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Neoechinulin A
C19H21N3O2     ÏàËÆ¶È:100%
Natural Product Research and Development          2012          24          427-431
Chemical Constituents from Inula hupehensis
ZHANG Fei; QIN Jiang-jiang; CHENG Xiang-rong; JIN Hui-zi; ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     brevianamide S
C42H40N6O4     ÏàËÆ¶È:71.4%
Organic Letters          2012          14          4770-4773
Brevianamides with Antitubercular Potential from a Marine-Derived Isolate of Aspergillus versicolor
Fuhang Song, Xinru Liu, Hui Guo, Biao Ren, Caixia Chen, Andrew M. Piggott, Ke Yu, Hong Gao, Qian Wang, Mei Liu, Xueting Liu, Huanqin Dai, Lixin Zhang, and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     brevianamide U
C21H23N3O4     ÏàËÆ¶È:71.4%
Organic Letters          2012          14          4770-4773
Brevianamides with Antitubercular Potential from a Marine-Derived Isolate of Aspergillus versicolor
Fuhang Song, Xinru Liu, Hui Guo, Biao Ren, Caixia Chen, Andrew M. Piggott, Ke Yu, Hong Gao, Qian Wang, Mei Liu, Xueting Liu, Huanqin Dai, Lixin Zhang, and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     neoechinulin A
    ÏàËÆ¶È:68.4%
Bioscience, Biotechnology, and Biochemistry          1999          63          932-933
Isolation of an Antioxidative Substance Produced by Aspergillus repens
Ryuta YAGI, Mikiharu DOI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     8,9-dihydrobarettin
C17H22N6O2Br     ÏàËÆ¶È:63.1%
Journal of Natural Products          2004          67          368-372
Antifouling Activity of Brominated Cyclopeptides from the Marine Sponge Geodia barretti
Martin Sjgren, Ulf Gransson, Ann-Louise Johnson, Mia Dahlstrm,Rolf Andersson, Jan Bergman, Per R. Jonsson, and Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     cristatumin A
C19H21N3O3     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry Letters          2012          22          4650-4653
Cristatumins A¨CD, new indole alkaloids from the marine-derived endophytic fungus Eurotium cristatum EN-220
Feng-Yu Du, Xiao-Ming Li, Chun-Shun Li, Zhuo Shang, Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     Brevianamide J
C42H42N6O5     ÏàËÆ¶È:60%
Organic Letters          2009          Vol.11,No.16          3714-3717
Brevianamide J, A New Indole Alkaloid Dimer from Fungus Aspergillus versicolor
Guo-You Li, Tao Yang, Ying-Gang Luo, Xiao-Zhen Chen, Dong-Mei Fang, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     acetylmollugin
    ÏàËÆ¶È:57.8%
Chemical & Pharmaceutical Bulletin          1983          31          2353-2358
Studies on a Novel Anthraquinone and Its Glycosides isolated from Rubia cordifolia and R. akane
HIDEJI ITOKAWA,KAZUHIKO MIHARA and KOICHI TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     Aristolochic acid III
    ÏàËÆ¶È:57.8%
Journal of Natural Products          1992          Vol 55          918
9-Methoxy- and 7,9-Dimethoxytariacuripyrone, Natural Nitro-Compounds with a New Basic Skeleton from Aristolochia brevipes
Hans Achenbach, Reiner Waibel, Manfred Zwanzger, Xorge A. Dominguez, Griselda Espinosa B., Julia Verde S., Humberto S¨¢nchez V.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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--------------------------------------------------------------------------------

1 .     Neoechinulin A
C19H21N3O2     ÏàËÆ¶È:100%
Natural Product Research and Development          2012          24          427-431
Chemical Constituents from Inula hupehensis
ZHANG Fei; QIN Jiang-jiang; CHENG Xiang-rong; JIN Hui-zi; ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     brevianamide S
C42H40N6O4     ÏàËÆ¶È:71.4%
Organic Letters          2012          14          4770-4773
Brevianamides with Antitubercular Potential from a Marine-Derived Isolate of Aspergillus versicolor
