Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609702Generated: October 30, 2026

L-Phenylalanine → L-Tyrosine

https://huagongshe.com/reaction/1609702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantTromethamine hydrochlorideHCID 93573—
ReactantPterinHCID 135398660—
Solvent2-amino-6,6-dimethyl-1,5,7,8-tetrahydropteridin-4-oneHCID 178428361—
ProductL-TyrosineHCID 6057—

Reaction Steps

Absorbance Spectrum of Quinoid-6,6-Me2PH2Generated by Phenylalanine Hydroxylase. Spectra were taken of the q-6,6-Me2PH2 synthesized enzymatically from 6,6-Me2PH4, and a comparison made with the chemically produced compound. The spectrophotometer was baseline corrected with sample and reference cuvettes containing all of the reaction components (0.1M Tris·HCl, pH 7.4, 4 mM phenylalanine, 2500 units catalase, 0.3 unit phenylalanine hydroxylase) except pterin in a total volume of 0.99 ml. 6,6-Me2PH4 (10 μl of 10 mM) was then added to the sample and distilled H2O (10 μl) to the reference cuvette. Scanning was begun immediately and spectra taken at 2 minute intervals. The formation of q-6,6-Me2PH2 was complete within 4 minutes. After correction for tyrosine formed and phenylalanine consumed, the spectrum was within 3% of that produced by Br2 oxidation of 6,6-Me2PH4 (FIGURE).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401844
Source datasetuspto-grants-1995_03
ORD IDord-a42c435ce5e9469ebaddcb6a3e0cf4b7
Source noteuspto-grants-1995_03