| ²é¿´: 342 | »Ø¸´: 1 | |||
xiabohouľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¡·Ç³£¸Ðл£¡£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
| 19.32,21.91,28.83,29.21,30.00,31.85,32.32,32.65,33.23,34.03,35.51,35.62,37.46,37.81,40.42,40.50,40.63,44.33,45.04,45.74,46.45,46.55,46.73,48.28,59.66,64.32,66.45,67.82,70.90,70.99,73.00,81.41,92.97,121.20,128.41,145.78,151.59,172.84 |
» ²ÂÄãϲ»¶
Çà»ùÈçºÎÆÆ¾Ö
ÒѾÓÐ7È˻ظ´
ÓжàÉÙÈËÊǽñÌì²éϵͳ֪µÀ½á¹ûµÄ£¿
ÒѾÓÐ17È˻ظ´
»ù½ð²»ÖУ¬¹²Ãã
ÒѾÓÐ10È˻ظ´
¹ú×ÔÈ»ÃæÉϸ´ÅÌ~»¶ÓÌÖÂÛ
ÒѾÓÐ11È˻ظ´
Ϊʲô×ÊÖúÊý¸÷´ó¸ßУ¶¼´´Ð¸ߣ¬×Ô¼ºÉêÇëÔõô¾ÍÕâôÄÑ
ÒѾÓÐ7È˻ظ´
»ù½ðδÖУ¬ÕâÖÖ´ð¸´ÊÇÄ£°åÂð£¿
ÒѾÓÐ6È˻ظ´
¿´°åÉÏÕâô¶àÖеģ¬ÓеãÏñ50ÈËȺÀï49¸öÈ˶¼ÊÇÆ×ÓµÄÄÇÖָоõ¡¡
ÒѾÓÐ6È˻ظ´
µ¼Ê¦Í²ۣºÎÒÔõô̯ÉÏÁËÕâô¸ö¼«Æ·Ñо¿Éú£¡
ÒѾÓÐ6È˻ظ´
Ôõô¿´Çà»ùÖÐÁËûÓа¡
ÒѾÓÐ5È˻ظ´
ÃÎÏë
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»´óÉñ£¡
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ5È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ3È˻ظ´
phytochemistry Ͷ¸å
ÒѾÓÐ24È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
MESTRENOVA 7 ½â̼Æ×£¬ÈçºÎÈÃÊä³öµÄÊý¾Ý±£ÁôһλСÊý£¨Ä¬ÈÏÊÇÁ½Î»£©£¿
ÒѾÓÐ12È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»¾äרҵ·Òë luminescence units normalized for ¦Â-galactosidase expression,
ÒѾÓÐ3È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12673.8
- ºì»¨: 16
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½333¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . wattoside B C34H57O12 ÏàËÆ¶È:57.8% Acta Botanica Yunnanica 2001 23(3) 373-380 New Steroidal Glycosides from Tupistra wattii YANG Fan, SHEN Ping,WANG Yi-Fei,ZHANG Ren-Yan, YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-amyrin-3-palmitate C46H80O2 ÏàËÆ¶È:57.8% Chinese Journal of Natural Medicines 2007 5 259-262 Non-alkaline Constituents From the Leaf of Alstonia scholaris DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Olean-12-en-3¦Â,16¦Â-diol-3-O-palmitate ÏàËÆ¶È:57.8% Pharmazie 2006 61 70-73 Triterpenoids from Pyrethrum tatsienense Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-L-alanyl]-glycine C35H56N2O6 ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry 2009 17 1139-1145 Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides Andres Parra, Francisco Rivas, Pilar E. Lopez, Andres Garcia-Granados, Antonio Martinez, Fernando Albericio, Nieves Marquez, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . caulophyllogenin-3-O-¦Á-L-arabinopyranoside C35H56O9 ÏàËÆ¶È:57.8% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . pukeensine C44H64N2O3 ÏàËÆ¶È:57.5% Acta Pharmaceutica Sinica 1992 27 394-396 A NEW SKELETON BISDITERPENOID ALKALOID FROM ACONITUM PUKEENSE LS Ding; FE Wu; YZ Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-¦Â-D-galactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl quillaic acid ÏàËÆ¶È:57.1% Phytochemistry 1995 40 509-514 Acylated triterpene saponins from Silene jenisseensis Marie-Aleth Lacaille-Dubois, Bernard Hanquet, Zhen-Hua Cui, Zhi-Cen Lou, Hildebert Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Lilioglycoside C C39H60O13 ÏàËÆ¶È:56.4% Chemistry of Natural Compounds 1997 33 658-662 sTRuCTURES