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1 . Fumiquinazoline C C24H21N5O4 ÏàËÆ¶È:100% 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 2 . fumiquinazolines C C24H21N5O4 ÏàËÆ¶È:100% 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 3 . Fumiquinazoline C C24H21N5O4 ÏàËÆ¶È:100% 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 4 . fumiquinazoline C C24H21N5O4 ÏàËÆ¶È:91.6% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . fumiquinazoline L C26H25N5O4 ÏàËÆ¶È:80.7% Journal of Natural Products 2013 76 779-782 Structure and Absolute Configuration of Fumiquinazoline L, an Alkaloid from a Gorgonian-Derived Scopulariopsis sp. Fungus Chang-Lun Shao, Ru-Fang Xu, Mei-Yan Wei, Zhi-Gang She, and Chang-Yun Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Fumiquinazoline B C24H23N5O4 ÏàËÆ¶È:75% 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 . compound 12 C24H21N5O3 ÏàËÆ¶È:75% 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 . N-[(1,1,3-Trioxo-2,3-dihydrobenzo[d][1,2]thiazol-2-yl)acetyl]-L-valyl-L-phenylalanine methyl ester C24H26N3O7S ÏàËÆ¶È:66.6% Pharmazie 2002 57 384-392 Synthesis and properties of N-substituted saccharin derivatives L. Soubh - A. Besch - H.-H. Otto Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Hydroxyfumiquinazoline A ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2012 60 3424-3431 Metabolites from Aspergillus fumigatus, an Endophytic Fungus Associated with Melia azedarach, and Their Antifungal, Antifeedant, and Toxic Activities Xiao-Jun Li, Qiang Zhang, An-Ling Zhang, and Jin-Ming Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Fumiquinazoline E ÏàËÆ¶È:64% |

2Â¥2013-07-26 12:37:01
wangwang1989
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xf890529: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-07-26 12:49:32
xf890529: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-07-26 12:49:32
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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£º¹²²éµ½268¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Demethoxyfumitremorgin C C21H23N3O2 ÏàËÆ¶È:100% Tetrahedron 2012 68 4225-4232 Mg(ClO4)2-catalyzed intramolecular allylic amination: application to the total synthesis of demethoxyfumitremorgin C Danfeng Jiang, Zhengren Xu, Yanxing Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . demethoxyfumitremorgin C C21H23N3O2 ÏàËÆ¶È:100% The Journal of Antibiotics 1996 49 534-540 Novel Mammalian Cell Cycle Inhibitors, Tryprostatins A, B and Other Diketopiperazines Produced by Aspergillus fumigatus II. Physico-chemical Properties and Structures CHENG-BIN CUI, HIDEAKI KAKEYA, HIROYUKI OSADA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . demethoxy-fumitremorgin C C21H23N3O2 ÏàËÆ¶È:90.4% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Fumitremorgin C ÏàËÆ¶È:77.2% Natural Product Sciences 2007 13 251-254 12,13-Dihydroxyfumitremorgin C, Fumitremorgin C, and Brevianamide F, Antibacterial Diketopiperazine Alkaloids from the Marine-Derived Fungus Pseudallescheria sp. Zhang, Dahai; Noviendri, Dedi; Nursid, Muhammad; Yang, Xiu-Dong; Son, Byeng-Wha Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . fumitremorgin C ÏàËÆ¶È:77.2% The Journal of Antibiotics 1996 49 534-540 Novel Mammalian Cell Cycle Inhibitors, Tryprostatins A, B and Other Diketopiperazines Produced by Aspergillus fumigatus II. Physico-chemical Properties and Structures CHENG-BIN CUI, HIDEAKI KAKEYA, HIROYUKI OSADA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . fumitremorgin C C22H25N3O3 ÏàËÆ¶È:77.2% Chinese Journal of Antibiotics 2006 31 749-764 º£ÑóÀ´Ô´Õæ¾úA-f -11 ÖÐßÅßá¶þͪßßàºÀ࿹Ö×Áö»îÐԳɷֵÄÑо¿ ÕÔÎÄÓ¢, ÕÅÑÇÅô, ÖìÌì½¾, ·½Óñ´º, Áõºì±ø, ¹ËǫȺ, ÖìΰÃ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cyclotryprostatin C C21H23N3O4 ÏàËÆ¶È:76.1% Tetrahedron 1997 53 59-72 Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase Cheng-Bin Cui, Hideaki Kakeya, Hiroyuki Osada Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . fumitremorgin C C22H25N3O3 ÏàËÆ¶È:72.7% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Fumitremorgin C C22H25N3O3 ÏàËÆ¶È:72.7% Chinese Journal of Applied & Environmental Biology 2010 16 76-78 Isolation and Anti-phytopathogenic Activity of Secondary Metabolites from Alternaria sp. FL25,an Endophytic Fungus in Ficus carica FENG Chengliang & MA Yangmin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . fumitremorgin C 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 |

3Â¥2013-07-26 12:38:21














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