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[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.

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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