| ²é¿´: 323 | »Ø¸´: 1 | |||
yetta_he½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CDCL3 20.69,55.13,55.91,56.21,62.02,84.82,87.54,87.60,92.38,96.49,96.86,101.20,101.34,107.37,107.40,153.35,155.38,158.62,161.37,162.16,162.71,167.55,167.63,183.04,184.43,184.56,184.59,184.66,184.75,185.06. ¸Ðл~~ |
» ²ÂÄãϲ»¶
293µ÷¼Á
ÒѾÓÐ25È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ20È˻ظ´
336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ25È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
309Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
È˹¤ÖÇÄÜ320µ÷¼Á08¹¤À໹Óлú»áÂð
ÒѾÓÐ4È˻ظ´
ɽ¶«Ê¡»ù½ð2026
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
¿û»¨ÅɸßÊÖ
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 40 (СѧÉú)
- ½ð±Ò: 29.8
- É¢½ð: 20
- ºì»¨: 2
- Ìû×Ó: 229
- ÔÚÏß: 99.8Сʱ
- ³æºÅ: 2513202
- ×¢²á: 2013-06-19
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yetta_he: ½ð±Ò+8, ¡ïÓаïÖú 2015-01-22 16:53:23
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yetta_he: ½ð±Ò+8, ¡ïÓаïÖú 2015-01-22 16:53:23
|
1 . aurasperone A C32H26O10 ÏàËÆ¶È:62.5% 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 ̼Æ×Ä£Äâͼ 2 . aurasperone A ÏàËÆ¶È:62.5% 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 ̼Æ×Ä£Äâͼ 3 . isoaurasperone A ÏàËÆ¶È:62.5% 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 ̼Æ×Ä£Äâͼ 4 . asperpyrone C C32H26O10 ÏàËÆ¶È:59.3% 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 ̼Æ×Ä£Äâͼ 5 . aurasperone A C32H26O10 ÏàËÆ¶È:59.3% 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 ̼Æ×Ä£Äâͼ 6 . asperpyrone D C31H24O10 ÏàËÆ¶È:56.6% 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 ̼Æ×Ä£Äâͼ 7 . fonsecinone A C32H26O10 ÏàËÆ¶È:56.2% 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 ̼Æ×Ä£Äâͼ 8 . asperpyrone C ÏàËÆ¶È:56.2% 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 ̼Æ×Ä£Äâͼ 9 . 8'-O-demethylnigerone C31H24O11 ÏàËÆ¶È:54.8% 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 ̼Æ×Ä£Äâͼ 10 . isonigerone ÏàËÆ¶È:54.8% 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 ̼Æ×Ä£Äâͼ |

2Â¥2015-01-22 16:04:38













»Ø¸´´ËÂ¥