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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½298¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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