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MeOD  ¦Ä 162.28, 159.64, 159.58, 141.69, 112.83, 112.09, 111.73, 110.58, 104.23, 103.09, 55.72, 21.64, 21.54.
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1 .     cordyol E
C15H16O3     ÏàËÆ¶È:86.6%
Journal of Natural Products          2013          76          547-553
Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus
Min Chen, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     produce 3-O-methyldiorcinol
    ÏàËÆ¶È:85.7%
Planta Medica          2012          78          1861-1866
Cytotoxic Polyphenols from the Fungus Penicillium expansum 091 006 Endogenous with the Mangrove Plant Excoecaria agallocha
Wang, Junfeng; Lu, Zhenyu; Liu, Peipei; Wang, Yi; Li, Jing; Hong, Kui; Zhu, Weiming:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3-hydroxy-5-methylphenyl 2,4-dihydroxy-6-methylbenzoate
C15H14O5     ÏàËÆ¶È:80%
Planta Medica          2012          78          1767-1776
Secondary Metabolites from a Culture of the Fungus Neosartorya pseudofischeri and Their In Vitro Cytostatic Activity in Human Cancer Cells
Eamvijarn, Amnat; Kijjoa, Anake; Bruy¨¨re, C¨¦line; Mathieu, V¨¦ronique; Manoch, Leka; Lefranc, Florence; Silva, Artur; Kiss, Robert; Herz, Werner:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cordyol C
C14H14O4     ÏàËÆ¶È:71.4%
Chemical & Pharmaceutical Bulletin          2007          55(2)          304-307
New Diphenyl Ethers from the Insect Pathogenic Fungus Cordyceps sp.BCC 1861
Taridaporn BUNYAPAIBOONSRI,Seangaroon YOIPROMMARAT, Kamolphan INTEREYA, and Kanokarn KOCHARIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     isohaplopine
C13H11NO4     ÏàËÆ¶È:69.2%
Phytochemistry          1988          27          959-960
Quinoline alkaloids from the leaves of Teclea simplicifolia
Assefa Wondimu,Ermias Dagne,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     2-acetyl-7-methoxybenzofuran
    ÏàËÆ¶È:69.2%
Chemistry of Natural Compounds          2010          46          363-365
A new griseofulvin derivative from the mangrove endophytic fungus Sporothrix SP.
Lu Wen, Zhiyong Guo, Qing Li, Dezhi Zhang and Zhigang She, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     7-Methyl-benzofuran-2-carboxylate
    ÏàËÆ¶È:69.2%
Chemistry of Natural Compounds          2013          49          137-140
Chemical constituents from the mangrove endophytic fungus Sporothrix sp.
Lu Wen, Qiqiu Wei, Gang Chen, Juanni Cai, Zhigang She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     lecanorin
    ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          1396-1399
Effect of Lichen Metabolites on Thylakoid Electron Transport and Photophosphorylation in Isolated Spinach Chloroplasts1
Irma S. Rojas,Blas Lotina-Hennsen, and Rachel Mata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     thamnoliadepside B
C18H18O7     ÏàËÆ¶È:66.6%
Planta Medica          2011          77          2042-2046
Three New Phenolic Compounds from the Lichen Thamnolia vermicularis and Their Antiproliferative Effects in Prostate Cancer Cells
Guo, Jia; Li, Zhan-lin; Wang, Ao-li; Liu, Xiao-qiu; Wang, Jian; Guo, Xin; Jing, Yong-kui; Hua, Hui-ming:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-O-propyldiorcinol
C17H20O3     ÏàËÆ¶È:64.7%
Journal of Natural Products          2013          76          547-553
Bioactive Indole Alkaloids and Phenyl Ether Derivatives from a Marine-Derived Aspergillus sp. Fungus
Min Chen, Chang-Lun Shao, Xiu-Mei Fu, Ru-Fang Xu, Juan-Juan Zheng, Dong-Lin Zhao, Zhi-Gang She, and Chang-Yun Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3,6,7-tri-hydroxy-1-methoxy-xanthone
C14H10O6     ÏàËÆ¶È:64.2%
Natural Product Research          2006          20          1237-1240
Two new xanthones from Hypericum japonicum
P. Fu; W. -D. Zhang; R. H. Liu; T. -Z. Li; Y. -H. Shen; H. -L. Li; W. Zhang; H. -S. Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Gerfelin
C15H14O6     ÏàËÆ¶È:64.2%
Bioscience, Biotechnology, and Biochemistry          2006          70          2523-2528
Synthesis of Gerfelin and Related Analogous Compounds
Md. Sadequl ISLAM, Mitsuhiro KITAGAWA, Masaya IMOTO, Takeshi KITAHARA and Hidenori WATANABE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Tetraorcinol A
C28H26O5     ÏàËÆ¶È:64.2%
Tetrahedron          2011          67          7085-7089
Cyclopeptides and polyketides from coral-associated fungus, Aspergillus versicolor LCJ-5-4
Yibin Zhuang, Xiancun Teng, Yi Wang, Peipei Liu, Hui Wang, Jing Li, Guoqiang Li, Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Orcinoside H
C28H40O14     ÏàËÆ¶È:64.2%
Fitoterapia          2013          86          64-69
Phenolic glycosides from Curculigo orchioides Gaertn.
