Abstract
THE formation of a red pigment from indole and pyridoxal interferes in the enzymatic determination of L-tryptophan1. On the basis of the following evidence, it is proposed that the pigment has the structure IIa shown in Fig. 1 and is therefore analogous to the rosein-doles of Fischer2.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Scott, T. A., Biochem. J., 80, 462 (1961).
Fischer, E., and Wagner, P., Ber., 20, 815 (1887).
Sumpter, W. C., and Miller, F. M., Heterocyclic Compounds with Indole and Carbazole Systems, 203 (Interscience, 1954).
Harley Mason, J., and Bullock, J. D., Biochem. J., 51, 430 (1952).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
SCOTT, T. A Reaction of Pyridoxal with C-3 Unsubstituted Indoles. Nature 204, 77–79 (1964). https://doi.org/10.1038/204077a0
Issue Date:
DOI: https://doi.org/10.1038/204077a0
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.