| ²é¿´: 699 | »Ø¸´: 1 | ||
¿ÓµùÒ©»¯Ìú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú¼±¼±¼±£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
| CÆ×Êý¾Ý£º23.09, 23.12,23.13,24.87,25.23,25.33,26.30,34.28,48.26, 54.10,57.21,94.87,105.57,108.90,114.57,127.38,128.98,129.28,145.81,156.02,161.80,164.51,166.74,198.71,208.02,212.79 |
» ²ÂÄãϲ»¶
»ù½ðϵͳʲôÄÚÈÝҲûÓÐ
ÒѾÓÐ6È˻ظ´
ÓжàÉÙÈËÊǽñÌì²éϵͳ֪µÀ½á¹ûµÄ£¿
ÒѾÓÐ17È˻ظ´
¹ú×ÔÈ»ÃæÉϸ´ÅÌ~»¶ÓÌÖÂÛ
ÒѾÓÐ12È˻ظ´
Ϊʲô×ÊÖúÊý¸÷´ó¸ßУ¶¼´´Ð¸ߣ¬×Ô¼ºÉêÇëÔõô¾ÍÕâôÄÑ
ÒѾÓÐ9È˻ظ´
ÊÛSCIÒ»ÇøÎÄÕ£¬ÎÒ:8O5.5.1.O5.4,¿ÆÄ¿È«,¿ÉÙ¤¼±
ÒѾÓÐ3È˻ظ´
ÄÄλ¸ßÈËÖÐÁË£¬°Ñ²éѯµ½µÄ½ØÍ¼Ìù³öÀ´ÈÃÎÒ¿´¿´£¬ÈÃÎÒ³¤³¤¼ûʶ
ÒѾÓÐ6È˻ظ´
ÊÛSCIÎÄÕ£¬ÎÒ:8O5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼±
ÒѾÓÐ4È˻ظ´
ÃæÉϺÏ×÷µ¥Î»¸ÇÕÂ
ÒѾÓÐ5È˻ظ´
µ¼Ê¦Í²ۣºÎÒÔõô̯ÉÏÁËÕâô¸ö¼«Æ·Ñо¿Éú£¡
ÒѾÓÐ7È˻ظ´
ÉêÇëɾ³ý±¾Ìû
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¸ß·Ö×Ó²ÄÁϸÄÐÔÑз¢ÇóÖú¡¡
ÒѾÓÐ3È˻ظ´
±¨ÃûÇó¾È£¬¼±¼±¼±
ÒѾÓÐ4È˻ظ´
¹Ç¿Æ·½ÃæÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ11È˻ظ´
Çó½âÊý¾Ý£¬Ë®Æ½ÓÐÏ޸㲻ÏÂÈ¥ÁË
ÒѾÓÐ5È˻ظ´
podÊý¾Ý´¦ÀíÇóÖú
ÒѾÓÐ12È˻ظ´
ÇóÖú¸÷λ´óÏÀ ´óʦ ¿ìÀ´°ï°ïæ СŮ×Ó²»Ê¤¸Ð¼¤°¡ £¡£¡£¡
ÒѾÓÐ5È˻ظ´
Çó¼«ÖµÎÊÌâ¡£¼±¼±¼±
ÒѾÓÐ4È˻ظ´
Çó´óÅ£½âºË´ÅÆ×ͼ
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú¦Á-¼×»ù±½ÒÒÏ©Óë¹ýÁ¿±½·ÓÔÚÁòËá¼ÓÈÈÌõ¼þÏ·¢Éúʲô·´Ó¦£¿
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúTGÆ×·ÖÎö£¬¼±¼±¼±£¡
ÒѾÓÐ7È˻ظ´
΢Æ×ÇóÖú£¬¼±¼±¼±£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡ÔõôÎÒµÄÇóÖúÌûûÈ˻ظ´ÄØ£¬ÓÐÖØ½ð°¡£¡
ÒѾÓÐ15È˻ظ´
΢Æ×ÇóÖú£¡£¡£¡¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
OK,Äãµ½µ×O²»OK£¿
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖúµç»¯Ñ§×迹Æ×·ÖÎö£¬¼±¼±¼±
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇëÎÊÕâ¸öÆ×ͼÔõô»áÕâÑù£¿¼±¼±¼±£¡
ÒѾÓÐ10È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48833.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-12-03 10:49:40
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¿ÓµùÒ©»¯: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-12-03 10:49:40
|
²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . callistenone A C25H32O6 ÏàËÆ¶È:73.0% Tetrahedron 2013 69 6070-6075 Acylphloroglucinols from Callistemon lanceolatus DC. Suthida Rattanaburi, Wilawan Mahabusarakam, Souwalak Phongpaichit, Anthony R. Carroll Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . rhodomyrtosone I C28H30O6 ÏàËÆ¶È:57.6% Natural Product Research 2012 26 1904¨C1909 A new flavellagic acid derivative and phloroglucinol from Rhodomyrtus tomentosa A. Hiranrat, W. Chitbankluoi, W. Mahabusarakam, S. Limsuwan & S.P. Voravuthikunchai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . rhodomyrtone C26H34O6 ÏàËÆ¶È:57.6% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . rhodomyrtosone E C30H34O6 ÏàËÆ¶È:56.6% Bioorganic & Medicinal Chemistry Letters 2014 24 3096-3099 Chemical constituents from Eucalyptus citriodora Hook leaves and their glucose transporter 4 translocation activities Chao Wang, Jing Yang, Ping Zhao, Qi Zhou, Zhinan Mei, Guangzhong Yang, Xinzhou Yang, Yunjiang Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-cyclohexene-1,3-dioxo-5-hydroxy-2,2,6,6-tetramethyl-4-{1-[2,6-dihydroxy-4-methoxy-3-(3-methyl-l-oxo-butyl)phenyl]-3-methylbutyl} C27H38O7 ÏàËÆ¶È:55.5% Journal of Natural Products 1992 Vol 55 43 Antiviral Phloroglucinols from New Zealand Kunzea Species Stephen J. Bloor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . rhodomyrtone C26H34O6 ÏàËÆ¶È:53.8% Australian Journal of Chemistry 2002 55 229-232 Rhodomyrtone, an antibotic from