| ²é¿´: 213 | »Ø¸´: 1 | ||
Ò¹ò¶ù
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö
|
| 60.6,69.2,74.0,84.1,90.3,95.6,143.1,153.1,162.5, |
» ²ÂÄãϲ»¶
µç×ÓÐÅÏ¢270Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
»¯Ñ§308·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
388Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¼±Çó£ºÎ¢Æ×Êý¾ÝÇóÖú,лл
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú4¸ö΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ6È˻ظ´
¡¾SciFinderÇóÖú¡¿Ò»¸ö»¯ºÏÎï½á¹¹²éУ¨¸½cdxÎļþ£©
ÒѾÓÐ9È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò¹ò¶ù: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-17 14:30:50
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò¹ò¶ù: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-17 14:30:50
|
²éѯ½á¹û£º¹²²éµ½50¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . uridine ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2010 41 1771-1773 Chemical constituents in n-butanol extract of Abelmoschus esculentusl JIA Lu; LI Huan-fen; JING Lin-lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 4,5-diamino-1-(3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-on C9H14N4O5 ÏàËÆ¶È:66.6% Tetrahedron 2013 69 3698-3705 Fluorescent p-substituted-phenyl-imidazolo-cytidine analogues Marina Kovaliov, Meirav Segal, Bilha Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cytidine ÏàËÆ¶È:66.6% Organic Magnetic Resonance 1984 22 671-675 13C NMR studies of methylnucleosides Ching-jer Chang, Dennis J. Ashworth, Lih-Ju Chern, Jose DaSilva Gomes, Chi-Gen Lee, Pih W. Mou and Ramani Narayan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 5-formyloxymethyluridine C11H14N2O8 ÏàËÆ¶È:63.6% The Journal of Antibiotics 1990 43 584-585 A NOVEL NUCLEOSIDE ANTIBIOTIC, 5-FORMYLOXYMETHYLURIDINE KUNIO ISSHIKI, TSUTOMU SAWA, HIROSHI NAGANAWA, SEIKO HATTORI, TAKAKO IKEDA, YOSHIKO HOMMA, MASA HAMADA, TOMIO TAKEUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N3-[(Carboxyl)phosphonomethyl]uridine ÏàËÆ¶È:60% Tetrahedron 2012 68 1894-1909 Development of O-H insertion for the attachment of phosphonates to nucleosides; synthesis of a-carboxy phosphononucleosides Isabelle Hladezuk, Veronique Chastagner, Stuart G. Collins, Stephen J. Plunkett, Alan Ford, Sebastien Debarge, Anita R. Maguire* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3-methylcytidine ÏàËÆ¶È:60% Organic Magnetic Resonance 1984 22 671-675 13C NMR studies of methylnucleosides Ching-jer Chang, Dennis J. Ashworth, Lih-Ju Chern, Jose DaSilva Gomes, Chi-Gen Lee, Pih W. Mou and Ramani Narayan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4-O-methyluridine ÏàËÆ¶È:60% Organic Magnetic Resonance 1984 22 671-675 13C NMR studies of methylnucleosides Ching-jer Chang, Dennis J. Ashworth, Lih-Ju Chern, Jose DaSilva Gomes, Chi-Gen Lee, Pih W. Mou and Ramani Narayan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 5-(4-hydroxy-1-butyn-1-yl)-2'-deoxyuridine ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2010 3678-3683 Efficient Sonogashira Coupling of Unprotected Halonucleosides in Aqueous Solvents Using Water-Soluble Palladium Catalysts Joon Hyung Cho, Caitlin D. Prickett and Kevin H. Shaughnessy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (1R*,4S*)-3-bromo-4-methyl-7-oxabicyclo[2.2.1]hepta-2,5-diene-2-carboxylic acid ester ÏàËÆ¶È:55.5% Molecules 2005 10 1413-1418 Synthesis of 1-Methyl-3-oxo-7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylic Acid Methyl Ester Valquiria Aragao, Mauricio G. Constantino, Adilson Beatriz and Gil V. Jos¨¦ da Silva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . uridine ÏàËÆ¶È:55.5% Journal of Chinese Pharmaceutical Sciences 1998 7 98-99 The Chemical Constituents from the Roots of Bupleurum chinense DC. Hong Liang , Yan-Jing Bai , Yu-Ying Zhao and Ru-Yi Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . polybotrin C9H12O7 ÏàËÆ¶È:55.5% Journal of Asian Natural Products Research 2007 9 481-485 A novel compound from Hedysarum polybotrys KUN ZOU, KATSUKO KOMATSU and SHU ZHU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . polybotrin C9H12O7 ÏàËÆ¶È:55.5% Journal of Asian Natural Products Research 2007 9 699-703 A novel compound from Hedysarum polybotrys KUN ZOU, KATSUKO KOMATSU and SHU ZHU Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-10-17 14:21:28















»Ø¸´´ËÂ¥