| ²é¿´: 422 | »Ø¸´: 1 | |||
ÐĵÄ×·ÖðÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖúM-1 ÒÑÓÐ1È˲ÎÓë
|
|
1.2,21.0,55.3,56.1,62.2,96.6,97,101.4,101.5,104.4,104.9,105.3,107.4,107.6,108.7,111.6,117.7,140.7,140.8,151.0,153.5,158.7,160.3,161.2,161.5,162.1,162.8,167.7,167.8,184.6,184.7 ÈܼÁÊÇë®´úÂÈ·Â ÏàËÆ¶È´óÓÚ60% |
» ²ÂÄãϲ»¶
266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ16È˻ظ´
Çóµ÷¼Á£º085600²ÄÁÏÓ뻯¹¤£¬¿¼²Ä¿Æ»ù£¬×Ü·Ö319
ÒѾÓÐ22È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085701Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ3È˻ظ´
0710ÉúÎïѧ336·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
µç×ÓÐÅÏ¢µ÷¼Á½»²æÑ§¿ÆÓÐÍÆ¼öÂð
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
280Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл~
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö!
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ìáǰлл£¡
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý,ǰ10¸ö¼´¿É
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´

÷´º
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 242 (´óѧÉú)
- ½ð±Ò: 1940.6
- É¢½ð: 48
- ºì»¨: 3
- Ìû×Ó: 465
- ÔÚÏß: 121.1Сʱ
- ³æºÅ: 1536801
- ×¢²á: 2011-12-14
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÐĵÄ×·Öð: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-06 19:49:36
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÐĵÄ×·Öð: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-06 19:49:36
|
1 . aurasperone A C32H26O10 ÏàËÆ¶È:93.7% Magnetic Resonance in Chemistry 2005 43 962-965 Complete 1H and 13C NMR assignments of aurasperone A and fonsecinone A, two bis-naphthopyrones produced by Aspergillus aculeatus Francinete Ramos Campos, Andersson Barison, Cristina Daolio, Antonio G. Ferreira and Edson Rodrigues-Fo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . aurasperone A ÏàËÆ¶È:93.7% Natural Product Research and Development 2014 26 517-520 Dimeric Naphthopyrones from Penicillium oxalicum,a Fungus Residing in Acrida cinerea XU Bang, ZOU Kun, GUO Lin-zhi, LIU Cheng-xiong, CHENG Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . isoaurasperone A ÏàËÆ¶È:93.7% Natural Product Research 2014 28 1388-1392 Antifungal and antibacterial metabolites from an endophytic Aspergillus sp. associated with Melia azedarach Jian Xiao, Qiang Zhang, Yu-Qi Gao, Xin-Wei Shi & Jin-Ming Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . asperpyrone D ÏàËÆ¶È:90.3% Natural Product Research and Development 2014 26 517-520 Dimeric Naphthopyrones from Penicillium oxalicum,a Fungus Residing in Acrida cinerea XU Bang, ZOU Kun, GUO Lin-zhi, LIU Cheng-xiong, CHENG Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . fonsecinone A C32H26O10 ÏàËÆ¶È:87.5% Magnetic Resonance in Chemistry 2005 43 962-965 Complete 1H and 13C NMR assignments of aurasperone A and fonsecinone A, two bis-naphthopyrones produced by Aspergillus aculeatus Francinete Ramos Campos, Andersson Barison, Cristina Daolio, Antonio G. Ferreira and Edson Rodrigues-Fo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . aurasperone A C32H26O10 ÏàËÆ¶È:87.5% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 113-115 Pyrones in Metabolites of Marine Mangrove Endophytic Fungus(No.ZZF79) from the South China Sea HUANG Zhong-jing, SHAO Chang-lun, CHEN Yi-guang, LIN Yong-cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . asperpyrone C ÏàËÆ¶È:87.5% Natural Product Research and Development 2014 26 517-520 Dimeric Naphthopyrones from Penicillium oxalicum,a Fungus Residing in Acrida cinerea XU Bang, ZOU Kun, GUO Lin-zhi, LIU Cheng-xiong, CHENG Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . asperpyrone