Acetyl-L-tyrosine amide|02640|1948-71-6

Acetyl-L-tyrosine amide

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Sku CI02640_1_G
Chem Impex
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Product Information

Product Name
Acetyl-L-tyrosine amide
Brand Name
Chem Impex
Product Number
02640
CAS
1948-71-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
735956
IUPAC Name
(2S)-2-acetamido-3-(4-hydroxyphenyl)propanamide
InChI Key
RJNKBEQRBIJDNM-JTQLQIEISA-N
SMILES
CC(=O)NC@@H(CC1=CC=C(C=C1)O)C(=O)N

Application

Acetyl-L-tyrosine amide is widely utilized in research focused on:

Nutritional Supplements: This compound is often included in dietary supplements aimed at enhancing cognitive function and mental performance, making it popular among students and professionals seeking to boost focus and memory.

Neurotransmitter Support: It serves as a precursor to neurotransmitters, particularly dopamine, which is crucial for mood regulation and motivation. This application is beneficial in the development of products aimed at improving mental health.

Sports Nutrition: Athletes use this compound to potentially enhance physical performance and recovery, as it may help in reducing fatigue and improving endurance during intense training sessions.

Pharmaceutical Research: Researchers explore its potential in developing therapies for conditions like depression and anxiety, leveraging its role in neurotransmitter synthesis to create innovative treatment options.

Cosmetic Formulations: Its antioxidant properties make it a valuable ingredient in skincare products, helping to protect the skin from oxidative stress and promoting overall skin health.

References Data Source From Pubchem

Bilateral Effects of Excipients on Protein Stability: Preferential Interaction Type of Excipient and Surface Aromatic Hydrophobicity of Protein
Publication Name: Pharmaceutical Research
Publication Date: 2017-04-11
DOI: 10.1007/s11095-017-2152-0

Preferential interactions between protein and arginine: Effects of arginine on tertiary conformational and colloidal stability of protein solution
Publication Name: International Journal of Pharmaceutics
Publication Date: 2015-01-30
DOI: 10.1016/j.ijpharm.2014.12.038

The kinetics of the reaction of nitrogen dioxide with iron(II)- and iron(III) cytochrome c
Publication Name: Free Radical Biology and Medicine
Publication Date: 2014-04
DOI: 10.1016/j.freeradbiomed.2014.01.014

A novel, volumizing cosmetic formulation significantly improves the appearance of target Glabellar lines, nasolabial folds, and crow's feet in a double-blind, vehicle-controlled clinical trial
Publication Name: Journal of drugs in dermatology : JDD
Publication Date: 2014-01

Influence of the charge of amino group on rate and direction of intramolecular electron transfer reaction in shortlived oxidized peptides containing tryptophan and tyrosine
Publication Name: Doklady Physical Chemistry
Publication Date: 2013-10-23
DOI: 10.1134/s0012501613100023