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2Â¥2013-08-23 08:27:31
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
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- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
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xf890529: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÁ˰¡ 2013-08-26 08:32:10
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²éѯ½á¹û£º¹²²éµ½414¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
3Â¥2013-08-23 08:27:45














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