Issue 105, 2014

Phenylalanine iminoboronates as new phenylalanine hydroxylase modulators

Abstract

Herein we report the discovery of new modulators of human phenylalanine hydroxylase (hPAH) inspired by the structure of its substrate and regulator L-phenylalanine. These new hPAH modulators were simply prepared in good-to-excellent yields and excellent diastereoselectivities, based on a boron promoted assembly of L-phenylalanine, salicylaldehyde and aryl boronic acids. Iminoboronate 8, prepared with L-phenylalanine, para-methoxy-salicylaldehyde and phenyl boronic acid, was identified as the most efficient hPAH modulator, with an apparent binding affinity nearly identical to the natural allosteric activator L-phenylalanine.

Graphical abstract: Phenylalanine iminoboronates as new phenylalanine hydroxylase modulators

Supplementary files

Article information

Article type
Paper
Submitted
12 Sep 2014
Accepted
05 Nov 2014
First published
06 Nov 2014

RSC Adv., 2014,4, 61022-61027

Author version available

Phenylalanine iminoboronates as new phenylalanine hydroxylase modulators

F. Montalbano, J. Leandro, G. D. V. F. Farias, P. R. Lino, R. C. Guedes, J. B. Vicente, P. Leandro and P. M. P. Gois, RSC Adv., 2014, 4, 61022 DOI: 10.1039/C4RA10306H

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