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1 .     neoplaether
    ÏàËÆ¶È:88.8%
FEMS Microbiology Letters          2006          261          218-223
Neoplaether, a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016
Feng W. Wang, Yong H. Ye, Jing R. Chen, Xiao T. Wang, Hai L. Zhu, Yong C. Song and Ren X. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     methyl asterric acid
C18H8O8     ÏàËÆ¶È:77.7%
The Journal of Antibiotics          2002          55          552-556
Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs
HEE JUNG LEE,JEONG HYEONG LEE,BANG YEON HWANG,HANG SUB KIM and JUNG JOON LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     dimethyl 2,3'-dimethoxyosoate
C19H20O8     ÏàËÆ¶È:73.6%
The Journal of Antibiotics          2006          59          362-365
A New Diphenyl Ether from Marine-derived Fungus Aspergillus sp. B-F-2 FREE
Rui Liu, Weiming Zhu, Yapeng Zhang, Tianjiao Zhu, Hongbing Liu, Yuchun Fang and Qianqun Gu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 3
C18H16O7     ÏàËÆ¶È:72.2%
Records of Natural Products          2012          6:1          28-34
Secondary Metabolites of Aspergillus sp. CM9a, an Endophytic Fungus of Cephalotaxus mannii
Heng Xue, Chunhua Lu, Lanying Liang and Yuemao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Compound 3
C18H16O7     ÏàËÆ¶È:72.2%
Records of Natural Products          2012          6          28-34
Secondary Metabolites of Aspergillus sp. CM9a,an Endophytic Fungus of Cephalotaxus mannii
Heng Xue,Chunhua Lu,Lanying Liang and Yuemao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-chloroasterric acid
C18H17ClO8     ÏàËÆ¶È:72.2%
The Journal of Antibiotics          2002          55          552-556
Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs
HEE JUNG LEE,JEONG HYEONG LEE,BANG YEON HWANG,HANG SUB KIM and JUNG JOON LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     methyl-2-[1-(3,4,5-trimethoxyphenyl)vinyl]benzofuran-5-carboxylate
C21H20O6     ÏàËÆ¶È:61.1%
European Journal of Organic Chemistry          2011                   4868-4876
Synthesis of 2-(1-Phenylvinyl)benzofurans and 2-(1-Phenylvinyl)indoles as Antimitotic Agents by a Tandem Palladium-Assisted Coupling-Cyclization Reaction between 1-Phenylvinyl Iodides and ortho-Substituted Arylalkynes
Bret Tr¨¦guier, Evelia Rasolofonjatovo, Abdallah Hamze, Olivier Provot, Joanna Wdzieczak-Bakala, Joëlle Dubois, Jean-Daniel Brion and Mouad Alami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     asterric acid
C17H16O8     ÏàËÆ¶È:61.1%
Natural Product Research          2012          26          1224-1228
A new diphenyl ether from Phoma sp. strain, SHZK-2
M.J. Fang, H. Fang, W.J. Li, D.M. Huang, Z. Wu & Y.F. Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     methyl asterrate
C18H18O8     ÏàËÆ¶È:55.5%
Journal of Natural Products          2002          65          7-10
New Chlorinated Diphenyl Ethers from an Aspergillus Species
Jaih Hargreaves, Ja-on Park, Emilio L. Ghisalberti, Krishnapillai Sivasithamparam, Brian W. Skelton, and Allan H. White
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     krametosan
C17H14O5     ÏàËÆ¶È:55.5%
Natural Product Research          2001          15          323-329
Kramentosan, a New Trinorlignan from the Roots of Krameria tomentosa
Samia A. S. Silva; Janiza C. M. De Castro; Terezinha G. Da Silva; Emidio V. L. Da-cunha; Jos¨¦ Maria Barbosa-Filho; Marcelo S. Da Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     dechlorodihydromaldoxin
C17H16O8     ÏàËÆ¶È:55.5%
Journal of the Chemical Society, Perkin Transactions 1          1996                   1419-1425
