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J Antibiot (Tokyo) ; 57(1): 17-23, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15032481

ABSTRACT

The ethyl acetate extract of cultures of Janibacter limosus showed a high biological activity against bacteria, and fungi and delivered two new natural products, a tetrahydroquinoline derivative designated as helquinoline (1), and the N-acetylkynuramine (3a), along with other known secondary metabolites. The structure of 1 has been elucidated as 4-methoxy-2-methyl-1,2,3,4-tetrahydroquinoline-8-carboxylic acid on the basis of 1D and 2D NMR and mass spectra. The relative stereochemistry of the compound 1 was assigned as 2R*,4R* with the aid of coupling constants, NOESY correlation and by comparison with a related compound.


Subject(s)
Actinomycetales/metabolism , Anti-Bacterial Agents/isolation & purification , Kynuramine/analogs & derivatives , Quinolines/isolation & purification , Actinomycetales/chemistry , Anti-Bacterial Agents/biosynthesis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Fermentation , Kynuramine/chemistry , Kynuramine/pharmacology , Microbial Sensitivity Tests , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Quinolines/chemistry , Quinolines/pharmacology , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Stereoisomerism
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