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18.11,22.20,25.49,25.98,28.90,45.05,48.65,49.25,58.40,68.08,83.20,106.03,111.27,118.59,120.18,120.84,124.20,126.36,131.51,133.10,136.66,170.52
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18.35,22.46,25.78,29.22,45.42,49.63,55.52,58.74,68.25,83.49,95.03,106.22,108.89,120.89,124.55,130.28,133.41,137.79,155.59,166.45,171.02
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1 .     cyclotryprostatin C
C21H23N3O4     ÏàËÆ¶È:90.9%
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
2 .     12,13-dihydroxyfumitremorgin C
C22H25N3O5     ÏàËÆ¶È:81.8%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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 .     10,11-dihydroxy-fumitremorgin C
C23H21N5O4     ÏàËÆ¶È:81.8%
Phytochemistry          1990          29          1025-1026
12,13-Dihydroxy-fumitremorgin C from Aspergillus fumigatus
Wolf-Rainer Abraham,Hans-Adolf Arfmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     demethoxy-fumitremorgin C
C21H23N3O2     ÏàËÆ¶È:81.8%
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 .     Demethoxyfumitremorgin C
C21H23N3O2     ÏàËÆ¶È:81.8%
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
6 .     demethoxyfumitremorgin C
C21H23N3O2     ÏàËÆ¶È:81.8%
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
7 .     19S-hydroxy-16-epi-tacamine
C21H26N2O4     ÏàËÆ¶È:77.2%
Acta Botanica Yunnanica          1999          21(3)          399-405
The Constituents of Ervatamia yunnanensis
YU Yang,GAO Jin-Ming,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     12R,13S-Dihydroxyfumitremorgin 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
9 .     (-)-16R,21R-O-methyleburnamine
C20H26N2O     ÏàËÆ¶È:77.2%
Phytochemistry          1991          30          1285-1293
Alkaloids from Rhazya stricta
Atta-ur-Rahman, Khurshid Zaman, Shahnaz Perveen, Habib-ur-Rehman, Anium Muzaffar, M.Iqbal Choudhary, Azra Pervin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     dihydroxy-fumitremorgin C
C22H25N3O5     ÏàËÆ¶È:77.2%
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
11 .     epi-Demethoxyfumitremorgin C
C21H23N3O2     ÏàËÆ¶È:77.2%
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
12 .     demethoxyfumitremorgin C
C21H23N3O2     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
13 .     fumitremorgin B
C27H33O5     ÏàËÆ¶È:74.0%
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
14 .     fumitremorgin B
C27H33N3O5     ÏàËÆ¶È:74.0%
Chemistry of Natural Compounds          2013          49          568-570
Isolation and biological evaluation of secondary metabolites of the endophytic fungus Aspergillus fumigatus from Astragalus membranaceus
Feng Zhou, Hongchi Zhang, Rui Liu, Dongxu Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Fumitremorgin B
C27H33N3O5     ÏàËÆ¶È:74.0%
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
16 .     NA-209B
C27H33N3O5     ÏàËÆ¶È:74.0%
Chinese Journal of Antibiotics          2000          25          257-271
΢ÉúÎïÀ´Ô´µÄµ¨¹Ì´¼õ£»ù×ªÒÆÃ¸ÒÖÖÆ¼ÁÑо¿¢ò. NA-209A, B µÄÀí»¯ÌØÕ÷ºÍ½á¹¹¼ø±ð
ÌÆÓÂ, Ñî´ó¾ü, Ò¦Ìì¾ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 3
    ÏàËÆ¶È:73.9%
Organic Magnetic Resonance          1976          8          618-622
Benzo- and indoloquinolizines: X¡ªapplication of carbon-13 n.m.r. to the stereochemistry of the 4b, 5, 6, 7, 8, 8a, 10, 11, 16, 16b-decahydrodibenz[f, h]indolo[2, 3-a]quinolizine isomers
G. Van Binst, D. Tourw¨¦ and E. De Cock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Fumitremorgin C
C22H25N3O3     ÏàËÆ¶È:72.7%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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