Fuhang Song, Xinru Liu, Hui Guo, Biao Ren, Caixia Chen, Andrew M. Piggott, Ke Yu, Hong Gao, Qian Wang, Mei Liu, Xueting Liu, Huanqin Dai, Lixin Zhang, and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     brevianamide U
C21H23N3O4     ÏàËÆ¶È:71.4%
Organic Letters          2012          14          4770-4773
Brevianamides with Antitubercular Potential from a Marine-Derived Isolate of Aspergillus versicolor
Fuhang Song, Xinru Liu, Hui Guo, Biao Ren, Caixia Chen, Andrew M. Piggott, Ke Yu, Hong Gao, Qian Wang, Mei Liu, Xueting Liu, Huanqin Dai, Lixin Zhang, and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     neoechinulin A
    ÏàËÆ¶È:68.4%
Bioscience, Biotechnology, and Biochemistry          1999          63          932-933
Isolation of an Antioxidative Substance Produced by Aspergillus repens
Ryuta YAGI, Mikiharu DOI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     8,9-dihydrobarettin
C17H22N6O2Br     ÏàËÆ¶È:63.1%
Journal of Natural Products          2004          67          368-372
Antifouling Activity of Brominated Cyclopeptides from the Marine Sponge Geodia barretti
Martin Sjgren, Ulf Gransson, Ann-Louise Johnson, Mia Dahlstrm,Rolf Andersson, Jan Bergman, Per R. Jonsson, and Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     cristatumin A
C19H21N3O3     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry Letters          2012          22          4650-4653
Cristatumins A¨CD, new indole alkaloids from the marine-derived endophytic fungus Eurotium cristatum EN-220
Feng-Yu Du, Xiao-Ming Li, Chun-Shun Li, Zhuo Shang, Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     Brevianamide J
C42H42N6O5     ÏàËÆ¶È:60%
Organic Letters          2009          Vol.11,No.16          3714-3717
Brevianamide J, A New Indole Alkaloid Dimer from Fungus Aspergillus versicolor
Guo-You Li, Tao Yang, Ying-Gang Luo, Xiao-Zhen Chen, Dong-Mei Fang, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     acetylmollugin
    ÏàËÆ¶È:57.8%
Chemical & Pharmaceutical Bulletin          1983          31          2353-2358
Studies on a Novel Anthraquinone and Its Glycosides isolated from Rubia cordifolia and R. akane
HIDEJI ITOKAWA,KAZUHIKO MIHARA and KOICHI TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     Aristolochic acid III
    ÏàËÆ¶È:57.8%
Journal of Natural Products          1992          Vol 55          918
9-Methoxy- and 7,9-Dimethoxytariacuripyrone, Natural Nitro-Compounds with a New Basic Skeleton from Aristolochia brevipes
Hans Achenbach, Reiner Waibel, Manfred Zwanzger, Xorge A. Dominguez, Griselda Espinosa B., Julia Verde S., Humberto S¨¢nchez V.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     (2-Phenyl-1-thioxo-1,2,3,4-tetrahydro-¦Â-carbolin-9-yl)-acetic acid t-butyl ester
C23H24O2N2S     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2012          20          356-367
Design, synthesis, and biological evaluation of novel (1-thioxo-1,2,3,4-tetrahydro-b-carbolin-9-yl)acetic acids as selective inhibitors for AKR1B1
Daisuke Minehira, Daisuke Takeda, Hirokazu Urata, Atsushi Kato, Isao Adachi, Xu Wang,Yuji Matsuya, Kenji Sugimoto, Mayuko Takemura, Satoshi Endo, Toshiyuki Matsunaga,Akira Hara, Jun Koseki, Kayo Narukawa, Shuichi Hirono, Naoki Toyooka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     methyl1,6-dihydro-5-methylpyrrolo[4',5':5,6]pyrido[3,4-b]indole-2-carboxylate
C16H13N3O2     ÏàËÆ¶È:57.8%
Journal of Heterocyclic Chemistry          2004          41          531-540
Synthesis of some fused ¦Â-carbolines including the first example of the pyrrolo[3,2-c]-¦Â-carboline system
Glenn C. Condie and Jan Bergman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     6-acetoxy-1-(2-oxo-2-phenylethyl)quinolin-2(1H)-one
C19H15NO4     ÏàËÆ¶È:57.8%
Heterocycles          2003          60          131-141
Synthesis of Dibenzo[a,f]quinolizinium and 2-Phenyloxazolo[3,2-a]quinolinium Perchlorates via Acid-catalyzed Cyclization of 1-(2-Oxo-2-phenylethyl)quinoline-2(1H)-ones
