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1 .     Chaetominine
C22H18N4O4     ÏàËÆ¶È:86.3%
Organic Letters          2006          8          5709-5712
Chaetominine, a Cytotoxic Alkaloid Produced by Endophytic Chaetomium sp. IFB-E015
Rui H. Jiao, Shu Xu,Jun Y. Liu, Hui M. Ge, Hui Ding, Chen Xu, Hai L. Zhu, and Ren X. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (-)-chaetominine
    ÏàËÆ¶È:72.7%
Chinese Pharmaceutical Journal          2011          46          1154-1158
Metabolites of Aspergillus sp. HT-2
ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Tryptoquivaline J
C22H18N4O4     ÏàËÆ¶È:68.1%
Chemistry of Natural Compounds          2005          41          236-238
ALKALOIDS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus
Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     norquinadoline A
C26H25N5O4     ÏàËÆ¶È:65.3%
Journal of Natural Products          2013          76          1133-1140
Antiviral Alkaloids Produced by the Mangrove-Derived Fungus Cladosporium sp. PJX-41
Jixing Peng, Tao Lin, Wei Wang, Zhihong Xin, Tianjiao Zhu, Qianqun Gu, and Dehai Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     lapatin A
C23H19O3N5     ÏàËÆ¶È:65.2%
Journal of Natural Products          2005          68          871-874
Discovery of New Natural Products by Application of X-hitting, a Novel Algorithm for Automated Comparison of Full UV Spectra,Combined with Structural Determination by NMR Spectroscopy
Thomas Ostenfeld Larsen, Bent O. Petersen, Jens . Duus,Dan Srensen, Jens C. Frisvad, and Michael E. Hansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Tryptoquivaline Q
C23H22N4O5     ÏàËÆ¶È:65.2%
Journal of Asian Natural Products Research          2012          14          1109-1115
Two new alkaloids from a marine-derived fungus Neosartorya sp.HN-M-3
Feng-Yuan Sun, Gang Chen, Jiao Bai, Wen Li & Yue-Hu Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Fumiquinazoline E
    ÏàËÆ¶È:64%
Journal of the Chemical Society, Perkin Transactions 1          1995                   2345-2353
Fumiquinazolines A¨CG, novel metabolites of a fungus separated from a Pseudolabrus marine fish
Chika Takahashi, Tomochika Matsushita, Mitsunobu Doi, Katsuhiko Minoura, Tetsuro Shingu, Yuko Kumeda and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (E)-ethyl-1-phenylsulfonyl-3-(2-(acetamidomethyl)-1H-indol-3-yl)acrylate
C22H22N2O5S     ÏàËÆ¶È:63.6%
Indian Journal of Chemistry          2010          49B          327-334
Lewis-acid mediated acetamidation of N-pro­tected bromomethylindoles
Vasudevan Dhayalan & Arasambattu K Mohanakrishnan*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     tryptoquivaline H
C22H18N4O5     ÏàËÆ¶È:63.6%
Tetrahedron          2012          68          3253-3262
Sartorymensin, a new indole alkaloid, and new analogues of tryptoquivaline and fiscalins produced by Neosartorya siamensis (KUFC 6349)
Suradet Buttacho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     fumiquinazolines A
C24H23N5O4     ÏàËÆ¶È:62.5%
China Journal of Chinese Materia Medica          2007          32          1848-1851
Study on Indole-Quinazolines Alkaloids from Marine-Derived Fungus Aspergillus sydowi PFW-13 and their Anti-Tumor Activities
ZHANG Min, FANG Yuchun, ZHU Tianjiao, ZHAO Wenying, GU Qianqun, HAN Xiaoxian, ZHU Weiming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Cottoquinazoline D
C24H19N5O4     ÏàËÆ¶È:62.5%
Organic Letters          2011          Vol.13,No.5          1130-1133
New Quinazolinone Alkaloids within Rare Amino Acid Residue from Coral-Associated Fungus, Aspergillus versicolor LCJ-5-4
Yibin Zhuang, Xiancun Teng, Yi Wang, Peipei Liu, Guoqiang Li, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     Fumiquinazoline A
C24H23N5O4     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1995                   2345-2353
Fumiquinazolines A¨CG, novel metabolites of a fungus separated from a Pseudolabrus marine fish
Chika Takahashi, Tomochika Matsushita, Mitsunobu Doi, Katsuhiko Minoura, Tetsuro Shingu, Yuko Kumeda and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Fumiquinazoline D
C24H21N5O4     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1995                   2345-2353
Fumiquinazolines A¨CG, novel metabolites of a fungus separated from a Pseudolabrus marine fish
Chika Takahashi, Tomochika Matsushita, Mitsunobu Doi, Katsuhiko Minoura, Tetsuro Shingu, Yuko Kumeda and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 12
C24H21N5O3     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1995                   2345-2353
Fumiquinazolines A¨CG, novel metabolites of a fungus separated from a Pseudolabrus marine fish
Chika Takahashi, Tomochika Matsushita, Mitsunobu Doi, Katsuhiko Minoura, Tetsuro Shingu, Yuko Kumeda and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     fiscalin A
C26H27N5O4     ÏàËÆ¶È:61.5%
Tetrahedron          2012          68          3253-3262
Sartorymensin, a new indole alkaloid, and new analogues of tryptoquivaline and fiscalins produced by Neosartorya siamensis (KUFC 6349)
Suradet Buttacho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Cottoquinazoline B
C23H19N5O4     ÏàËÆ¶È:60.8%
Organic Letters          2011          Vol.13,No.5          1130-1133
New Quinazolinone Alkaloids within Rare Amino Acid Residue from Coral-Associated Fungus, Aspergillus versicolor LCJ-5-4
Yibin Zhuang, Xiancun Teng, Yi Wang, Peipei Liu, Guoqiang Li, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     tryptoquivaline l
C23H20N4O5     ÏàËÆ¶È:60.8%
Tetrahedron          2012          68          3253-3262
Sartorymensin, a new indole alkaloid, and new analogues of tryptoquivaline and fiscalins produced by Neosartorya siamensis (KUFC 6349)
Suradet Buttacho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     ethyl 2-(benzylthio)-4-hydroxybenzo[h]quinoline-3-carboxylate
C23H19NO3S     ÏàËÆ¶È:60.8%
Heterocycles          2012          85          103-122
Polycyclic Quinolones (Part 1) ¡ª Thieno[2,3-b]benzo[h]quinoline Derivatives: Design, Synthesis, Preliminary in vitro and in silico Studies
Abeer Ahmed and Mohsen Daneshtalab
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     quinadoline A
    ÏàËÆ¶È:59.2%
Journal of Natural Products          2013          76          1133-1140
Antiviral Alkaloids Produced by the Mangrove-Derived Fungus Cladosporium sp. PJX-41
Jixing Peng, Tao Lin, Wei Wang, Zhihong Xin, Tianjiao Zhu, Qianqun Gu, and Dehai Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     N,N'-Bis[methyl(4'-acridinyl)]-p-anisidine
C35H27N3O     ÏàËÆ¶È:59.0%
Molecules          2001          6          673-682
Synthesis of new Bis- and Tetra-Acridines
Val¨¦rie Sourdon, St¨¦phane Mazoyer, Val¨¦rie Pique and Jean-Pierre Galy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-08-23 08:27:45
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