C C32H26O10 ÏàËÆ¶È:84.3% Journal of Natural Products 2003 66 136-139 New Dimeric Naphthopyrones from Aspergillus niger Kohki Akiyama, Seigo Teraguchi, Yukiko Hamasaki, Mika Mori, Kunihiko Tatsumi, Kenji Ohnishi, and Hideo Hayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . asperpyrone A ÏàËÆ¶È:83.8% Natural Product Research and Development 2014 26 517-520 Dimeric Naphthopyrones from Penicillium oxalicum,a Fungus Residing in Acrida cinerea XU Bang, ZOU Kun, GUO Lin-zhi, LIU Cheng-xiong, CHENG Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 8'-O-demethylisonigerone C31H24O10 ÏàËÆ¶È:81.2% Chemistry & Biodiversity 2008 Vol. 5 93-100 Isolation, Structure Elucidation, and Antimycobacterial Properties of Dimeric Naphtho-g-pyrones from the Marine-Derived Fungus Aspergillus carbonarius YapengZhang, Sun Ling, YuchunFang, Tianjiao Zhu, Qianqun Gu and Wei-Ming Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 8'-O-demethylnigerone C31H24O11 ÏàËÆ¶È:80.6% Chemistry & Biodiversity 2008 Vol. 5 93-100 Isolation, Structure Elucidation, and Antimycobacterial Properties of Dimeric Naphtho-g-pyrones from the Marine-Derived Fungus Aspergillus carbonarius YapengZhang, Sun Ling, YuchunFang, Tianjiao Zhu, Qianqun Gu and Wei-Ming Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . isonigerone ÏàËÆ¶È:80.6% Chemistry & Biodiversity 2008 Vol. 5 93-100 Isolation, Structure Elucidation, and Antimycobacterial Properties of Dimeric Naphtho-g-pyrones from the Marine-Derived Fungus Aspergillus carbonarius YapengZhang, Sun Ling, YuchunFang, Tianjiao Zhu, Qianqun Gu and Wei-Ming Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . asperpyrone D C31H24O10 ÏàËÆ¶È:80.6% Phytochemistry 2007 68 368-372 Asperpyrone D and other metabolites of the plant-associated fungal strain Aspergillus tubingensis Jixun Zhan, G.M. Kamal B. Gunaherath, E.M. Kithsiri Wijeratne, A.A. Leslie Gunatilaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . asperpyrone B C32H26O10 ÏàËÆ¶È:75% Journal of Natural Products 2003 66 136-139 New Dimeric Naphthopyrones from Aspergillus niger Kohki Akiyama, Seigo Teraguchi, Yukiko Hamasaki, Mika Mori, Kunihiko Tatsumi, Kenji Ohnishi, and Hideo Hayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . asperpyrone B ÏàËÆ¶È:71.8% Natural Product Research and Development 2014 26 517-520 Dimeric Naphthopyrones from Penicillium oxalicum,a Fungus Residing in Acrida cinerea XU Bang, ZOU Kun, GUO Lin-zhi, LIU Cheng-xiong, CHENG Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . xanthoviridicatin F C27H20O9 ÏàËÆ¶È:64.5% Helvetica Chimica Acta 2003 Vol. 86 3380 Isolation, Structure, and HIV-1 Integrase Inhibitory Activity of Xanthoviridicatin E and F, Two Novel Fungal Metabolites Produced by Penicillium chrysogenum Sheo B. Singh, Deborah L. Zink, Ziqiang Guan, Javier Collado, Fernando Pelaez,Peter J. Felock, and Daria J. Hazuda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . planifolin C31H26O10 ÏàËÆ¶È:64.5% Journal of Natural Products 2001 64 122-124 Planifolin, a New Naphthopyranone Dimer and Flavonoids from Paepalanthus planifolius Lourdes C. Santos,Sonia Piacente, Cosimo Pizza, Klaus Albert, Markus Dachtler, and Wagner Vilegas Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . podocarpusflavone A C31H20O10 ÏàËÆ¶È:61.2% Acta Botanica Yunnanica 2005 27 107-110 Three Bioactive Biflavones Isolated from Taxodium mucronatum ZHANG Yu-Mei, TAN Ning-Hua, HUANG Huo-Qiang, JIA Rui-Rui, ZENG Guang-Zhi, JI Chang-Jiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-06 13:53:17














»Ø¸´´ËÂ¥
120