| ²é¿´: 334 | »Ø¸´: 1 | |||
zyh201204½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖúάÆÕ~~~~~~~~~~ ÒÑÓÐ1È˲ÎÓë
|
|
CÆ×£¬ë®´úÂÈ·Â 22.5, 27.8, 31.3, 38.2, 40.6, 41.6, 44.6, 45.3, 47.4, 52.2, 53.9, 59.2, 60.8, 63.9, 66.0, 68.7, 77.3, 112.8, 140.3, 193.3, 209.2 |
» ²ÂÄãϲ»¶
323·Ö£¨¼ÆËã»úÊÓ¾õºÍ´óÄ£ÐÍÏîÄ¿£©ÄÜÖ±½ÓÉÏÊÖ
ÒѾÓÐ3È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ3È˻ظ´
311·Ö 22408 Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
320·ÖÈ˹¤ÖÇÄܵ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸Ö£´ó0705Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0703»¯Ñ§
ÒѾÓÐ10È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
306·Ö²ÄÁÏÓ뻯¹¤Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ11È˻ظ´
324Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
άÆÕÇóÖú no-3 ¼±£¡
ÒѾÓÐ4È˻ظ´
άÆÕÇóÖú--www
ÒѾÓÐ4È˻ظ´
άÆÕÇóÖú£¡Ð»Ð»~
ÒѾÓÐ3È˻ظ´
ÇóÖúscience finder Êý¾Ý¿â¼°Ïà¹Ø·´Ó¦µÄÎÄÏ×
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆÕÊý¾Ý½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ8È˻ظ´
άÆÕÇóÖú£¬¶àл
ÒѾÓÐ3È˻ظ´
Ç×°®µÄ³æÓÑÃÇ ¹òÇó½âÆ×(̼Æ× ÇâÆ× ÖÊÆ×£© ¼±
ÒѾÓÐ19È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»£¡£¡
ÒѾÓÐ3È˻ظ´
άÆÕÊý¾ÝÇóÖú£¬·Ç³£¸Ðл
ÒѾÓÐ4È˻ظ´
ÇóÖúάÆÕ лл´ó¼Ò£¡
ÒѾÓÐ3È˻ظ´
άÆÕÊý¾ÝÇóÖúX
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÃÌËáï®XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ4È˻ظ´
άÆÕÊý¾ÝÇóÖú£¡
ÒѾÓÐ4È˻ظ´
άÆÕÇóÖú£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆÕÊý¾Ý£¡¼±£¡¼±£¡¼±£¡
ÒѾÓÐ5È˻ظ´
ÇóÖúWileyÊý¾Ý¿âÈýƪÎÄÏ×
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾ÝÇóÖú£¡
ÒѾÓÐ14È˻ظ´
ÇóÖúάÆÕÊý¾Ý¿âÎÄÏ×һƪ
ÒѾÓÐ1È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
Ô¹¬ÕÛ¹ð
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 335 (´óѧÉú)
- ½ð±Ò: 3183.7
- ºì»¨: 3
- Ìû×Ó: 360
- ÔÚÏß: 57.9Сʱ
- ³æºÅ: 3524428
- ×¢²á: 2014-11-07
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh201204: ½ð±Ò+10 2014-12-18 14:09:43
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh201204: ½ð±Ò+10 2014-12-18 14:09:43
|
²éѯ½á¹û£º¹²²éµ½77¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . vilmorrianone C22H27NO4 ÏàËÆ¶È:73.9% Planta Medica 1991 57 275-277 Diterpenoid Alkaloids from Aconitum vilmorrianum Li-sheng Ding, Yao-zu Chen, and Feng-e Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . vilmorrianone ÏàËÆ¶È:69.5% Acta Chimica Sinica 1994 52 932-936 A New Skeleton Diterpenoid Alkaloid from Aconitum Vilmorinianum Kom. Ding; Li-Sheng Wu; Feng-E Chen; Yao-Zu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . neorogioldiol B C20H32O2Br2 ÏàËÆ¶È:61.9% The Journal of Organic Chemistry 2003 68 7667-7674 Novel Cytotoxic Brominated Diterpenes from the Red Alga Laurencia obtusa Dimitra Iliopoulou, Nikos Mihopoulos, Constantinos Vagias, Panagiota Papazafiri, and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7¦Á,18,19-trihydroxystemarane ÏàËÆ¶È:57.1% Phytochemistry 2002 59 57-62 Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142 Avril R.M. Chen, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . racemulodine C21H27NO4 ÏàËÆ¶È:57.1% Chinese Chemical Letters 2000 11 411-414 Diterpenoid Alkaloids from Aconitum racemulosum Franch var.pengzhouense Chong sheng PENG, Feng Peng WANG, Xi Xian JIAN,Dong Lin CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . hetidine ÏàËÆ¶È:57.1% Chinese Chemical Letters 2000 11 411-414 Diterpenoid Alkaloids from Aconitum racemulosum Franch var.pengzhouense Chong sheng PENG, Feng Peng WANG, Xi Xian JIAN,Dong Lin CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á,6¦Á-Epoxy-3¦Â-hydroxypregnan-20-one ÏàËÆ¶È:57.1% Molecules 2009 14 4655-4668 Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity Sujeong Kim and Eunsook Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2¦Á,19-dihydroxy-7¦Á,8¦Á-epoxy-9-epi-ent-pimara-15-ene C20H32O3 ÏàËÆ¶È:57.1% Phytochemistry 1998 47 211-215 The microbiological transformation of a 9-epi-ent-pimaradiene diterpene by Gibberella fujikuroi Braulio M. Fraga, Pedro Gonz¨¢lez, Melchor G. Hern¨¢ndez, Mar¨ªa C. Chamy, Juan A. Garbarino Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . hetidine C21H27NO4 ÏàËÆ¶È:57.1% Journal of Natural Products 1995 Vol 58 1555-1561 Diterpenoid Alkaloids from Delphinium albiflorum Ayhan Ulubelen, Haridutt K. Desai, Balawant S. Joshi, Vobalaboina Venkateswarlu, S. William Pelletier, Ali H. Meriçli, Filiz Meriçli, Hasan Özçelik Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 114 ÏàËÆ¶È:57.1% Natural Product Communications 2008 3 399-412 Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Ethyl Methyl (2S,3S',4S')-3-(Carboxymethyl)-4-isopropenyl-1,2-pyrrolidinedicarboxylate C15H23NO6 ÏàËÆ¶È:57.1% Journal of Medicinal Chemistry 1984 27 52-56 Palladium(II)-catalyzed olefin-coupling reactions of kainic acid: effects of substitution on the isopropenyl group on receptor binding Gregory A. Conway, Joon Sup Park, Linda Maggiora, Mathias P. Mertes, Noemi Galton, Elias K. Michaelis Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 19-acetoxy-2¦Á,7¦Á,15-trihydroxylabda-8(17),(13Z)-diene C22H36O5 ÏàËÆ¶È:54.5% Journal of Natural Products 1999 62 45-50 Novel Labdane Diterpenes from the Insecticidal Plant Hyptis spicigera1 Mabel Fragoso-Serrano, Emma Gonz¨¢lez-Chimeo, and Rogelio Pereda-Miranda Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ent-11¦Á-18-dihydroxy-6-oxo-13-epi-manoyl oxide C20H32O4 ÏàËÆ¶È:52.3% Phytochemistry 2006 67 2294-2302 Biotransformations of ent-18-acetoxy-6-ketomanoyl oxides epimers at C-13 with filamentous fungi Hanae Ghoumari, Mohamed-Hassan Benajiba, Andr¨¦s Garc¨ªa-Granados,Antonia Fern¨¢ndez, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ M. Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl ent-16¦Â,17-dihydroxy-9(11)-kauren-19-oate ÏàËÆ¶È:52.3% Phytochemistry 2003 1207-1211 Ceriopsins F and G, diterpenoids from Ceriops decandra Ammanamanchi S.R. Anjaneyulu, Vadali Lakshmana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 19-acetoxy-2¦Á,7¦Á-dihydroxylabda-14,15-dinorlabd-8(17)-en-13-one C20H32O5 ÏàËÆ¶È:52.3% Journal of Natural Products 1999 62 45-50 Novel Labdane Diterpenes from the Insecticidal Plant Hyptis spicigera1 Mabel Fragoso-Serrano, Emma Gonz¨¢lez-Chimeo, and Rogelio Pereda-Miranda Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ent-6¦Á,16¦Á,17-trihydroxyatis-13-en-11-one C20H30O4 ÏàËÆ¶È:52.3% Journal of Natural Products 1997 60 86-92 Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 21-oxogelsevirine ÏàËÆ¶È:52.3% Journal of Natural Products 1986 Vol 49 483 21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . deacetylheterophylloidine C21H27NO3 ÏàËÆ¶È:52.3% Journal of Natural Products 1995 Vol 58 1555-1561 Diterpenoid Alkaloids from Delphinium albiflorum Ayhan Ulubelen, Haridutt K. Desai, Balawant S. Joshi, Vobalaboina Venkateswarlu, S. William Pelletier, Ali H. Meriçli, Filiz Meriçli, Hasan Özçelik Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 16-Isoretuline ÏàËÆ¶È:52.3% The Journal of Organic Chemistry 1978 43 1099-1105 Carbon-13 Nulclear Magnetic Resonance Spectroscopy of Naturally Occurring Substances.56.Strychnos Alkaloids Ernest Wenkert, H.T.Andrew Cheung, and Hugo E.Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-12-18 12:01:04














»Ø¸´´ËÂ¥