| ²é¿´: 228 | »Ø¸´: 1 | ||||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ
|
|
ÈܼÁ£º¼×´¼ ÏàËÆ¶È£º90%ÒÔÉÏ ºË´ÅÊý¾Ý£º 12.6,15.7,24.0,27.8,36.4,38.6,43.0,43.6,55.7,61.4,66.6,67.0,73.7,126.3,138.5 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ12È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ15È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ10È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ37È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì322
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ25È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¶àл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
journal of molecular structureͶ¸åÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´

wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-17 23:26:19
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-17 23:26:19
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½112¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3S,4S,9R,10S-11,12,14-tri-hydroxydrimene ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 7 874-880 Studies on constituents of cultures of fungus Phellinu signiarius WU Xiu li,LIN Sheng, ZHU Chenggen, ZHAO Feng, YU Yang, YUE Zhenggang, LIU Bo,YANG Yong chun, DAI Jungui, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 11,12,14-trihydroxydrimene C15H26O3 ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 1889 67 1371-1380 Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin William A. Ayer, Peter Craw Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3,11,12-trihydroxydrimene ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 1889 67 1371-1380 Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin William A. Ayer, Peter Craw Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7¦Â-hydroxy-10-deoxoartemisinin C15H24O5 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 1595-1597 Hydroxylation of 10-Deoxoartemisinin by Cunninghamella elegans Igor A. Parshikov, Kannoth M. Muraleedharan, Bruhaspathy Miriyala, Mitchell A.Avery,and John S. Williamson Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-11,12-dihydroxydrimene C15H26O2 ÏàËÆ¶È:60% The Journal of Antibiotics 1994 47 1017-1024 THE MNIOPETALS, NEW INHIBITORS OF REVERSE TRANSCRIPTASES FROM A Mniopetalum SPECIES (BASIDIOMYCETES) II. STRUCTURE ELUCIDATION ROBERT VELTEN, DÖRTE KLOSTERMEYER, BERT STEFFAN, WOLFGANG STEGLICH, ANDREA KUSCHEL, TIMM ANKE Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7¦Â-hydroxy-10-deoxoartemisinin ÏàËÆ¶È:60% Biotechnology Letters 2004 26 607-610 Hydroxylation of 10-deoxoartemisinin to 15-hydroxy-10-deoxoartemisinin by Aspergillus niger Igor A. Parshikov, Bruhaspathy Miriyala, Mitchell A. Avery, John S. Williamson Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 1 C15H26O3 ÏàËÆ¶È:60% Natural Product Communications 2008 3 1747-1750 New Drimane Sesquiterpenoids from Tidestromia oblongifolia Sandeep Chaudhary , Vladimir Thomas, Louis Todaro, Onica LeGendre, Stevan Pecic and Wayne W. Harding Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Xerophilusin XIV C20H34O4 ÏàËÆ¶È:60% Archives of Pharmacal Research 2011 34 875-879 ent-Abietane Diterpenoids from Isodon xerophilus Li Mei Li, Jian Xin Pu, Wei Lie Xiao, and Han Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . oidiolactone F C16H22O5 ÏàËÆ¶È:56.2% Journal of Natural Products 1999 62 1218-1221 Biologically Active Secondary Metabolites from Fungi. 12.1 Oidiolactones A-F, Labdane Diterpene Derivatives Isolated from Oidiodendron truncata Markus John, Karsten Krohn, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger, and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 15 ÏàËÆ¶È:56.2% Phytochemistry 1994 35 713-719 Compounds with the labdane skeleton from Halimium viscosum Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-desacyl-4¦Â-hydroxy-15-dihydrocarmanin C16H26O7 ÏàËÆ¶È:56.2% Phytochemistry 1992 31 3630-3632 Sesquiterpenes, flavonoids and lignans from Onopordon acaulon Luz Cardona, Rafael A. Alemañ, Begoña Garcia, Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-09-16 13:35:07














»Ø¸´´ËÂ¥