19 .     Fumitremorgin C
    ÏàËÆ¶È:72.7%
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
20 .     9-Hydroxyfumitremorgin C
C22H25N3O4     ÏàËÆ¶È:72.7%
Chemistry & Biodiversity          2012          9          385-393
2,5-Diketopiperazines from the Marine-Derived Fungus Aspergillus fumigatus YK-7
Yu Wang, Zhan-Lin Li, Jiao Bai, Li-Min Zhang, Xin Wu, Lin Zhang,Yue-Hu Pei, Yong-Kui Jing, and Hui-Ming Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     2-(2-tri-n-butylstannyl-(Z)-but-2-en-1-yl)-1,2,3,4,5,7-hexahydro-6H-6-methylazocino[4,3-b]indol-6-ol
C26H41N2O120Sn     ÏàËÆ¶È:72.7%
Heterocycles          2010          82          349-370
Synthesis of 1,2,3,4,5,7-Hexahydro-6H-azocino[4,3-b]indol-6-ones as Intermediates for the Synthesis of Apparicine
Jason G. Kettle, David Roberts, and John A. Joule
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     14,15-dihydro-14-hydroxymethylebunamenin-14-ol
C20H26N2O2     ÏàËÆ¶È:72.7%
Heterocycles          2007          71          2347-2362
Synthesis of 18-Hydroxyvincamines and Epoxy-1, 14-secovincamines; A New Proof for the Aspidospermane-Eburnane Rearrangement
Andr¨¢s Nemes, Csaba Sz¨¢ntay Jr., L¨¢szl¨® Czibula, and Istv¨¢n Greiner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     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
24 .     compound 26
    ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          1998          6          1233-1241
Biomimetic diels¨Calder cyclizations for the construction of the brevianamide, paraherquamide, sclerotamide, asperparaline and VM55599 ring systems
Robert M Williams, Juan F Sanz-Cervera, F¨¦lix Sancen¨®n, J.Alberto Marco, Kathleen M Halligan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 8
C21H25N3O2     ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          2008          16          4626-4651
Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     2-isoprenyl-3-(6-isothiocyanato-1H-indol-3-ylmethyl)-hexahydro-pyrrolo[1,2-a]pyrazine-1,4-dione
C22H24N4O2     ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          2008          16          4626-4651
Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     fumitremorgin C
    ÏàËÆ¶È:72.7%
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
28 .     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
29 .     tryprostatin B
C21H25N3O2     ÏàËÆ¶È:72.7%
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
30 .     fumitremorgin B
    ÏàËÆ¶È:70.3%
Chemical & Pharmaceutical Bulletin          1980          28          245-254
Chemistry of Tremorogenic Metabolites. I. Fumitremorgin A from Aspergillus fumigatus
MIKIO YAMAZAKI,HARUHIRO FUJIMOTO and TAKAO KAWASAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     Fumitremorgin B
C27H33N3O5     ÏàËÆ¶È:70.3%
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
32 .     verruculogen
    ÏàËÆ¶È:70.3%
Natural Product Research and Development          2013          25          64-67
Studies on Secondary Metabolites Produced by Endophytic Aspergillus fumigatus from Trifolium repens
YANG Yong-xun, DONG Xiao-ping, YAN Yong-ming, TAO Ming, LUO Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     verruculogen
C27H33N3O7     ÏàËÆ¶È:70.3%
Chemistry of Natural Compounds          2013          49          568-570
Isolation and biological evaluation of secondary metabolites of the endophytic fungus Aspergillus fumigatus from Astragalus membranaceus
Feng Zhou, Hongchi Zhang, Rui Liu, Dongxu Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     NA-209A
C27H33N3O7     ÏàËÆ¶È:70.3%
Chinese Journal of Antibiotics          2000          25          257-271
