H-Tyr-OMe

H-Tyr-OMe is an endogenous metabolite. H-Tyr-OMe quenches the fluorescence of carbon dots by oxidizing the phenolic hydroxyl group to quinone under the catalysis of Tyrosinase, and its amino and thiol binding ability can respond to changes in the concentration of biothiols[1][2].

Product Specifications

CAS Number

[1080-06-4]

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Endogenous Metabolite; Tyrosinase

Type

Natural Products

Related Pathways

Metabolic Enzyme/Protease

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/h-tyr-ome.html

Purity

99.92

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

N[C@H](C(OC)=O)CC1=CC=C(O)C=C1

Molecular Formula

C10H13NO3

Molecular Weight

195.22

Precautions

H302, H315, H319, H335

References & Citations

[1]B.Korbélya, et al. Amino acids and their Cu complexes covalently grafted onto a polystyrene resin-A vibrational spectroscopic study. Journal of Molecular Structure. Volumes 834-836, 27 May 2007, Pages 345-348.|[2]Zhu H, et al. L-tyrosine methyl ester-stabilized carbon dots as fluorescent probes for the assays of biothiols. Anal Chim Acta. 2018 May 2;1006:83-89.