Zhen-Hui Wang, Jian Huang, Xiao-Ci Ma, Guo-Yu Li, Yue-Ping Ma, Ning Li, Jin-Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     lespeflorin I3
C21H18O6     ÏàËÆ¶È:62.5%
Journal of Natural Products          2009          72          194-203
Melanin Synthesis Inhibitors from Lespedeza floribunda
Maya Mori-Hongo,Hiroyuki Takimoto, Takayuki Katagiri, Makoto Kimura, Yu Ikeda, and Toshio Miyase
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     penicillocitrin A
C16H12O6     ÏàËÆ¶È:62.5%
Natural Product Communications          2013          8          587-588
A New Metabolite from the Endophytic Fungus Penicillium citrinum
Xinlan Li, Liang Zhang, Yanhui Liu, Zhiyong Guo, Zhangshuang Deng, Jianfeng Chen, XuanTu and Kun Zou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     6,8,5',6'-Tetrahydroxy-3'-methylflavone
C16H12O6     ÏàËÆ¶È:62.5%
The Journal of Antibiotics          2013          66          219-223
Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023
Jie Bao, Yu-Lin Sun, Xiao-Yong Zhang, Zhuang Han, Hai-Chun Gao, Fei He, Pei-Yuan Qian and Shu-Hua Qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     6-hydroxymethyleugenin
    ÏàËÆ¶È:61.5%
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   Ì¼Æ×Ä£Äâͼ
19 .     meridianin B
C12H9N4OBr     ÏàËÆ¶È:61.5%
Journal of Natural Products          1998          61          1130-1132
Indole Alkaloids from the Tunicate Aplidium meridianum
Laura Hern¨¢ndez Franco, Elisa Bal de Kier Joff¨¦, Lydia Puricelli, Marcos Tatian, Alicia M. Seldes, and Jorge A. Palermo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     orcinol glucoside
C13H18O7     ÏàËÆ¶È:61.5%
Acta Botanica Yunnanica          2003          25(6)          711-715
A New Lignan Glycoside from Curculigo capitulata
LI Ning,TAN Ning-Hua,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     6H-dibenzo[b,d]pyran-3,9-dihydroxy-6-one
    ÏàËÆ¶È:61.5%
Biochemical Systematics and Ecology          2009          37          535-537
Chemical constituents of Duabanga grandiflora (Lythraceae)
Wanida Auamcharoen, Angsumarn Chandrapatya, Anake Kijjoa, Artur M.S. Silva, Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     orcinol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:61.5%
China Journal of Chinese Materia Medica          2008          33          269-272
Chemical constituents in roots of Hemerocallis fulva
YANG Zhongduo, LI Tao, LI Yuanchao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     anacardoside
    ÏàËÆ¶È:61.5%
Chemical Research in Chinese Universities          199          15          294-299
Synthesis of Analogs of Anacardoside from Semecarpus Anacardium
WANG Yu-lan and CAI Meng-shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Meridianin B
    ÏàËÆ¶È:61.5%
Marine drugs          2010          8          1526-1549
Halogenated Indole Alkaloids from Marine Invertebrates
Patr¨ªcia Mendonça Pauletti,Lucas Silva Cintra,Caio Guedes Braguine,Ademar Alves da Silva Filho,M¨¢rcio Lu¨ªs Andrade e Silva,Wilson Roberto Cunha and Ana Helena Janu¨¢rio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     4-(4-fluoro-1H-indol-3-yl)-2-pyrimidinamine
C12H9FN4     ÏàËÆ¶È:61.5%
Journal of Heterocyclic Chemistry          2007          44          793-801
Dimethylformamide dimethyl acetal in heterocyclic synthesis: Synthesis of polyfunctionally substituted pyridine derivatives as precursors to bicycles and polycycles
Fathi A. Abu-Shanab,A. M. Hessen and S. A. S. Mousa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 8b
C13H12O4     ÏàËÆ¶È:61.5%
Journal of Heterocyclic Chemistry          2000          37          751-755
The birch reduction of heterocyclic compounds V Birch reduction of 2- and 5-acylfuran-3-carboxylic acids and reductive elimination of 2-(arylmethoxymethyl)furan-3-carboxylic acids
Yasuo Ohta, Matsumi Doe, Yoshiki Morimoto and Takamasa Kinoshita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     isobergapten
    ÏàËÆ¶È:61.5%
China Journal of Chinese Materia Medica          2010          35          58-62
Chemical constituents of Incarvillea younghusbandii
FU Yu; BAI Yang; DAWA Zhuoma; BAI Bingru; DING Lisheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3-hydroxy-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one
C13H12O3     ÏàËÆ¶È:61.5%
Heterocycles          2007          71          2721-2733
Al2O3/MeSO3H (AMA) as a Novel Heterogeneous System for Synthesis of Coumarins under Mild Conditions
Hashem Sharghi and Mahboubeh Jokar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 3c
    ÏàËÆ¶È:61.5%
Heterocycles          2004          63          505-508
Dodecasubstituted Porphyrins ¡ª An Easily Accessible Type of Dendritic Porphyrins with Tunable Properties
Claudia Ryppa and Mathias O. Senge*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     7-Hydroxy-3-(3',5'-dihydroxyphenyl)coumarin
C15H10O5     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry Letters          2006          16          257-261
Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin¨Cresveratrol hybrids
Santiago Vilar, El¨ªas Quezada, Lourdes Santana, Eugenio Uriarte, Matilde Y¨¢nez, Nuria Fraiz, Carlos Alcaide, Ernesto Cano, Francisco Orallo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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