΢ÉúÎïÀ´Ô´µÄµ¨¹Ì´¼õ£»ù×ªÒÆÃ¸ÒÖÖÆ¼ÁÑо¿¢ò. NA-209A, B µÄÀí»¯ÌØÕ÷ºÍ½á¹¹¼ø±ð
ÌÆÓÂ, Ñî´ó¾ü, Ò¦Ìì¾ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     fumitremorgin B
C27H33N3O5     ÏàËÆ¶È:70.3%
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
36 .     Intermediate
C26H31N3O4     ÏàËÆ¶È:69.5%
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
37 .     compound 1b
C23H31N3O2     ÏàËÆ¶È:69.5%
The Journal of Antibiotics          2011          64          679-681
A new cytotoxic indole-3-ethenamide from the halotolerant fungus Aspergillus sclerotiorum PT06-1
Hui Wang, Jin-Kai Zheng, Hai-Jun Qu, Pei-Pei Liu, Yi Wang and Wei-Ming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 1
    ÏàËÆ¶È:69.5%
Organic Magnetic Resonance          1976          8          618-622
Benzo- and indoloquinolizines: X¡ªapplication of carbon-13 n.m.r. to the stereochemistry of the 4b, 5, 6, 7, 8, 8a, 10, 11, 16, 16b-decahydrodibenz[f, h]indolo[2, 3-a]quinolizine isomers
G. Van Binst, D. Tourw¨¦ and E. De Cock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     (1Z,3E,7E,11E)-14-acetoxycembra-1,3,7,11-tetraene-9,10-diol
C22H34O4     ÏàËÆ¶È:68.1%
Journal of Natural Products          2003          66          1284-1287
New Cembrane Diterpenes of the Marine Octocoral Eunicea tourniforti from the Eastern Caribbean
Kelly I. Marville,Stewart McLean, William F. Reynolds,and Winston F. Tinto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     corynanthine
C21H25N2O3     ÏàËÆ¶È:68.1%
Planta Medica          2000          66          531-536
Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras
Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
»¯ºÏÎï2£º
²éѯ½á¹û£º¹²²éµ½4252¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     12,13-dihydroxyfumitremorgin C
C22H25N3O5     ÏàËÆ¶È:95.4%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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 .     12R,13S-Dihydroxyfumitremorgin C
    ÏàËÆ¶È:95.4%
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
3 .     10,11-dihydroxy-fumitremorgin C
C23H21N5O4     ÏàËÆ¶È:95.4%
Phytochemistry          1990          29          1025-1026
12,13-Dihydroxy-fumitremorgin C from Aspergillus fumigatus
Wolf-Rainer Abraham,Hans-Adolf Arfmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     dihydroxy-fumitremorgin C
C22H25N3O5     ÏàËÆ¶È:90.9%
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 .     Fumitremorgin C
C22H25N3O3     ÏàËÆ¶È:86.3%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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
6 .     Fumitremorgin C
    ÏàËÆ¶È:86.3%
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
7 .     fumitremorgin C
C22H25N3O3     ÏàËÆ¶È:86.3%
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
8 .     fumitremorgin C
    ÏàËÆ¶È:86.3%
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
9 .     Fumitremorgin C
C22H25N3O3     ÏàËÆ¶È:86.3%
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
C22H25N3O3     ÏàËÆ¶È:86.3%
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
11 .     cyclotryprostatin A
C22H25N3O5     ÏàËÆ¶È:81.8%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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
12 .     9-Hydroxyfumitremorgin C
C22H25N3O4     ÏàËÆ¶È:81.8%
Chemistry & Biodiversity          2012          9          385-393
2,5-Diketopiperazines from the Marine-Derived Fungus Aspergillus fumigatus YK-7
Yu Wang, Zhan-Lin Li, Jiao Bai, Li-Min Zhang, Xin Wu, Lin Zhang,Yue-Hu Pei, Yong-Kui Jing, and Hui-Ming Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     cyclotryprostatin A
