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1 .     1,2-seco-trypacidin
    ÏàËÆ¶È:100%
Chinese Journal of Natural Medicines          2005          3          269-271
Secondary Metabolites of Aspergillus fumigatus var. fumigatus
LU Chun-Hua; HUANG Yao-Jian; SHEN Yue-Mao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     monomethylsulochrin
    ÏàËÆ¶È:100%
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
3 .     sulochrin
C17H16O7     ÏàËÆ¶È:72.2%
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
4 .     Sulochrin
C17H16O7     ÏàËÆ¶È:72.2%
Bioscience, Biotechnology, and Biochemistry          2003          67          442-444
Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp.
Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     sulochrin
C17H16O7     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
6 .     sulochrin
    ÏàËÆ¶È:72.2%
The Journal of Antibiotics          1997          50          972-974
Sulochrin Inhibits Eosinophil Degranulation
HIROSHI OHASHI, MASAHARU ISHIKAWA, JUNKO ITO, AKIHIRO UENO, GERALD J. GLEICH, HIROHITO KITA, HIROYUKI KAWAI, HIROMI FUKAMACHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate
C17H16O7     ÏàËÆ¶È:72.2%
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
8 .     Hydroxysulochrin
C17H16O8     ÏàËÆ¶È:66.6%
Bioscience, Biotechnology, and Biochemistry          2003          67          442-444
Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp.
Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2013          96          458-462
Two New Secoanthraquinone Derivatives from the Marine-Derived Endophytic Fungus Aspergillus wentii EN-48
Hao-Fen Sun, Xiao-Ming Li, Ling-Hong Meng, Chuan-Ming Cui, Shu-Shan Gao, Chun-Shun Li and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     dinklagin C
C20H18O6     ÏàËÆ¶È:55.5%
Phytochemistry          2002          61          99-104
Dinklagins A, B and C: three prenylated flavonoids and other constituents from the twigs of Dorstenia dinklagei
Bonaventure T. Ngadjui, Etienne Dongo, Berhanu M. Abegaz,Serge Fotso, Helene Tamboue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 3
C18H16O7     ÏàËÆ¶È:55.5%
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
12 .     Compound 3
C18H16O7     ÏàËÆ¶È:55.5%
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
13 .     mucodianin B
C16H14O5     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          2010          58          254-256
A Novel 3-Arylcoumarin and Three New 2-Arylbenzofurans from Mucuna birdwoodiana
Ting Gong, Dong-Xiao Wang, Yan Yang, Ping Liu, Ruo-Yun Chen and De-Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 4
    ÏàËÆ¶È:55.5%
Tetrahedron Letters          2000          41          465-469
Studies toward the total synthesis of Sch 202596, an antagonist of the galanin receptor subtype GalR1: synthesis of geodin, the spirocoumaranone subunit of Sch 202596
Tadashi Katoh, Osamu Ohmori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 8d/1
C19H18ClN5O2     ÏàËÆ¶È:55.5%
Journal of Heterocyclic Chemistry          2004          41          915-929
Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol
Ibolya Prauda,M¨¢ria T¨®th-Lauritz and J¨®zsef Reiter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 8d/3
C20H21N5O3     ÏàËÆ¶È:55.5%
Journal of Heterocyclic Chemistry          2004          41          915-929
Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol
Ibolya Prauda,M¨¢ria T¨®th-Lauritz and J¨®zsef Reiter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1,7,9-trimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one
C17H16O5     ÏàËÆ¶È:55.5%
Heterocycles          2007          74          265-271
Synthesis of Alternariol through an Intramolecular Biaryl Coupling Reaction Using Palladium Reagent
Hitoshi Abe, Tomoko Fukumoto, Yasuo Takeuchi, and Takashi Harayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-07-23 15:23:17
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangwang1989

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

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ѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     1,2-seco-trypacidin
    ÏàËÆ¶È:100%
Chinese Journal of Natural Medicines          2005          3          269-271
Secondary Metabolites of Aspergillus fumigatus var. fumigatus
LU Chun-Hua; HUANG Yao-Jian; SHEN Yue-Mao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     monomethylsulochrin
    ÏàËÆ¶È:100%
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
3 .     sulochrin
C17H16O7     ÏàËÆ¶È:72.2%
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
4 .     Sulochrin
C17H16O7     ÏàËÆ¶È:72.2%
Bioscience, Biotechnology, and Biochemistry          2003          67          442-444
Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp.
Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     sulochrin
C17H16O7     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
6 .     sulochrin
    ÏàËÆ¶È:72.2%
The Journal of Antibiotics          1997          50          972-974
Sulochrin Inhibits Eosinophil Degranulation
HIROSHI OHASHI, MASAHARU ISHIKAWA, JUNKO ITO, AKIHIRO UENO, GERALD J. GLEICH, HIROHITO KITA, HIROYUKI KAWAI, HIROMI FUKAMACHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate
C17H16O7     ÏàËÆ¶È:72.2%
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3Â¥2013-07-23 15:24:18
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