| ²é¿´: 192 | »Ø¸´: 1 | |||
tjfno1ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×¾ÈÖú
|
|
13C NMR (75 MHz, MeOD) 18.10,20.76,28.86,33.65,35.63,60.97,61.39,64.28,74.36,74.76,77.84,80.56,80.83,101.41,105.04,107.13,127.05,130.98,136.99,137.30,157.34,171.28,172.37, |
» ²ÂÄãϲ»¶
286Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
0860004 Çóµ÷¼Á 309·Ö
ÒѾÓÐ3È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ20È˻ظ´
µ÷¼Á
ÒѾÓÐ11È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸0807 ÊýÒ»Ó¢Ò» 313 ÓÐûÓжþÂÖµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ14È˻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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
tjfno1: ½ð±Ò+5 2013-11-22 20:01:31
tjfno1(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-12-02 14:24:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
tjfno1: ½ð±Ò+5 2013-11-22 20:01:31
tjfno1(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-12-02 14:24:13
|
²éѯ½á¹û£º¹²²éµ½8¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . caesalpin E C24H30O7 ÏàËÆ¶È:54.1% Journal of Natural Products 2013 76 1025-1031 Caesalpins A¨CH, Bioactive Cassane-Type Diterpenes from the Seeds of Caesalpinia minax Guoxu Ma, Jingquan Yuan, Haifeng Wu, Li Cao, Xiaopo Zhang, Lijia Xu, Hua Wei, Lizhen Wu, Qingxia Zheng, Liyong Li, Lijing Zhang, Junshan Yang, and Xudong Xu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . acetylbupleurotoxin ÏàËÆ¶È:52.1% Journal of Natural Products 2009 72 2153-2157 Polyacetylenes from Bupleurum longiradiatum Hai-Qiang Huang, Xi Zhang, Yun-Heng Shen, Juan Su, Xiao-Hua Liu, Jun-Min Tian, Sheng Lin,Lei Shan, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . lobophynin A C22H34O3 ÏàËÆ¶È:52.1% Journal of Natural Products 1997 60 798-801 Bioactive Terpenoids from Octocorallia. 4. Three New Cembrane-Type Diterpenoids from the Soft Coral Lobophytum schoedei Koji Yamada, Kenjiro Ryu, Tomofumi Miyamoto, and Ryuichi Higuchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1R*,3R*3'E,5S*,6R*,7S*,8Z)-8-methyl-5-2'-acetoxy-1',5'-dimethyl-5'-hydroxyhex-3'-enyl)-2-methylenebicyclo[5.3.0]-dec-8-ene-3,6-diol C22H34O5 ÏàËÆ¶È:52.1% Planta Medica 1993 59 174-178 Four New Hydroazulenoid Diterpenes from the Tropical Marine Brown Alga Dictyota volubilis Gabriele M. Kdnig,AnthonyB. Wright , Otto Sticher,and Heinz R¨¹egger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 14-hydroxyhypocretenolide ÏàËÆ¶È:52.1% Phytochemistry 1998 49 797-800 Guaian-5,12-olides from Leontodon hispidus Christian Zidorn, Ernst P. Ellmerer-M¨¹ller, Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3,5-bis(3-methyl-2-butenyl)-4-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl] benzoic acid C29H42O13 ÏàËÆ¶È:52.1% Chinese Chemical Letters 2013 24 734-736 Five new nervogenic acid derivatives from Liparis nervosa Shuai Huang, Ming-Feng Pan, Xian-Li Zhou, Zi-Li Zhou, Cui-Juan Wang, Lian-Hai Shan, Jie Weng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 15-Hydroxygermacra-1 (10),4,11 (13)-trien-(l 2,6);(14,8)-diolide 15-O-¦Â-D-ylucopyranoside 6'-p-hydroxyphenylacetate C29H32O12 ÏàËÆ¶È:51.8% Phytochemistry 1997 45 369-373 Sesquiterpene lactones and glucosides from Urospermum picroides Basma A. A. A. Balboul, Ahmed A. Ahmed, Hideaki Otsuka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (3S)-8-[(6-O-acetyl-¦Â-D-glucopyranosyl)oxy]-3-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,4-dihydro-6-methoxy-5-methyl-1H-2-benzopyran-1-one C26H32O10 ÏàËÆ¶È:50% Helvetica Chimica Acta 2004 Vol. 87 2890 Four Novel Dihydroisocoumarin (3,4-Dihydro-1H-2-benzopyran-1-one) Glucosides from the Fungus Cephalosporium sp. AL031 Yun-Mei Bi, Xu-Bin Bi, Qian-Rong Zhao, Yuan-Teng Chen, and Jin-Lun Xie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
2Â¥2013-11-22 19:28:14














»Ø¸´´ËÂ¥