| ²é¿´: 316 | »Ø¸´: 1 | |||
ÓÍÌï±ø¶¡Í³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú£¡ ÒÑÓÐ1È˲ÎÓë
|
| 13CNMR(CDCL3) 19.44,21.39,25.51,26.83,69.26,69.31,76.30,108.08,109.19,110.62,115.68,122.23,125.50,131.19,137.08,140.67,150.56,151.29,156.49,159.06, |
» ²ÂÄãϲ»¶
288Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸ÏôóÉúÎïѧ332Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏ»¯¹¤×Ü·Ö334Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ20È˻ظ´
Ò»Ö¾Ô¸Öпƴó070300»¯Ñ§£¬314·ÖÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
¸÷λÐÂÄêºÃ ÇóÖú΢Æ× Éͽð80 ÒѾ°´ÕÕ΢Æ×¸ñʽÕûÀíºÃ ллÁË
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48419.9
- ºì»¨: 52
- Ìû×Ó: 6747
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÓÍÌï±ø¶¡: ½ð±Ò+8, ¡ïÓаïÖú 2015-06-05 16:03:27
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÓÍÌï±ø¶¡: ½ð±Ò+8, ¡ïÓаïÖú 2015-06-05 16:03:27
|
1 . 4,5,7,4'-tetraacetateisoflavanone ÏàËÆ¶È:60% Journal of Natural Products 1995 Vol 58 1901-1905 Metabolites of Daidzein and Genistein and Their Biological Activities Yu-Chen Chang, Muraleedharan G. Nair, John L. Nitiss Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . taiwaniaquinol E C20H28O4 ÏàËÆ¶È:55% Planta Medica 2005 71 72-76 Four New 6-Nor-5(6¡ú7)abeo-abietane Type Diterpenes and Antitumoral Cytotoxic DiterpeneConstituents from the Bark of Taiwaniacryptomerioides Chi-I Chang,Jang-Yang Chang,Ching-Chuan Kuo,Wen-Yu Pan,Yueh-Hsiung Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-(5-allyl-2-hydroxy-3-methoxyphenyl)-1-(4-hydroxy-3-methoxyphenoxy)-prop-1-ene C20H22O5 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2009 57 245-251 Leishmanicidal Active Constituents from Nepalese Medicinal Plant Tulsi (Ocimum sanctum L.) Akiko Suzuki, Osamu Shirota, Kanami Mori, Setsuko Sekita, Hiroyuki Fuchino, Akihito Takano and Masanori Kuroyanagi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . lyratin C C20H23O6 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2010 58 840-842 New Anti-inflammatory 4-Hydroxyisoflavans from Solanum lyratum De-Wu Zhang, Gui-Hai Li, Qun-Ying Yu and Sheng-Jun Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . penicillazine C20H20N2O9 ÏàËÆ¶È:55% Tetrahedron 2000 56 9607-9609 Penicillazine, a Unique Quinolone Derivative with 4H-5,6-Dihydro-1,2-oxazine Ring System from the Marine Fungus Penicillium sp. (Strain #386) from the South China Sea Yongcheng Lin, Zhiyu Shao, Guangce Jiang, Shining Zhou, Jiwen Cai, L.L.P Vrijmoed, E.B Gareth Jones Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . awajanoran C19H22O4 ÏàËÆ¶È:55% The Journal of Antibiotics 2006 59 428-431 New Dihydrobenzofuran Derivative, Awajanoran, from Marine-derived Acremonium sp. AWA16-1 FREE Jae-Hyuk Jang, Kaneo Kanoh, Kyoko Adachi and Yoshikazu Shizuri Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . erythrinin G C20H18O6 ÏàËÆ¶È:55% Natural Products and Bioprospecting 2013 3 238-242 New isoflavonoids from Erythrina arborescens and structure revision of anagyroidisoflavone A Fei Wang, Xu-Long Li, Guo-Zhu Wei, Fu-Cai Ren¡ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-04 21:19:44













»Ø¸´´ËÂ¥
5