OF SOME LILIOGLYCOSIDES FROM THE BULBS OF Lilium regale P. K. Kintya, A. S. Gur'eva, N. E. Mashchenko,and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N-[3-(6-aminohexyl)aminocarbonyl]propyl-2-cyano-3,12-dioxooleana-1,9(11)-dien-28-amide trifluoroacetate C41H62N4O4 ÏàËÆ¶È:56.4% Journal of Medicinal Chemistry 2004 47 4923-4932 Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N''-[N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-6-aminohexanoyl]-L-alanyl]-glycine C41H67N3O7 ÏàËÆ¶È:56.0% Bioorganic & Medicinal Chemistry 2009 17 1139-1145 Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides Andres Parra, Francisco Rivas, Pilar E. Lopez, Andres Garcia-Granados, Antonio Martinez, Fernando Albericio, Nieves Marquez, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Á,3¦Â,21¦Â-trihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C36H58O10 ÏàËÆ¶È:55.2% Planta Medica 2009 75 522-527 Antimicrobial Pentacyclic Triterpenoids from Terminalia superba Turibio Kuiate Tabopda, Joseph Ngoupayo, Sheraz A. Khan Tanoli, Anne-Claire Mitaine-Offer,Bonaventure Tchaleu Ngadjui, Muhammad Shaiq Ali, Bang Luu, Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . brevicuspisaponin 2 C35H56O10 ÏàËÆ¶È:55.2% Phytochemistry 2000 53 901-904 Triterpenoid glycosides and a triterpene from Ilex brevicuspis Alexandre T. Cardoso Taketa, Tatjana Schmittmann-Schlager, Dominique Guillaum, Grace Gosmann, Eloir Paulo Schenkel Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (22S,25R)-Furost-5-ene-3¦Â,22,26-triol 22-O-(¦Á-D-glucopyranoside) C33H54O9 ÏàËÆ¶È:55.2% Steroids 2011 76 18-27 The synthesis of cholestane and furostan saponin analogues and the determination of sapogenin¡¯s absolute configuration at C-22 Haixing Wang, Yanshen Guo, Yuyao Guan, Liang Zhou, Pingsheng Lei Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (22R,25R)-Furost-5-ene-3¦Â,22,26-triol 22-O-(¦Á-D-glucopyranoside) C33H54O9 ÏàËÆ¶È:55.2% Steroids 2011 76 18-27 The synthesis of cholestane and furostan saponin analogues and the determination of sapogenin¡¯s absolute configuration at C-22 Haixing Wang, Yanshen Guo, Yuyao Guan, Liang Zhou, Pingsheng Lei Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . olean-12-en-3¦Â,15¦Á-yl diacetate ÏàËÆ¶È:55.2% Phytochemistry 1988 27 3653-3657 Alkaloids from Alstonia macrophylla Atta-ur-rahman,Gulzar Ahmed,M.Iqbal Choudhary,Habib-ur-rehman,K.T. De Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 23-hydroxyimberbic acid-23-O-¦Á-L-4-acetyl-rhamnopyranoside ÏàËÆ¶È:55.2% Chinese Traditional and Herbal Drugs 2008 39 512-514 éÐη糵×ÓÒ¶ÖÐÝÆÀ໯ºÏÎïµÄÑо¿ ÎâÏþÅô;³Â¹âÓ¢;½¯²ÅÎä;Öì¹úÔª;·½ºêÑ« Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ÉßÝÔËØ A ÏàËÆ¶È:55.2% Chinese Traditional and Herbal Drugs 2005 36 830-831 ˼éÉßÝԵĻ¯Ñ§³É·ÖÑо¿(¢ñ) ´÷ÖÒ,Íõ¸ÖÁ¦,Íõ·å,ÂíË«³É,ÁÖÈ𳬠Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Pinnatoxin B ÏàËÆ¶È:55.2% Tetrahedron Letters 2001 42 3491-3494 Pinnatoxins B and C, the most toxic components in the pinnatoxin series from the Okinawan bivalve Pinna muricata Noboru Takada, Naoyoshi Umemura, Kiyotake