C22H25N3O5     ÏàËÆ¶È:81.8%
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
14 .     Cyclotryprostatin A
    ÏàËÆ¶È:81.8%
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
15 .     fumitremorgin C
    ÏàËÆ¶È:81.8%
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
16 .     cyclotryprostatin C
C21H23N3O4     ÏàËÆ¶È:80.9%
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
17 .     cyclotryprostatin B
C23H27N3O5     ÏàËÆ¶È:78.2%
Chemistry of Natural Compounds          2004          40          615-617
FUMITREMORGINS 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
18 .     cyclotryprostatin B
C23H27N3O5     ÏàËÆ¶È:78.2%
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
19 .     cyclotryprostatin B
C23H27N3O5     ÏàËÆ¶È:78.2%
Chemistry of Natural Compounds          2013          49          568-570
Isolation and biological evaluation of secondary metabolites of the endophytic fungus Aspergillus fumigatus from Astragalus membranaceus
Feng Zhou, Hongchi Zhang, Rui Liu, Dongxu Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     rel-(8R)-9-hydroxy-8-methoxy-18-epi-fumitremorgin C
C23H27N3O5     ÏàËÆ¶È:78.2%
Helvetica Chimica Acta          2012          95          1401-1408
Diketopiperazine Alkaloids Produced by the Endophytic Fungus Aspergillus fumigatus from the Stem of Erythrophloeum fordiiOliv.
Yu-Xi Liu, Shuang-Gang Ma, Xiao-Jing Wang, Nan Zhao, Jing Qu, Shi-Shan Yu, Jun-Gui Dai, Ying-Hong Wang and Yi-Kang Si
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     cyclotryprostatins B
C23H27N3O5     ÏàËÆ¶È:78.2%
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
22 .     cyclotryprostatin B
    ÏàËÆ¶È:78.2%
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
23 .     verruculogen TR-2
C22H27N3O6     ÏàËÆ¶È:77.2%
Natural Product Research          2013          27          967-974
Time course production of indole alkaloids by an endophytic strain of Penicillium brasilianum cultivated in rice
Taicia Pacheco Fill, Helo¨ªsa Briganti Rodrigues Asenha, Anna Silvia Marques, Antônio Gilberto Ferreira & Edson Rodrigues-Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     demethoxy-fumitremorgin C
C21H23N3O2     ÏàËÆ¶È:76.1%
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
25 .     tryprostation A
C22H27N3O3     ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          2008          16          4626-4651
Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     2-benzyl-3-(6-methoxy-1H-indol-3-ylmethyl)-hexahydro-pyrrolo[1,2-a]pyrazine-1,4-dione
C24H25N3O3     ÏàËÆ¶È:72.7%
Bioorganic & Medicinal Chemistry          2008          16          4626-4651
Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     tryprostatin A
C22H27N3O3     ÏàËÆ¶È:72.7%
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
28 .     Demethoxyfumitremorgin C
C21H23N3O2     ÏàËÆ¶È:71.4%
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
29 .     2-isoprenyl-3-(6-amino-1H-indol-3-ylmethyl)-hexahydro-pyrrolo[1,2-a]pyrazine-1,4-dione
C21H26N4O2     ÏàËÆ¶È:71.4%
Bioorganic & Medicinal Chemistry          2008          16          4626-4651
Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     demethoxyfumitremorgin C
C21H23N3O2     ÏàËÆ¶È:71.4%
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
31 .     Dodoviscin J
C22H22O7     ÏàËÆ¶È:68.1%
Journal of Natural Products          2012          75          699-706
Isoprenylated Flavonoid and Adipogenesis-Promoting Constituents of Dodonaea viscosa
Lai-Bin Zhang, Jun Ji, Chun Lei, He-Yao Wang, Qin-Shi Zhao, and Ai-Jun Hou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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