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18.89,24.76,31.54,51.55,58.74,84.29,87.17,87.29,115.62,121.51,124.99,126.35,127.15,128.59,128.77,130.41,135.09,135.86,138.45,146.40,150.44,159.63,170.50,171.00
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18.21,21.93,23.13,25.81,28.59,45.45,51.03,56.94,59.29,106.04,111.39,118.20,119.79,121.91,124.04,126.22,133.82,134.23,136.35,165.85,169.45
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wangwang1989

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
10 .     Fumiquinazoline E
    ÏàËÆ¶È:64%
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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