I-Li Chen, Yeh-Long Chen, Tai-Chi Wang, and Cherng-Chyi Tzeng*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     6-acetoxy-1-(2-oxo-2-p-tolylethyl)quinolin-2(1H)-one
C20H17NO4     ÏàËÆ¶È:57.8%
Heterocycles          2003          60          131-141
Synthesis of Dibenzo[a,f]quinolizinium and 2-Phenyloxazolo[3,2-a]quinolinium Perchlorates via Acid-catalyzed Cyclization of 1-(2-Oxo-2-phenylethyl)quinoline-2(1H)-ones
I-Li Chen, Yeh-Long Chen, Tai-Chi Wang, and Cherng-Chyi Tzeng*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     2-(1-Propionylaminoethyl)thiazole-4-carboxylic acid [2-(1H-indol-3-yl)-ethyl]amide
C19H22N4O2S     ÏàËÆ¶È:57.8%
Magnetic Resonance in Chemistry          2008          46          80-83
Tryptamine derived amides with thiazole ring system from Thermoactinomyces strain TA66-2 (pages 80¨C83)
aǧla Akmemiş Korkmaz, E. Esin Hameş-Kocabaş, Ataç Uzel and Erdal Bedir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     2-(1-acetylaminoethyl)thiazole-4-carboxylic acid [2-(1H-indol-3-yl)ethyl]amide
C18H20N4O2S     ÏàËÆ¶È:57.8%
Magnetic Resonance in Chemistry          2008          46          80-83
Tryptamine derived amides with thiazole ring system from Thermoactinomyces strain TA66-2 (pages 80¨C83)
aǧla Akmemiş Korkmaz, E. Esin Hameş-Kocabaş, Ataç Uzel and Erdal Bedir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     compound
    ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          1998          6          1309-1335
Synthesis and activity of bivalent FKBP12 ligands for the regulated dimerization of proteins
Terence Keenan, David R. Yaeger, Nancy L. Courage, Carl T. Rollins, Mary Ellen Pavone, Victor M. Rivera, Wu Yang, Tao Guo, Jane F. Amara, Tim Clackson, Michael Gilman, Dennis A. Holt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     2,2'-dicarboxy-5,5',6,6'-tetrahydroxy-3,4'-biindolyl
C18H13N2O8     ÏàËÆ¶È:57.8%
Tetrahedron          1996          52          7913-7920
Oxidative polymerisation of 5,6-dihydroxyindole-2-carboxylic acid to melanin: A new insight
Alessandro Pezzella, Alessandra Napolitano, Marco d'Ischia, Giuseppe Prota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     2-(1H-indol-3-yl)-6-methylquinoline-3-carbonitrile
C19H13N3     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2012          20          2199-2207
C¨CC bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors
K. Shiva Kumar, S. Kiran Kumar, B. Yogi Sreenivas, Dhilli Rao Gorja, Ravikumar Kapavarapu, D. Rambabu, G. Rama Krishna, C. Malla Reddy, M.V. Basaveswara Rao, Kishore V.L. Parsa, Manojit Pal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     (E)-N'-[1-(1H-indol-2-yl)ethylidene]-5-bromo-2-ethoxybenzohydrazide
C19H18BrN3O     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2012          20          7069-7082
Optimization and structure¨Cactivity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents
Nag S. Kumar, Emily A. Amandoron, Artem Cherkasov, B. Brett Finlay, Huansheng Gong, Linda Jackson, Sukhbir Kaur, Tian Lian, Anne Moreau, Christophe Labri¨¨re, Neil E. Reiner, Raymond H. See, Natalie C. Strynadka, Lisa Thorson, Edwin W.Y. Wong, Liam Worrall
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     Methyl {2-[(2-1H-indazol-3-yl)ethyl]-3-oxo-2,3-dihydro-1H-isoindol-1-yl}acetate
C21H20N2O3     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2005          83          990-1005
Synthesis of N-substituted isoindolinones via a palladium catalysed three-component carbonylation - amination - Michael addition cascade1
Ronald Grigg, Xinjie Gai, Tossapol Khamnaen, Shuleewan Rajviroongit,Visuvanathar Sridharan, Lixin Zhang, Simon Collard, and Ann Keep
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-05-08 20:11:05
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