Suenaga, Tong Chou, Akito Nagatsu, Takeharu Haino, Kaoru Yamada, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Pinnatoxin C ÏàËÆ¶È:55.2% Tetrahedron Letters 2001 42 3491-3494 Pinnatoxins B and C, the most toxic components in the pinnatoxin series from the Okinawan bivalve Pinna muricata Noboru Takada, Naoyoshi Umemura, Kiyotake Suenaga, Tong Chou, Akito Nagatsu, Takeharu Haino, Kaoru Yamada, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-amyrin 3-palmitate C46H50O2 ÏàËÆ¶È:55.2% Natural Product Research and Development 1998 10(3) 20-23 TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA Liu Xikui; Chiu Minghua; Li Zhongrong Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 22-methoxy-5¦Â-furostane-1¦Â,3¦Â,4¦Â,5¦Â,26-pentaol 26-O-¦Â-D-glucopyranoside ÏàËÆ¶È:55.2% Natural Product Research and Development 1995 7(1) 19-23 STEROIDAL GLYCOSTDES FROM ASPIDISTRA SICHUANENSTS K. Y. LANG ET Z. Y. ZHU Chen Mengjing Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4''-O-[3-(1,2,3,4-tetrahydro-3-quinolinyl)propanoyl]-8a-aza-8a-homoerythromycin A C49H81N3O14 ÏàËÆ¶È:55.2% The Journal of Antibiotics 2009 62 133-144 Synthesis and biological properties of 4"-O-acyl derivatives of 8a-Aza-8a-homoerythromycin Vlado Stimac, Sulejman Alihodzic, Gorjana Lazarevski, Stjepan Mutak, Zorica Marusic Istuk, Andrea Fajdetic, Ivana Palej, Hana Cipcic Paljetak, Jasna Padovan, Branka Tavcar and Vesna Erakovic Haber Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (4R,4¦ÁR,4¦ÂR,6¦ÁR,7R,8R,10¦ÁR,10¦ÂR,12¦ÁR)-hexadecahydro-¦Á8,¦Á8,3,3,7,10¦Á,10¦Â-heptamethyl-13-oxo-7-{2-oxo-2-[(2-phenylethyl)amino]ethyl}-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid C38H55NO5 ÏàËÆ¶È:55.2% Helvetica Chimica Acta 2013 96 1757-1781 Synthesis of Nitrogen-Containing Derivatives of (18,19¦Â)-19-Hydroxy-2,3-secooleanane-2,3,28-trioic Acid 28,19-Lactone Andrey V. Shernyukov, Ilya Ya. Mainagashev, Dina V. Korchagina, Alexander M. Genaev, Nina I. Komarova, Nariman F. Salakhutdinov and Genrikh A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (4'R,4''R,2'''S,¦ÁR)-1-[2'-Oxo-4'-pentyl-N(5')-methyl-1',5'-diazocan-N(1')-yl]-4-{2''-oxo-4''-[2'''-(benzyloxy)heptyl]-N(5'')-(¦Á-methylbenzyl)-1'',5''-diazocan-N(1')-yl}butane C44H70N4O3 ÏàËÆ¶È:55.2% The Journal of Organic Chemistry 2012 77 9724-9737 Absolute Configuration Assignment by Asymmetric Syntheses of the Homalium Alkaloids (− -(R,R,R)-Hoprominol and (− -(4¡äS,4¡åR,2‴R)-HopromalinolStephen G. Davies, James A. Lee, Paul M. Roberts, Jeffrey P. Stonehouse, and James E. Thomson Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 10c C38H64O7 ÏàËÆ¶È:55.2% Steroids 2013 78 651-661 Synthesis of various secosteroidal macrocycles by ring-closing metathesis Malika Ibrahim-Ouali, Eug¨¦nie Romero Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 3¦Â-Acetoxy-28-oxo-28-[3-acetyl-(3-aminopropyl)-amino]lup-20(29)-ene C37H60N2O2 ÏàËÆ¶È:55.2% Russian Journal of Bioorganic Chemistry 2013 39 329-337 Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-08-08 17:10:15









»Ø¸´´ËÂ¥
-(R,R,R)-Hoprominol and (−
ͶƱ: