Tyrosine
Tyrosine
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Tyrosine

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Catalog Number PR556025
CAS 556-02-5
Synonyms D-tyrosine
IUPAC Name (2R)-2-amino-3-(4-hydroxyphenyl)propanoic acid
Molecular Weight 181.19
Molecular Formula C9H11NO3
InChI OUYCCCASQSFEME-MRVPVSSYSA-N
InChI Key InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1
Associated Therapies Amino acid supplementation
Drug Categories Amino Acids; Amino Acids, Aromatic; Amino Acids, Cyclic; Amino Acids, Peptides, and Proteins; Dietary Supplements; Proteinogenic Amino Acids; Supplements
Drug Interactions Levodopa-Tyrosine may increase the excretion rate of Levodopa which could result in a lower serum level and potentially a reduction in efficacy.
Isomeric SMILES C1=CC(=CC=C1C[C@H](C(=O)O)N)O
Standard In-house
Type Small Molecule
Therapeutic Category Ophthalmic Agents
Pharmacology

Indications

Tyrosine is proposed to have several clinical applications, primarily relating to mood and cognitive functions. Although it is purported to have antidepressant properties, research outcomes have been inconsistent. Additionally, claims suggest that tyrosine may alleviate stress and address symptoms of narcolepsy and chronic fatigue, although these assertions have been challenged by some studies.

Pharmacodynamics

As a nonessential amino acid, tyrosine is synthesized in the human body from phenylalanine. It is integral to the formation of proteins, enzymes, and muscle tissue. Functioning as a precursor to key neurotransmitters such as norepinephrine and dopamine, tyrosine is thought to positively influence mood and cognitive functions, potentially improving memory and enhancing mental alertness. Furthermore, it is critical in the production of melanin and thyroid hormones like thyroxin. Deficiencies in tyrosine can lead to hypothyroidism, low blood pressure, and decreased body temperature. Supplementation has been explored for mitigating stress and symptoms associated with narcolepsy and chronic fatigue.

Absorption

L-tyrosine is absorbed through the small intestine predominantly via a sodium-dependent active transport mechanism. This method ensures its efficient uptake into the bloodstream, facilitating its subsequent distribution and utilization within the body.

Metabolism

Upon entering the liver, L-tyrosine participates in various biochemical pathways, including those involved in protein synthesis and oxidative catabolic processes. Tyrosine that is not metabolized in the liver circulates throughout the body, enabling its uptake by different tissues as needed for physiological functions.

Mechanism of Action

The mechanism by which tyrosine exerts its effects is primarily linked to its role as a precursor in neurotransmitter biosynthesis. Tyrosine is synthesized within cells through the hydroxylation of phenylalanine, an essential amino acid. This biosynthetic pathway is analogous to the conversion of methionine to cysteine. Approximately half of the body's phenylalanine intake is utilized for tyrosine production. Moreover, dietary intake of tyrosine can reduce the need for phenylalanine by around 50%. L-tyrosine's potential antidepressant activity is attributed to its critical role in the production of the neurotransmitters norepinephrine and dopamine. Increased levels of these neurotransmitters in the brain are believed to be linked to the alleviation of depressive symptoms.

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