Rhodomyrtus tomentosa Dachriyanus Salni, M. V. Sargent , B. W. Skelton, I. Soediro, M. Sutisna, A. H. White and E. Yulinah Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . antiarone C C26H30O6 ÏàËÆ¶È:53.8% Heterocycles 1990 31 1315-1324 Seven Prenylphenols, Antiarones C, D, E, F, G, H, and I from the Root Bark of Antiaris toxicaria Lesch. Yoshio Hano, Pedro Mitsui, and Taro Nomura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . rhodomyrtosone B C26H34O6 ÏàËÆ¶È:53.8% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . gambogenone C27H32O6 ÏàËÆ¶È:51.8% Journal of Natural Products 2005 68 354-360 Bioactive Benzophenones from Garcinia xanthochymus Fruits Scott Baggett, Petr Protiva, Eugene P. Mazzola, Hui Yang, Elizabeth T.Ressler, Margaret J. Basile, I. Bernard Weinstein, and Edward J. Kennelly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 12 C32H33O8Br ÏàËÆ¶È:51.8% Tetrahedron 2008 64 2192-2197 Isolation and characterization of two new drimanes from Zygogynum baillonii and synthesis of analogues Dalia Fomekong Fotsop, Fanny Roussi, Catherine Le Callonec, Hadjira Bousserouel, Marc Litaudon, Françoise Gu¨¦ritte Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . corymbone A C35H38O7 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(5) 881-883 Corymbones A and B, Phloroglucinols with Thyrotropin Releasing Hormone Receptor 2 Binding Affinity from the Flowers of Corymbia peltata Anthony R. Carroll, Sylvia Urban, Jasmine Lamb, Roger Moni,Gordon P. Guymer, Paul I. Forster, and Ronald J. Quinn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . isolupinisoflavone E C25H26O7 ÏàËÆ¶È:50% Journal of Natural Products 1997 60 292-293 Two New Isoflavones from the Bark of Ficus microcarpa Yen-Cheng Li and Yueh-Hsiung Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Hydroxyartocarpin C26H28O7 ÏàËÆ¶È:50% Journal of Natural Medicines 2010 64 478-481 Prenylated flavones from Artocarpus altilis Shireen Shaharina Shamaun, Mawardi Rahmani, Najihah Mohd Hashim, Hazar Bebe Mohd Ismail and Mohd Aspollah Sukari, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-amino-4-(4-methoxyphenyl)-2-phenylsulfanyl-6,7,8,9-tetra-hydrobenzo[1,8]-naphthyridine-3-carbonitrile C26H22N4OS ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2011 48 397-402 Microwave-assisted expeditious synthesis of novel benzo[1,8]-naphthyridine-3-carbonitriles Satish Kumar Singh and Krishna Nand Singh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . callistenone C C25H34O7 ÏàËÆ¶È:50% Tetrahedron 2013 69 6070-6075 Acylphloroglucinols from Callistemon lanceolatus DC. Suthida Rattanaburi, Wilawan Mahabusarakam, Souwalak Phongpaichit, Anthony R. Carroll Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 5-hydroxy-2,2,6,6-tetramethyl-4-(3-methyl-1-(2,4,6-trihydroxy-3-(3-methylbutanoyl)phenyl)butyl)cyclo-hex-4-ene-1,3-dione C26H36O7 ÏàËÆ¶È:50% Tetrahedron 2013 69 8559-8563 Synthesis of the acylphloroglucinols rhodomyrtone and rhodomyrtosone B Marius Morkunas, Linda Dube, Friedrich Götz, Martin E. Maier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-{1-{3-{[4-(Dibenzylamino) butyl]amino)propyl]piperidin-2-yl}-11-hydroxyundecan-1-one ÏàËÆ¶È:50% Helvetica Chimica Acta 1996 79 1379-1386 Synthesis of Oncinotin-11-one, a Macrocyclic Polyamine Alkaloid from Oncinotis tenuiloba Martin K.-H. Doll, Armin Guggisberg and Manfred Hesse Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-12-03 08:16:35









»Ø¸´´ËÂ¥
30