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xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-03 09:26:46
²éѯ½á¹û£º¹²²éµ½1429¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Nb-acetyltryptamine
C12H14N2O     ÏàËÆ¶È:85.7%
Archives of Pharmacal Research          2003          26          21-23
Indolyl alkaloid derivatives,Nb-acetyltryptamine and oxaline from a marine-derived fungus
Yong Li, Xi Feng Li, Dong Soo Kim, Hong Dae Choi and Byeng Wha Son
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     N-acetyl-tryptamine
C12H14N2O     ÏàËÆ¶È:78.5%
Chemistry of Natural Compounds          2006          42          713-717
INDOLIC METABOLITES FROM THE NEW MARINE BACTERIUM Roseivirga echinicomitans KMM 6058T
G. K. Oleinikova,O. I. Ivchuk, V. A. Denisenko, E. L. Chaikina,N. I. Menzorova, O. I. Nedashkovskaya, and T. A. Kuznetsova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Nb-ÒÒõ£É«°·
    ÏàËÆ¶È:78.5%
Chinese Journal of Antibiotics          2012          37          366-371
Purification and characterization of anti multi¡¤drug-resistant bacterial constituents from fermentation broth of Actinoplanes sp.PDF-1
Li Zi-qiang, Wang Li-ning, Hu Xin-xin, Wei Yu-zhen, Liu Hong, yu, Zhang Yu-qin, Wang Yu-cheng, You Xue-fu and Yu Li-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 13a
C14H16N2O3     ÏàËÆ¶È:71.4%
Journal of Natural Products          2005          68          1581-1587
Extraction, Hemisynthesis, and Synthesis of Canthin-6-one Analogues. Evaluation of Their Antifungal Activities
Flor Soriano-Agatn, Delphine Lagoutte, Erwan Poupon, Franois Roblot,Alain Fournet, Jean-Charles Gantier, and Reynald Hocquemiller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-(1-Nitromethylpentyl)-1H-indole
C14H18O2N2     ÏàËÆ¶È:71.4%
Molecules          2009          14          3952-3963
An Efficient Method for the N-Bromosuccinimide Catalyzed Synthesis of Indolyl-Nitroalkanes
Chun-Wei Kuo, Chun-Chao Wang, Hu-Lin Fang, B. R. Raju, Veerababurao Kavala, Pateliya M. Habib and Ching-Fa Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-¦Ã-¦Ã-dimethylallylindole
    ÏàËÆ¶È:71.4%
Journal of Natural Products          1986          Vol 49          534
3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia
A. O. Adeoye, B. O. Oguntimein, A. M. Clark, C. D. Hufford
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     N-acetyl-3-indolylmethylamine
    ÏàËÆ¶È:71.4%
Journal of Natural Products          1993          Vol 56          731
Metabolism of the Phytoalexin Brassinin by the "Blackleg" Fungus
M. Soledade, C. Pedras, Janet L. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound
C19H20N2O3S     ÏàËÆ¶È:71.4%
Heterocycles          2003          60          99-112
Regioselective Reduction of N-Alkyl-3-sulfonyl Glutarimide. Formal Synthesis of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Homobaclofen
Meng-Yang Chang and Shui-Tein Chen*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-(3-Indolyl)butanenitrile
C12H12N2O     ÏàËÆ¶È:71.4%
Phytochemistry          2010          71          1952-1962
Indolyl-3-acetaldoxime dehydratase from the phytopathogenic fungus Sclerotinia sclerotiorum: Purification, characterization, and substrate specificity
M. Soledade C. Pedras, Zoran Minic, Premila D. Thongbam, Vangala Bhaskar, Sabine Montaut
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     4-(Indol-3-ylmethylidene)-1,2-dimethylimidazol-5-one
C14H13N3O     ÏàËÆ¶È:71.4%
Tetrahedron          2012          68          5898-5907
Facile synthesis of 4-arylidene-5-imidazolinones as synthetic analogs of fluorescent protein chromophore
Cheng-Yu Lee, Yun-Chung Chen, Hao-Chun Lin, Yuandong Jhong, Chih-Wei Chang, Ching-Hua Tsai, Chai-Lin Kao, Tun-Cheng Chien
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1-Methyl-1,2,3,4-tetrahydro-¦Â-carboline-1,3-dicarboxylic Acid
    ÏàËÆ¶È:71.4%
Journal of Agricultural and Food Chemistry          1997          45          2458-2462
HPLC−MS/MS Profiling of Tryptophan-Derived Alkaloids in Food:  Identification of Tetrahydro-¦Â-carbolinedicarboxylic Acids
B. Gutsche and M. Herderich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     N-(indol-3-ylethyl)-2-hydroxy-3-methylpentanamide
C16H22N2O2     ÏàËÆ¶È:68.7%
Journal of Natural Products          1996          59          1157-1158
N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide, a Novel Indole Derivative from Xenorhabdus nematophilus
Jianxiong Li, Genhui Chen, and John M. Webster
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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