| ²é¿´: 189 | »Ø¸´: 2 | ||||
yuhe0920½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×
|
| 25.2,33.6,50.8,55.8,102.6,104.9,108.3,108.6,122.7,126.0,130.7,155.8,156.3,157.3,173.2 |
» 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´

wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yuhe0920: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-07-04 11:35:53
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yuhe0920: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-07-04 11:35:53
|
°´´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£º¹²²éµ½55¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . methyl 3-(2-hydroxy-4-(7-hydroxy-6-methoxy-2-oxo-2H-chromen-3-yloxy) phenyl) propanoate C20H18O8 ÏàËÆ¶È:75% Chinese Chemical Letters 2009 20 592-594 A new coumarin from Wikstroemia indica (L.) C. A. Mey Yang Chen, Wen Wei Fu, Li Xin Sun, Qia Wang, Wei Qi, Hua Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . wikstrocoumarin ÏàËÆ¶È:75% Chemistry of Natural Compounds 2012 48 493-497 Cytotoxic constituents from Wikstroemia indica L. X. Sun, Y. Chen, L. X. Liu, Y. R. Jia and Y. C. Li, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-(2,4-dimethoxyphenyl)-2-[(4-nitrophenyl)imino]-1,3-thiazolan-4-one C17H15N3O5S ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2007 44 35-38 A novel synthesis of some 2-imino-4-thiazolidinone derivatives Firouz Matloubi Moghaddam and Leila Hojabri Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6-(2,6-dimethoxyphenyl)triazolylhexahydroxamic acid C16H22N4O4 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2008 16 4839-4853 Synthesis and structure¨Cactivity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group Po C. Chen, Vishal Patil, William Guerrant, Patience Green, Adegboyega K. Oyelere Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3R-vestitol ÏàËÆ¶È:56.2% Journal of Chinese Pharmaceutical Sciences 2006 15 178-181 Flavonoids from Millettia nitita var. hirsutissima FENG Jie; LIANG Hong; ZHAO Yu-ying; andWU Zeng-bao Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3S-vestitol ÏàËÆ¶È:56.2% Journal of Chinese Pharmaceutical Sciences 2006 15 178-181 Flavonoids from Millettia nitita var. hirsutissima FENG Jie; LIANG Hong; ZHAO Yu-ying; andWU Zeng-bao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 7,4'-dihydroxy-3'-methoxyisoflavan C16H16O4 ÏàËÆ¶È:56.2% Phytochemistry 1998 47 117-119 Isoflavonoids and a pterocarpan from Gliricidia sepium H. M. T. B. Herath, R. S. Dassanayake, A. M. A. Priyadarshani, Susila De Silva, G. P. Wannigama, Joanne Jamie Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3R)-Vestitol C16H16O4 ÏàËÆ¶È:56.2% Molecules 2011 16 9775-9782 Antibacterial Activity of the Flavonoids from Dalbergia odorifera on Ralstonia solanacearum Xiabo Zhao, Wenli Mei, Mingfu Gong, Wenjian Zuo, Hongjin Bai and Haofu Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (3S)-Vestitol ÏàËÆ¶È:56.2% Journal of Agricultural and Food Chemistry 2005 53 9010-9016 Isoflavonoids Isolated from Cuban Propolis Anna Lisa Piccinelli, Mercedes Campo Fernandez, Osmany Cuesta-Rubio, Ingrid M¨¢rquez Hern¨¢ndez, Francesco De Simone, and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (3S)-7,4'-dihydroxy-2'-methoxyisoflaVan ÏàËÆ¶È:56.2% Journal of Agricultural and Food Chemistry 2005 53 9010-9016 Isoflavonoids Isolated from Cuban Propolis Anna Lisa Piccinelli, Mercedes Campo Fernandez, Osmany Cuesta-Rubio, Ingrid M¨¢rquez Hern¨¢ndez, Francesco De Simone, and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1-{4-(2-Hydroxy-4-methoxyphenyl)-5-[4-hydroxy-3,5-bis(1-methylethyl)pyrimidin-2-yl}thiourea C24H28N4O3S ÏàËÆ¶È:55.5% Helvetica Chimica Acta 2010 93 1641-1649 One-Step Synthesis of 1-(4,5-Diphenylpyrimidin-2-yl)thiourea Wen-Yong Han, Zun-Ting Zhang, Ying-Chun Zhang, Dong Xue and Gang Li Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . stilbostemin Q C16H18O4 ÏàËÆ¶È:53.3% Phytochemistry 2008 69 457-463 Antibacterial stilbenoids from the roots of Stemona tuberosa Li-Gen Lin, Xin-Zhou Yang, Chun-Ping Tang, Chang-Qiang Ke, Ji-Bao Zhang, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . haginin D ÏàËÆ¶È:53.3% Phytochemistry 1999 52 303-310 Antioxidants from Lespedeza homoloba. (I) Toshio Miyase, Mitsuaki Sano, Haruko Nakai, Miyuki Muraoka, Miho Nakazawa, Masazumi Suzuki, Kyouji Yoshino, Yuichiro Nishihara, Junichi Tanai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-(2,4-dihydroxyphenyl)-4-(4-hydroxybenzyl)but-2-en-4-olide ÏàËÆ¶È:53.3% Phytochemistry 1997 46 921-928 Phenolic glucosides from the root of Pueraria lobata Kazuhiro Hirakura, Makoto Morita, Kaoru Nakajima, Koh Sugama, Koji Takagi, Kazuaki Niitsu, Yukinobu Ikeya, Masao Maruno, Minoru Okada Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . puerol A C17H14O5 ÏàËÆ¶È:53.3% Phytochemistry 1993 33 1207-1210 But-2-enolides from Pueraria lobata and revised structures of puerosides A, B and sophoroside A Toshihiro Nohara, Junei Kinjo, Junichi Furusawa, Yusuke Sakai, Mutsumi Inoue, Yoshiaki Shirataki, Yayoi Ishibashi (Nee Tagaya), Ichiro Yokoe, Manki Komatsu Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-30 22:10:38
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ

3Â¥2013-06-30 22:11:14














»Ø¸´´ËÂ¥