Metabolites of the higher fungi. Part 29. Maldoxin, maldoxone, dihydromaldoxin, isodihydromaldoxin and dechlorodihydromaldoxin. A spirocyclohexadienone, a depsidone and three diphenyl ethers: keys in the depsidone biosynthetic pathway from a member of the
Monilola O. Adeboya, Raymond L. Edwards, Thomas Lassøe, Derek J. Maitland, Len Shields and Anthony J. S. Whalley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     6-amino-5-{[(1E)-(2,4,6-trimethoxyphenyl)methylene]-amino}-1-[(4-methylphenyl) sulfonyl]-2-oxo-1,2-dihydropyri-midine-4-carbonitrile
C22H21N5O6S     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2010          18          7639-7650
A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors
Abdel-Sattar S. Hamad Elgazwy, Nasser S.M. Ismail, Heba S.A. Elzahabi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     methyl asterrate
C18H18O8     ÏàËÆ¶È:55.5%
Natural Product Research          2012          26          1224-1228
A new diphenyl ether from Phoma sp. strain, SHZK-2
M.J. Fang, H. Fang, W.J. Li, D.M. Huang, Z. Wu & Y.F. Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     trans-2-[3-(3,4,5-trimethoxyphenylpropenoyl)amino]-3,5-dimethoxybenzoic acid methyl ester
C22H25NO8     ÏàËÆ¶È:55%
Journal of Natural Products          1994          Vol 57          90
Isolation, Identification, and Synthesis of Miriamides, New Hostmarkers from Eggs of Pieris brassicae
Anton Blaakmeer, Andr¨¦ Stork, Albertus van Veldhuizen, Teris A. van Beek, Aede de Groot, Joop J. A. van Loon, Louis M. Schoonhoven
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     conyzatin
    ÏàËÆ¶È:55%
Phytochemistry          1985          24          835-848
Chemistry of toxic range plants. Highly oxygenated flavonol methyl ethers from Gutierrezia microcephala
James N. Roitman, Lynn F. James
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ethyl asterrate
C19H20O8     ÏàËÆ¶È:52.6%
Journal of Natural Products          2008          71(9)          1643-1646
Bioactive Asterric Acid Derivatives from the Antarctic Ascomycete Fungus Geomyces sp.
Yan Li, Bingda Sun, Shuchun Liu, Lihua Jiang, Xingzhong Liu, Hua Zhang, and Yongsheng Che
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 3
C20H22O7     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          1981          29          1000-1004
The Glycosides of Plantago major var. japonica NAKAI. A New Flavanone Glycoside, Plantagoside
TOHRU ENDO,HEIHACHIRO TAGUCHI and ITIRO YOSIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Ethyl 1-(3,4,5-trimethoxyphenylcarbonylamino)-4-oxo-4H-quinolizine-3-carboxylate
    ÏàËÆ¶È:52.6%
Molecules          2009          14          868-883
Design, Synthesis and Anti-HIV Integrase Evaluation of 4-Oxo-4H-quinolizine-3-carboxylic Acid Derivatives
Yi-Sheng Xu, Cheng-Chu Zeng, Zi-Guo Jiao, Li-Ming Hu and Ru-gang Zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     methyl 2,4-dichloroasterrate
    ÏàËÆ¶È:52.6%
Natural Product Research          2009          23          77-85
Secondary metabolites of Aspergillus sp. F1, a commensal fungal strain of Trewia nudiflora
Ting Lin; Chunhua Lu; Yuemao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     erianin acetate
    ÏàËÆ¶È:52.6%
Phytochemistry          1999          52          1365-1369
Bibenzyl derivatives from the orchid Dendrobium amoenum
P.L Majumder, S. Guha, S. Sen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     akuammigine
    ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli, Gianluca Nasini, Felix W. Wehrli, Edward W. Hagaman and Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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