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13C NMR (126 MHz, dmso) ¦Ä20.99,52.6,56.45,103.91,107.73,108.9,110.49,110.81,126.02,128.41,145.01,157.24,158.84,166.06,200.45
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·ÉÏèµÄ¶À½ÇÊÞ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ÒѶԳöлл~ 2015-03-12 10:28:21
.     sulochrin
C17H16O7     ÏàËÆ¶È:80%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Sulochrin
C17H16O7     ÏàËÆ¶È:80%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     sulochrin
C17H16O7     ÏàËÆ¶È:80%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     sulochrin
    ÏàËÆ¶È:80%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     Hydroxysulochrin
C17H16O8     ÏàËÆ¶È:73.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     methyl 6-acetyl-4-methoxy-5,7,8-trihydroxynaphthalene-2-carboxylate
    ÏàËÆ¶È:73.3%
Electronic Journal of Biotechnology          2009          12          1-9
Novel antimicrobial secondary metabolites from a Penicillium sp. isolated from Brazilian cerrado soil
Philippe Petit,Esther M. F. Lucas,Lucas M. Abreu,Ludwig H. Pfenning,Jacqueline A. Takahashi*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate
C17H16O7     ÏàËÆ¶È:70.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Sulochrin
C17H16O7     ÏàËÆ¶È:66.6%
Russian Chemical Bulletin          2011          60          760-763
4-Methoxy-3-methylgoniothalamin from marine-derived fungi of the genus Penicillium
O. F. Smetanina, A. N. Yurchenko, A. I. Kalinovsky, M. A. Pushilin and N. N. Slinkina, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     1,2-seco-trypacidin
    ÏàËÆ¶È:61.1%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     monomethylsulochrin
    ÏàËÆ¶È:61.1%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     6-methyl-anthragallol-2-methyl ether
C16H12O5     ÏàËÆ¶È:56.2%
Natural Product Sciences          2004          10          63-68
Anthraquinones with Antibacterial Activities from Crucianella maritima L. Growing in Egypt
El-Lakany, Abdalla M.; Aboul-Ela, Maha A.; Abdel-Kader, Maged S.; Badr, Jihan M.; Sabri, Nawal N.; Goher, Yousry
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid
    ÏàËÆ¶È:56.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     1,4,5-trihydroxy-7-methoxy-2-methyl-anthraquinone
    ÏàËÆ¶È:56.2%
Phytotherapy Research          2014          28          774−780
Anti-leishmanial Activities of Extracts and Isolated Compounds from Drechslera rostrata and Eurotium tonpholium
Amani S. Awaad, Haifa M. Al-Zaylaee, Saleh I. Alqasoumi, Mohamed E. Zain, Ebtesam M. Aloyan, Ahmed M. Alafeefy, Elham S. H. Awad and Reham M. El-Meligy
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     monom ethyl sulochrin
C18H18O7     ÏàËÆ¶È:55.5%
Chinese Journal of New Drugs          2010          19          1402-1406
Identification of endophytic fungi SIPI3.0550 and its metabolites
ZHANG Zhi-jie, QU Ling-bo, ZHOU Yu-meng, LI Ji-an, SHAO Lei, CHEN Dai-jie
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     monomethylsulochrin
    ÏàËÆ¶È:55.5%
Chemistry of Natural Compounds          2014          50          526-528
Antimicrobial Metabolites from the Endophytic Fungus Aspergillus sp. of Eucommia ulmoides
Hongchi Zhang, Rui Liu, Feng Zhou, Runmei Wang, Xiaocui Liu, Hangtao Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     6-hydroxymethyleugenin
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1681-1682
The Isolation of Two New Chromone Derivatives from the New Zealand Fungus Tolypocladium extinguens
Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     compound 4
    ÏàËÆ¶È:53.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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