Über die Umwandlung der 3-Hydroxy-anthranilsäure in Chinolinsäure und Nicotinsäure im tierischen Organismus II. Die Isolierung und vorläufige Charakterisierung des primären Oxydationsproduktes der 3-Hydroxy-anthranilsäure
- 1 January 1957
- journal article
- research article
- Published by Walter de Gruyter GmbH in Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie
- Vol. 306 (Jahresband), 145-153
- https://doi.org/10.1515/bchm2.1957.306.1-2.145
Abstract
The primary enzymatic cleavage product of 3-hydroxyanthranilic acid was isolated as 2,4-dinitrophenylhydrazone. The cleavage product is regarded as l-amino-4-formyl-l,3-butadien-l,2-dicarboxylic acid. Two substances were isolated in the form of crystalline dinitrophenylhydra-zones after mild hydrogenation of the primary enzymatic cleavage product. The UV absorption spectra show the typical characteristics associated with dinitrophenylhydrazone-amino compounds. The infrared spectrum of substance A points to a dinitrophenylhydrazone-amino acid structure.Keywords
This publication has 3 references indexed in Scilit:
- STUDIES OF THE ENZYMATIC TRANSFORMATION OF 3-HYDROXYANTHRANILATE TO QUINOLINATEJournal of Biological Chemistry, 1954
- 3-Hydroxyanthranilic acid metabolism. IV. Spectrophotometric evidence for the formation of an intermediateArchives of Biochemistry and Biophysics, 1951
- The terminal peptides of insulinBiochemical Journal, 1949