| ²é¿´: 347 | »Ø¸´: 1 | |||
ÎÂÈó×Ôº®Ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
»¯ºÏÎïCÆ×£¬ÇóÖú£¬Ð»Ð»¡£ ÒÑÓÐ1È˲ÎÓë
|
| cd3od£º18.1,26.1,29.4,62.6,62.7,71.4,71.5,75.0,75.2,78.1,78.2,78.2,78.4,103.2,103.7,115.9,117.8,119.2,123.8,133.7,133.9,152.3,154.5 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
µç×ÓÐÅÏ¢279Çóµ÷¼Á£¬ÓÐÊé¶Á¾ÍÐÐ
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
265Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
085404 298·ÖÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
348·Ö»·¾³¹¤³Ì¡¤µ÷¼Á
ÒѾÓÐ13È˻ظ´
ҩѧר˶µ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú C Æ×£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ5È˻ظ´
΢Æ× Ç󻯺ÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú½âÎöÒ»»¯ºÏÎïµÄHÆ×CÆ×£¬¸½ÉÏͼÆ×
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
ÇóÖú HÆ×ºÍCÆ×
ÒѾÓÐ15È˻ظ´
¹ØÓÚ»¯ºÏÎï̼Æ×»¯Ñ§Î»ÒƶԲ»ÉÏ£¬ÐèУÕýµÄÎÊÌâ¡£Çó¸ßÈ˽â´ð...
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
¡¾ÇóÖú¡¿¸÷λºÃ£¬ÇëÎÒ¿´Ò»¸ö¼òµ¥»¯ºÏÎïµÄHNMRÆ×ͼ¡£
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿ë®´ø»¯ºÏÎï̼Æ× Çó½âÊÍ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×È¥ñîÎÊÌâ
ÒѾÓÐ10È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÎÂÈó×Ôº®: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-11 19:18:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÎÂÈó×Ôº®: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-11 19:18:20
|
²éѯ½á¹û£º¹²²éµ½36¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,5-bis(¦Â-D-glucopyranosyloxy-2-(3',3'-dimethylallyl)benzene C23H34O12 ÏàËÆ¶È:95.6% Planta Medica 2003 69 835-841 New Pyrrolizidine Alkaloids and Glycosides from Anchusa strigosa Alessandra Braca,Ammar Bader,Tiziana Siciliano,Ivano Morelli,Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . clemomandshuricoside C C24H36O13 ÏàËÆ¶È:79.1% Helvetica Chimica Acta 2006 Vol. 89 1023 New Phenolic Glycosides from Clematis mandshurica She-Po Shi, Dan Jiang, Cai-Xia Dong, and Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . thymoquinol 5-O-¦Â-glucopyranoside C16H24O7 ÏàËÆ¶È:69.5% Phytochemistry 2001 58 1149-1152 Monoterpene glucosides from Origanum syriacum M.S. Kamel, M.H. Assaf, H.A. Hasanean, K. Ohtanib, R. Kasai, K. Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6-hydroxythymol 3,6-di-O-¦Â-D-glucopyranoside C22H34O12 ÏàËÆ¶È:69.5% Chemical & Pharmaceutical Bulletin 2001 49 840-844 Water-Soluble Constituents of Ajowan Toru ISHIKAWA, Yukiko SEGA and Junichi KITAJIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 16 C22H28O14 ÏàËÆ¶È:69.5% Bioscience, Biotechnology, and Biochemistry 2004 68 2032-2039 Glucosylation of Phenolic Compounds by Pharbitis nil Hairy Roots: I. Glucosylation of Coumarin and Flavone Derivatives Hideki KANHO, Sayaka YAOYA, Tomio ITANI, Takahisa NAKANE, Nobuo KAWAHARA, Yoichi TAKASE, Kazuo MASUDA and Masanori KUROYANAGI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . rebouoside D C26H34O14 ÏàËÆ¶È:69.2% Helvetica Chimica Acta 2011 94 1146-1152 Phenolic Glycosides from the Chinese Liverwort Reboulia hemisphaerica Li-Ning Wang, Dong-Xiao Guo, Shu-Qi Wang, Chang-Sheng Wu, Mujeeb Ur Rehman,and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . grevilloside P C24H36O16 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2014 62 364-372 Grevillosides J¨CQ, Arbutin Derivatives from the Leaves of Grevillea robusta and Their Melanogenesis Inhibitory Activity Yukiko Yamashita-Higuchi, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Takahito Nakai Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . daphnetin-7,8-di-O-disaccharide C21H26O14 ÏàËÆ¶È:65.2% |
2Â¥2015-05-11 17:22:47













»Ø¸´´ËÂ¥