸´: 1 | ||
[ÇóÖú]
hua
|
| 55.40,55.44,110.54,112.64,114.59,115.18,115.24,122.11,122.86,123.89,126.56,144.88,147.19,147.91,149.10,151.13 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³ÌרҵÈÕÓïÉúÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ12È˻ظ´
»úеר˶273ÇëÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
080100Á¦Ñ§316Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ39È˻ظ´
wangwang1989
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 525 (²©Ê¿)
- ½ð±Ò: 11769.2
- É¢½ð: 1451
- ºì»¨: 21
- ɳ·¢: 18
- Ìû×Ó: 4912
- ÔÚÏß: 315.2Сʱ
- ³æºÅ: 1467486
- ×¢²á: 2011-10-30
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+1, 3u 2013-06-29 22:32:11
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+1, 3u 2013-06-29 22:32:11
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Tribulusimide D C18H17NO6 ÏàËÆ¶È:88.8% Archives of Pharmacal Research 2010 33 67-70 Tribuli fructus constituents protect against tacrine-induced cytotoxicity in HepG2 cells Erisa Byun, Gil-Saeng Jeong, Ren-Bo An, Tae Sun Min and Youn-Chul Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (E)-3-(4-hydroxy-2-methoxy-phenyl)-propenoic acid 4-hydroxy-3-methoxyphenyl ester C17H16O6 ÏàËÆ¶È:76.4% Chinese Journal of Natural Medicines 2009 7 351-353 A New Phenylpropionate Derivative from the Rhizomes of Hedysarum polybotrys CHENG Fan; ZOU Kun; ZHU Shu; KATSUKO Komatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-hydroxy-3-methoxyphenyl ferulate C17H16O6 ÏàËÆ¶È:70.5% Planta Medica 2005 71 680-682 Cytotoxicities of Xanthones and Cinnamate Esters from Hypericum hookerianum Rujida Wilairat, Jiradej Manosroi , Aranya Manosroi,Anake Kijjoa,Maria São Jos¨¦ Nascimento ,Madalena Pinto ,Artur M. S. Silva ,Graham Eaton,Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7,8-dihydroxy-3',4',-dimethoxyisoflavone C17H14O6 ÏàËÆ¶È:70.5% Chemical & Pharmaceutical Bulletin 2009 57 346-360 Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities Hideyuki Goto, Yoshiyasu Terao and Shuji Akai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4',8-dihydroxy-3',7-dimethoxyisoflavone C17H14O6 ÏàËÆ¶È:70.5% Chemical & Pharmaceutical Bulletin 2009 57 346-360 Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities Hideyuki Goto, Yoshiyasu Terao and Shuji Akai Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Compound 19a ÏàËÆ¶È:70.5% Magnetic Resonance in Chemistry 2008 46 299-305 1H and 13C NMR data of benzylsulfonic acids¡ªmodel compounds for lignosulfonate (pages 299¨C305) Bjart F. Lutnaes, Bernt O. Myrvold, Rolf A. Lauten and Molla M. Endeshaw Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3,4-dihydroxy-3',4'-dimethoxydeoxybenzoin C16H16O5 ÏàËÆ¶È:70.5% Bioorganic & Medicinal Chemistry 2009 17 4360-4366 Potential antioxidants and tyrosinase inhibitors from synthetic polyphenolic deoxybenzoins Lean-Teik Ng, Horng-Huey Ko, Tzy-Ming Lu Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-29 21:49:27














»Ø¸´´ËÂ¥