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1 .     Chaetominine
C22H18N4O4     ÏàËÆ¶È:91.3%
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
2 .     Tryptoquivaline J
C22H18N4O4     ÏàËÆ¶È:78.2%
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
3 .     (-)-chaetominine
    ÏàËÆ¶È:73.9%
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
4 .     Fumiquinazoline E
    ÏàËÆ¶È:68%
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
5 .     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
6 .     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
7 .     N,N'-Bis[methyl(4'-acridinyl)]-p-anisidine
C35H27N3O     ÏàËÆ¶È:60.8%
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
8 .     ethyl-4-(3-(3-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
C24H24N4O4     ÏàËÆ¶È:60.8%
Journal of Heterocyclic Chemistry          2005          42          863-866
Synthesis of novel 4-pyrazolyl-2-oxo-1,2,3,4-tetrahydropyrimidines promoted by phosphotungstic acid
Ganesabaskaran Sivaprasad and Paramasivan T. Peramal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     methyl (2S,3S)-3-hydroxy-2-[(9-phenyl-9-fluorenyl)-amino]-4-pentenoate
C25H23NO3     ÏàËÆ¶È:60.8%
Tetrahedron          2001          57          10071-10076
Efficient synthesis of 3-hydroxyprolines and 3-hydroxyprolinols from sugars
Jin Hwan Lee, Jae Eun Kang, Min Suk Yang, Kyu Young Kang, Ki Hun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound (¡À)-exo-42c
C29H24N4O5S     ÏàËÆ¶È:59.2%
Bioorganic & Medicinal Chemistry          2009          17          94-110
Alantrypinone and its derivatives: Synthesis and antagonist activity toward insect GABA receptors
Takayuki Watanabe, Mitsuhiro Arisawa, Kenji Narusuye, Mohommad Sayed Alam, Kazumi Yamamoto, Masaaki Mitomi, Yoshihisa Ozoe, Atsushi Nishida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Cottoquinazoline D
C24H19N5O4     ÏàËÆ¶È:58.3%
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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