| ²é¿´: 267 | »Ø¸´: 2 | |||
Ñî´óËÉÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
|
|
̼Æ×Êý¾ÝÈçÏ£º 10.3,17.6,18.3,22.0,28.9,30.1,37.8,37.9,45.7,47.9,55.3,58.7,67.7,127.4,142.5,157.5 ÐÁ¿à¸÷λÁË£¬Ð»Ð»¡£ |
» ²ÂÄãϲ»¶
070300»¯Ñ§279Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏ¿¼Ñе÷¼Á
ÒѾÓÐ19È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ41È˻ظ´
Çóµ÷¼Á£¬262»úеר˶
ÒѾÓÐ7È˻ظ´
266Çóµ÷¼Á£¬Ò»Ö¾Ô¸¹þ¹¤³Ìµç×ÓÐÅÏ¢£¬±¾¿Æ»ñ¶àÏî¹ú½±ºÍÊ¡½±
ÒѾÓÐ6È˻ظ´
0860004 Çóµ÷¼Á 309·Ö
ÒѾÓÐ8È˻ظ´
270Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
347Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
280Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
ҩѧ305Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´

¶þÂȼ×Íé
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 105 (¸ßÖÐÉú)
- ½ð±Ò: 2190.7
- É¢½ð: 1870
- ºì»¨: 15
- Ìû×Ó: 538
- ÔÚÏß: 120.8Сʱ
- ³æºÅ: 1337209
- ×¢²á: 2011-07-04
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñî´óËÉ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-07-23 17:40:41
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñî´óËÉ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-07-23 17:40:41
|
1 . langduin A C20H28O5 ÏàËÆ¶È:70% Phytochemistry 1997 44 663-666 Diterpenoids from Euphorbia fischeriana Qing-Gao Ma, Wen-Zi Liu, Xiao-Yun Wu, Tian-Xi Zhou, Guo-Wei Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . huperzine K C16H28N2O ÏàËÆ¶È:68.7% Planta Medica 2000 66 664-667 Three Lycopodium Alkaloid N-Oxides from Huperzia serrata Wenyun Gao,Yiming Li,Shanhao Jiang,Dayuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-Methoxyestra-1,3,5(10)-triene-16¦Á,17¦Á-diol C19H28O3 ÏàËÆ¶È:58.8% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . elongatol C C15H24O3 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2007 55(5) 762-765 Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata Shang-Kwei WANGa and Chang-Yih DUH Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (4aR,5S,6R,8aR)-Decahydro-5-(2-hydroxyethyl)-1,5,6,8¦Á-tetramethylnaphthalen-2-ol C16H30O2 ÏàËÆ¶È:56.2% Chemistry & Biodiversity 2009 6 447-458 Structure¨C Activity Relationship Studies on the Mosquito Toxicity and Biting Deterrency of Callicarpenal Derivatives Charles L. Cantrell, Jerome A. Klun, Julia Pridgeon, James Becnel, Solomon Green III, and Frank R. Fronczek Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . herbolide D ÏàËÆ¶È:56.2% Phytochemistry 1984 23 2954-2956 Sesquiterpene lactones from a further population of Artemisia herba alba R. Segal, L. Eden, A. Danin, M. Kaiser, H. Duddeck Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . herbolide E ÏàËÆ¶È:56.2% Phytochemistry 1985 24 1381-1382 Sesquiterpene lactones from Artemisia herba alba, R. Segal, L. Eden, A. Danin, M. Kaiser, H. Duddeck Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Undec-10-ynoic acid (1-phenylethyl)amide ÏàËÆ¶È:56.2% Archiv der Pharmazie 2007 340 154-158 Synthesis and Biological Evaluation of New Niphathesine Analogues J¨¹rgen Krauss, Christine Wetzel, Julia Thiel, Christine Neudert and Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Cyanthiwigin Y C20H30O2 ÏàËÆ¶È:55% Tetrahedron 2002 58 7809-7819 The new bioactive diterpenes cyanthiwigins E¨CAA from the Jamaican sponge Myrmekioderma styx Jiangnan Peng, Kelly Walsh, Valarie Weedman, Jennifer D Bergthold, John Lynch, Kuo L Lieu, Irwin A Braude, Michelle Kelly, Mark T Hamann Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . huperzine J C17H30N2O ÏàËÆ¶È:52.9% Planta Medica 2000 66 664-667 Three Lycopodium Alkaloid N-Oxides from Huperzia serrata Wenyun Gao,Yiming Li,Shanhao Jiang,Dayuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1¦Á,2¦Á-Epoxy-1,4--androstadien-3¦Â,17¦Â-diol ÏàËÆ¶È:52.6% Molecules 2005 10 572-582 Epoxidation and Reduction of DHEA, 1, 4, 6-Androstatrien-3-one and 4, 6-Androstadien-3¦Â, 17¦Â-diol Eunsook Ma and Eunjeong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 6¦Á,12-diacetoxy-4¦Á-hydroxy-5¦Á,11¦Â-H-eudesman-1-one C19H30O6 ÏàËÆ¶È:52.6% Tetrahedron 2000 56 6517-6526 Chemical Semisynthesis and Biotransformation with Rhizopus nigricans of Several Sesquiterpenes: Obtention of New 1¦Á- and 2¦Á-Hydroxyselinane Derivatives Andr¨¦s Garc??a-Granados, Enrique Melguizo, Andr¨¦s Parra, Felipe L P¨¦rez, Yolanda Sime¨®, Beatriz Viseras, Jos¨¦ Mar??a Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ustusol A C15H24O4 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 1761-1767 Sesquiterpenoids and Benzofuranoids from the Marine-Derived Fungus Aspergillus ustus 094102 Zhenyu Lu, Yi Wang, Chengdu Miao, Peipei Liu, Kui Hong, and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . sinodielide A C15H20O2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2003 51(1) 68-70 Four Guaianolides from Sinodielsia yunnanensis Nian-He WANG,Masahiko TANIGUCHI, Daisuke TSUJI, Mitsunobu DOI,Hirohumi OHISHI, Kenji YOZA,c and Kimiye BABA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (1S,4S,5S,6R,7S,10S)-dihydroxymaaliane C15H26O2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2000 48(11) 77-80 Three New Sesquiterpenoid Glucosides of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA,and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-¦Á-Chamipinene, (1S,6S,7S)-2,2,6,8-tetramethyltricyclo[5.3.1.01,6]undec-8-ene C15H24 ÏàËÆ¶È:50% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-eudesma-3,11-dien-8-one C15H22O ÏàËÆ¶È:50% Phytochemistry 2003 64 637-644 Volatile constituents in the liverwort Tritomaria polita Adewale Martins Adio, Claudia Paul, Wilfried A. K?nig, Hermann Muhle Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . jewenol A ÏàËÆ¶È:50% Phytochemistry 2002 60 339-343 Clerodane and labdane diterpene glycosides from a Malagasy endemic plant, Cussonia racemosa R.R. Harinantenaina Liva, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2012-07-23 13:23:43
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

3Â¥2012-07-23 17:40:53













»Ø¸´´ËÂ¥