| ²é¿´: 402 | »Ø¸´: 1 | |||
Ç_Cissiľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
΢Æ×ÇóÖú£º ë®´úÊÔ¼Á£ºDMSO 16.7 ,17.4 ,18.0 ,19.5 ,29.1 ,38.5 ,41.6 ,44.6 ,45.6 ,47.0 ,82.5 ,114.9 ,116.2 ,125.4 ,130.9 ,145.1 ,160.4 ,167.1 лл£¡ [ Last edited by ׿Խ_ÏÈ·æ on 2015-6-7 at 11:07 ] |
» ²ÂÄãϲ»¶
µ÷¼Á
ÒѾÓÐ17È˻ظ´
347²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
Çó¿¼ÑвÄÁϵ÷¼Á
ÒѾÓÐ3È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©×ö¹ý·Ö×ÓʵÑé
ÒѾÓÐ6È˻ظ´
¼ÆËã»ú408£üÔÚУ¶à´Î¹ú¼Ò¼¶¾ºÈü»ñ½±£üÉêÇëµ÷¼Á
ÒѾÓÐ4È˻ظ´
388Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
288Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ29È˻ظ´
266µ÷¼Á
ÒѾÓÐ6È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
» ±¾Ö÷ÌâÏà¹ØÉ̼ÒÍÆ¼ö: (ÎÒÒ²ÒªÔÚÕâÀïÍÆ¹ã)

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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ç_Cissi: ½ð±Ò+8 2015-06-07 11:15:17
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ç_Cissi: ½ð±Ò+8 2015-06-07 11:15:17
|
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%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½58¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Coprophilin C19H28O3 ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry Letters 1998 8 3439-3442 Coprophilin: An anticoccidial agent produced by a dung inhabiting fungus John G. Ondeyka, Robert A. Giacobbe, Gerald F. Bills, Cristina Cuadrillero, Dennis Schmatz, Michael A. Goetz, Deborah L. Zink, Sheo B. Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . hyrtiophenol C23H32O3 ÏàËÆ¶È:56.5% Journal of Natural Products 2000 63 452-456 New Sesquiterpene/Quinones from Two Sponges of the Genus Hyrtios M. Salmoun, C. Devijver, D. Daloze, J. C. Braekman,R. Gomez, M. de Kluijver, and R. W. M. Van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-bornyl p-coumarate ÏàËÆ¶È:55.5% Phytochemistry 1997 44 1265-1270 A comparative study on three chemo-types of the liverwort Conocephalum conicum using volatile constituents Masao Toyota, Tetsuya Saito, Junko Matsunami, Yoshinori Asakawa* Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6,6,8-Èý¼×»ù-5,7-ÑǼ׻ùÇÅ-4-(4'-·ú±½»ù)-5,6,7,8-ËÄÇâàßòßø-2-°· C18H21N3F ÏàËÆ¶È:55.5% Chinese Journal of Organic Chemistry 2014 34 2130¨C2134 Synthesis and Biological Activities of Novel 4-Aryl-5,6,7,8-tetrahydroquinazolin-2-amine Derivatives Bao, Mingkai Xiong, Sisi Cao, Mingzhen Xu, Xu Wang, Shifa*, Zhang, Zhijie Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Alkaline hydrolysis of rufisoside B ÏàËÆ¶È:55% Phytochemistry 1993 32 151-153 Diterpene glycosides from Senecio rufus Dong-Liang Cheng, Xiao-Ping Cao, Jie-Kai Cheng, E. Roeder Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 16-bromomethylestra-1,3,5(10)-triene-3,17-diol 7e C19H25O2Br ÏàËÆ¶È:52.6% Steroids 2006 71 141-153 Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols ¨¢gota Sz¨¢jli, J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Ren¨¢ta Minorics, ¨¢rp¨¢d M¨¢rki, George Falkay, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . hymenophylloide C20H30O4 ÏàËÆ¶È:52.6% Phytochemistry 1989 28 2741-2744 Diterpenes from Fleischmannia hymenophylla and Brickellia laciniata J. Jakupovic,F. Tsichritzis,G. Tamayo-Castillo,V. Castro,F. Bohlmann,E. Boldt Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-06-07 10:52:05














»Ø¸´´ËÂ¥