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23.27,52.90,56.18,56.84,84.14,104.04,105.46,105.65,108.41,137.20,138.35,152.26,158.42,163.58,169.58,174.45,185.74,190.58
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22.26,51.85,55.52,55.88,102.75,102.79,103.10,107.94,110.32,110.53,110.58,126.48,128.09,147.52,156.63,157.87,160.79,163.93,166.20,199.87
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2Â¥: Originally posted by sdrlcw at 2013-07-26 15:46:35
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BIS-DECHLORO-GEODIN
J.ANTIBIOTICS,49,1056(1996)
Y.TANAKA,K.MATSUZAKI,C.L.ZHONG,H.YOSHIDA,T.KAWAKUBO,R.MASUMA,H.TANAKA,S.OMURA

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1 .     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 .     bis-dechlorogeodin
C17H14O7     ÏàËÆ¶È:61.1%
The Journal of Antibiotics          1996          49          1056-1059
Dechlorogeodin and Its New Dihydro Derivatives, Fungal Metabolites with Herbicidal Activity
YOSHITAKE TANAKA, KEIICHI MATSUZAKI, CHONG-LIN ZHONG, HIROSHI YOSHIDA, TOMOYA KAWAKUBO, ROKURO MASUMA, HARUO TANAKA, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 12
C19H18O8     ÏàËÆ¶È:52.6%
Tetrahedron          2012          68          4107-4111
Chemical synthesis of funicone analogs
Emiliano Manzo, Maria Letizia Ciavatta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     geodin
C17H12Cl2O7     ÏàËÆ¶È:50%
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
5 .     quinquangulin
C16H14O5     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          1153-1156
A New Naphthopyrone Derivative from Cassia quinquangulata and Structural Revision of Quinquangulin and Its Glycosides
Xing-Cong Li, D. Chuck Dunbar, Hala N. ElSohly, Melissa R. Jacob, Alison C. Nimrod,Larry A. Walker, and Alice M. Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     nidulalin A
C16H14O6     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1994          42          1720-1723
Structures of a New Dihydroxanthone Derivative, Nidulalin A, and a New Benzophenone Derivative, Nidulalin B, from Emericella nidulans
Nobuo KAWAHARA,Setsuko SEKITA,Motoyoshi SATAKE,Shun-ichi UDAGAWA and Ken-ichi KAWAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     nidulalin A
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1998          46          1506-1510
Manoamine Oxidase Inhibitory constituents from Anixiella micropertusa
Haruhiro FUJIMOTO,Yoko SATOH,Kentaro YAMAGUCHI and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1-hydroxy-3,6,7-trimethoxyxanthone acetate
C18H16O7     ÏàËÆ¶È:50%
Phytochemistry          1991          30          2061-2065
Two xanthones from Polygala tenuifolia
Yukinobu Ikeya, Kô Sugama, Minoru Okada, Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gonytolide C
C16H16O7     ÏàËÆ¶È:50%
Organic Letters          2011          Vol. 13, No. 17          4624-4627
Structures of the Dimeric and Monomeric Chromanones, Gonytolides A C, Isolated from the Fungus Gonytrichum sp. And Their Promoting Activities of Innate Immune Responses
Haruhisa Kikuchi, Masato Isobe, Mizuki Sekiya, Yuko Abe, Tsuyoshi Hoshikawa,Kazunori Ueda, Shoichiro Kurata, Yasuhiro Katou, and Yoshiteru Oshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (¡À)-geodin
    ÏàËÆ¶È:50%
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
11 .     1,7,9-trimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one
C17H16O5     ÏàËÆ¶È:50%
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
12 .     Compound 21
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2000          10          1755-1757
Diels¨Calder approach to tetralin-based constrained ¦Á-amino acid derivatives
Sambasivarao Kotha, Thota Ganesh, Arun Kumar Ghosh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     2-(3'-chloro-4'-hydroxy-2'-methoxy-6'-methoxycarbonylphenoxy)-6-hydroxy-4-methylbenzoic acid
C17H15O8Cl     ÏàËÆ¶È:50%
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
14 .     dechlorodihydromaldoxin
C17H16O8     ÏàËÆ¶È:50%
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
15 .     (+)-geodin
    ÏàËÆ¶È:50%
The Journal of Antibiotics          2005          58          583-589
Identification and Preliminary SAR Studies of (+)-Geodin as a Glucose Uptake Stimulator for Rat Adipocytes FREE
Seiichi Sato, Noriyuki Okusa, Akiyo Ogawa, Takao Ikenoue, Tetsuya Seki and Takashi Tsuji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     5,3',4'-trihydroxy-6,7,5'-trimethoxyflavone
    ÏàËÆ¶È:50%
Biological and Pharmaceutical Bulletin          2002          25          875-879
Antiproliferative Constituents in Plants 10. Flavones from the Leaves of Lantana montevidensis BRIQ. and Consideration of Structure¨CActivity Relationship
