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1 .     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
2 .     (2'S,3'S)-N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide
C16H22N2O2     ÏàËÆ¶È:68.7%
Bulletin of the Korean Chemical Society          2003          24          623-626
Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC
Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (2'R,3'S)-N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide
C16H22N2O2     ÏàËÆ¶È:68.7%
Bulletin of the Korean Chemical Society          2003          24          623-626
Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC
Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Nb-acetyltryptamine
C12H14N2O     ÏàËÆ¶È:66.6%
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
5 .     N-fatty acyl trptamine
    ÏàËÆ¶È:62.5%
Phytochemistry          1993          34          1633-1635
N-fatty acyl tryptamines from Annona reticulata
Uki Maeda, Noriyuki Hara, Yoshinori Fujimoto, Anjani Srivastava, Yogesh Kumar Gupra, Mahendra Sahai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 13a
C14H16N2O3     ÏàËÆ¶È:60%
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
7 .     N-acetyl-tryptamine
C12H14N2O     ÏàËÆ¶È:60%
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
8 .     1-(1H-indol-3-yl)-2,3-dihydroxy-5-methyl-hexane
C15H21NO2     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2009          11          1040-1044
Steroids and alkaloids from the South China Sea sponge Axinella sp
Shu-Hua Qia, Yi-Fei Wangb and Si Zhanga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound
C19H20N2O3S     ÏàËÆ¶È:60%
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
10 .     3-(3-Indolyl)butanenitrile
C12H12N2O     ÏàËÆ¶È:60%
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
11 .     sattazolin
C15H19NO2     ÏàËÆ¶È:60%
The Journal of Antibiotics          1995          48          967-972
Sattabacins and Sattazolins: New Biologically Active Compounds with Antiviral Properties Extracted from a Bacillus sp.
GIORGIO LAMPIS, DELIA DEIDDA, CARLO MAULLU, MARIA A. MADEDDU, RAFFAELLO POMPEI, FRANCO DELLE MONACHE, GIUSEPPE SATTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     tetrahydro-2H-pyran-2-yl (2-(1H-indol-3-yl)ethyl)carbamodithioate
C16H20N2OS2     ÏàËÆ¶È:60%
Bulletin of the Korean Chemical Society          2012          33          4047-4051
A New and Facile Protocol for the Synthesis of Dithiocarbamate-linked 3,4-Dihydro-2H-pyran Using N-Halo Catalysts Under Mild Conditions Reaction
Ramin Ghorbani-Vaghei*, Mostafa Amiri, Hojat Veisi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     six-membered ring amide derivative
    ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          1993          41          1173-1176
The 1H- and 13C-Nuclear Magnetic Resonance Spectra of Manzamine C and Related Compounds
Hiroko SEKI,Masako NAKAGAWA,Akihiro HASHIMOTO and Tohru HINO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-(1-(2-Bromophenyl)-2-nitroethyl)-1H-indole
C16H13BrN2O2     ÏàËÆ¶È:56.2%
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
15 .     Nematophin
C16H20N2O2     ÏàËÆ¶È:56.2%
Bulletin of the Korean Chemical Society          2003          24          623-626
Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC
Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 23
    ÏàËÆ¶È:55.5%
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
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