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1 .     viridicatumtoxin
    ÏàËÆ¶È:93.7%
The Journal of Antibiotics          2008          61          633-637
Viridicatumtoxin B, a new anti-MRSA agent from Penicillium sp. FR11
Chang-Ji Zheng, Hyung-Eun Yu, Eun-Hee Kim and Won-Gon Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     viridicatumtoxin
    ÏàËÆ¶È:93.7%
The Journal of Antibiotics          1993          46          214-221
ANTHROTAININ, AN INHIBITOR OF SUBSTANCE P BINDING PRODUCED BY Gliocladium catenulatum
SUI-MING WONG, RUDOLPH KULLNIG, JONAS DEDINAS, KENNETH C. APPELL, GWENDOLYN C. KYDD, AMANDA M. GILLUM, RAYMOND COOPER, RICHARD MOORE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     viridicatumtoxin
C30H31NO10     ÏàËÆ¶È:93.7%
The Journal of Antibiotics          2013          66          37-41
Spirohexalines, new inhibitors of bacterial undecaprenyl pyrophosphate synthase, produced by Penicillium brasilianum FKI-3368 FREE
Junji Inokoshi, Yuichiro Nakamura, Zhang Hongbin, Ryuji Uchida, Ken-ichi Nonaka, Rokuro Masuma and Hiroshi Tomoda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     viridicatumtoxin
    ÏàËÆ¶È:87.5%
Journal of Natural Products          1982          Vol 45          321-327
Microbial Transformations of Natural Antitumor Agents. 20. Glucosylation of Viridi-catumtoxin
M. S. Raju, G.-S. Wu, A. Gard, J. P. Rosazza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     spirohexaline
C31H32O10     ÏàËÆ¶È:84.3%
The Journal of Antibiotics          2013          66          37-41
Spirohexalines, new inhibitors of bacterial undecaprenyl pyrophosphate synthase, produced by Penicillium brasilianum FKI-3368 FREE
Junji Inokoshi, Yuichiro Nakamura, Zhang Hongbin, Ryuji Uchida, Ken-ichi Nonaka, Rokuro Masuma and Hiroshi Tomoda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     viridicatumtoxin B
C30H29NO10     ÏàËÆ¶È:62.5%
The Journal of Antibiotics          2008          61          633-637
Viridicatumtoxin B, a new anti-MRSA agent from Penicillium sp. FR11
Chang-Ji Zheng, Hyung-Eun Yu, Eun-Hee Kim and Won-Gon Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3-O-nicotinoyl-19-O-(4-methoxylbenzoyl)dehydroandrographolide
C34H37NO7     ÏàËÆ¶È:53.1%
Archiv der Pharmazie          2012          345          647-656
Synthesis and Biological Evaluation of Andrographolide Derivatives as Potent Anti-HIV Agents
Chunlei Tang, Yajuan Liu, Bin Wang, Guolong Gu, Liumeng Yang, Yongtang Zheng, Hai Qian and Wenlong Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     dichrostachine B
C36H40O9     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     dichrostachine C
C36H40O8     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     viridicatumtoxin
    ÏàËÆ¶È:50%
Journal of Natural Products          1982          Vol 45          321-327
Microbial Transformations of Natural Antitumor Agents. 20. Glucosylation of Viridi-catumtoxin
M. S. Raju, G.-S. Wu, A. Gard, J. P. Rosazza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     viridicatumtoxin-11-O-glucoside
    ÏàËÆ¶È:50%
Journal of Natural Products          1982          Vol 45          321-327
Microbial Transformations of Natural Antitumor Agents. 20. Glucosylation of Viridi-catumtoxin
M. S. Raju, G.-S. Wu, A. Gard, J. P. Rosazza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3-O-nicotinoyl-19-O-phenoxyacetyldehydroandrographolide
C34H37NO7     ÏàËÆ¶È:50%
Archiv der Pharmazie          2012          345          647-656
Synthesis and Biological Evaluation of Andrographolide Derivatives as Potent Anti-HIV Agents
Chunlei Tang, Yajuan Liu, Bin Wang, Guolong Gu, Liumeng Yang, Yongtang Zheng, Hai Qian and Wenlong Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-nicotinoyl-19-O-(2-nitrobenzoyl)-dehydroandrographolide
C33H34N2O8     ÏàËÆ¶È:50%
Archiv der Pharmazie          2012          345          647-656
Synthesis and Biological Evaluation of Andrographolide Derivatives as Potent Anti-HIV Agents
Chunlei Tang, Yajuan Liu, Bin Wang, Guolong Gu, Liumeng Yang, Yongtang Zheng, Hai Qian and Wenlong Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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