Tsuneatsu Nagao, Fumiko Abe, Junei Kinjo, Hikaru Okabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
4Â¥2013-07-26 15:51:53
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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²éѯ½á¹û£º¹²²éµ½43¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     1,2-seco-trypacidin
    ÏàËÆ¶È:90%
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:75%
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:65%
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
4 .     sulochrin
C17H16O7     ÏàËÆ¶È:65%
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
5 .     methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate
C17H16O7     ÏàËÆ¶È:65%
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
6 .     Hydroxysulochrin
C17H16O8     ÏàËÆ¶È:60%
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
7 .     sulochrin
    ÏàËÆ¶È:60%
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
8 .     sulochrin
C17H16O7     ÏàËÆ¶È:55%
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
9 .     compound 3c
    ÏàËÆ¶È:55%
Journal of Natural Products          1979          Vol 42          264-270
Two New C-Benzylated Flavanones From Uvaria chamae and 13C NMR Analysis of Flavanone Methyl Ethers
Hala N. El-Sohly, William L. Lasswell Jr., Charles D. Hufford
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 4
    ÏàËÆ¶È:55%
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
11 .     1-benzyloxy-7,9-dimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one
C23H20O5     ÏàËÆ¶È:55%
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
12 .     Sulochrin
C17H16O7     ÏàËÆ¶È:55%
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   Ì¼Æ×Ä£Äâͼ
13 .     6-hydroxyl-deoxyfunicone
C19H18O8     ÏàËÆ¶È:55%
Phytochemistry Letters          2013          6          14-17
Metabolites from Penicillium sp., an endophytic fungus from the liverwort Riccardia multifida (L.) S. Gray
Yang Jiao, Xin Zhang, Lei Wang, Gang Li, Jin-Chuan Zhou, Hong-Xiang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     methyl asterrate
    ÏàËÆ¶È:55%
Chinese Journal of Natural Medicines          2012          10          36-39
Chemical constituents of Allophylus longipes
Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid
    ÏàËÆ¶È:55%
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
16 .     1-(2-Hydroxy-6-methoxyphenyl)-1,3-butanedione
C11H12O4     ÏàËÆ¶È:54.5%
Tetrahedron          2012          68          6948-6956
Access to 2-alkyl chromanones via a conjugate addition approach
Louise A. Stubbing, Freda F. Li, Daniel P. Furkert, Vittorio E. Caprio, Margaret A. Brimble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Compound 5
C21H19NO6     ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry Letters          2005          15          2795-2798
Dihydroindenoisoquinolines function as prodrugs of indenoisoquinolines
Xiangshu Xiao, Ze-Hong Miao, Smitha Antony, Yves Pommier, Mark Cushman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     N-((R)-2-(5-chloro-2-(4-methoxypyridin-2-yl)-6-methylpyrimidin-4-ylamino)-1-phenylethyl)-4-(piperazin-1-yl)butanamide
C27H34ClN7O2     ÏàËÆ¶È:52.1%
Bioorganic & Medicinal Chemistry          2013          21          2600-2617
Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1
Pengtao Zhang, Xinye Yang, Feiran Zhang, Sandra B. Gabelli, Renxiao Wang, Yihua Zhang, Shridhar Bhat, Xiaochun Chen, Manuel Furlani, L. Mario Amzel, Jun O. Liu, Dawei Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     disparacetylfuran A
C24H20O6     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          563-568
Novel Cytotoxic 4-Phenylfuranocoumarins from Calophyllum dispar
David Guilet,Jean-Jacques H¨¦lesbeux, Denis S¨¦raphin,Thierry S¨¦venet, Pascal Richomme, and Jean Bruneton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     2-methoxygliricidol
C18H16O7     ÏàËÆ¶È:50%
Journal of Natural Products          1999          62          188-190
New 12a-Hydroxyrotenoids from Gliricidia sepium Bark
Luca Rastrelli, Ingeborg Berger, Wolfang Kubelka, Armando Caceres, Nunziatina De Tommasi, and Francesco De Simone
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     cercophorin C
C20H16O10     ÏàËÆ¶È:50%
Journal of Natural Products          1996          59          765-769
Cercophorins A-C: Novel Antifungal and Cytotoxic Metabolites from the Coprophilous Fungus Cercophora areolata
Authrine C. Whyte and James B. Gloer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
6Â¥2013-07-26 15:53:29
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