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Sku CI05232_1_G
Chem Impex
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Product Information

Product Name
L-3-Methoxyphenylalanine
Brand Name
Chem Impex
Product Number
05232
CAS
33879-32-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
10943394
IUPAC Name
(2S)-2-amino-3-(3-methoxyphenyl)propanoic acid
InChI Key
XTXGLOBWOMUGQB-VIFPVBQESA-N
SMILES
COC1=CC=CC(=C1)CC@@H(C(=O)O)N

Application

L-3-Methoxyphenylalanine is widely utilized in research focused on:

Neuroscience Research: This compound is studied for its potential effects on neurotransmitter systems, particularly in understanding mood disorders and neurodegenerative diseases.

Pharmaceutical Development: It serves as a building block in the synthesis of novel drugs, especially those targeting metabolic pathways and neurological functions.

Biochemical Studies: Researchers use it to investigate protein interactions and enzyme activities, providing insights into cellular processes and disease mechanisms.

Food Industry: Its properties are explored in the development of flavor enhancers or nutritional supplements, appealing to health-conscious consumers.

Cosmetic Formulations: The compound is examined for its antioxidant properties, making it a candidate for skin care products aimed at improving skin health and appearance.

References

Author Correction: Efficient genetic code expansion without host genome modifications

Publication Name: Nature Biotechnology
Publication Date: 2024-09-11
DOI: 10.1038/s41587-024-02385-y|10.1038/s41587-024-02454-2

Phenylalanine ammonia-lyases: combining protein engineering and natural diversity

Publication Name: Applied Microbiology and Biotechnology
Publication Date: 2023-01-20
DOI: 10.1007/s00253-023-12374-x

Enzymatic cascade systems for D-amino acid synthesis: progress and perspectives

Publication Name: Systems Microbiology and Biomanufacturing
Publication Date: 2021-06-16
DOI: 10.1007/s43393-021-00037-9

Influence of Momordica charantia on oxidative stress-induced perturbations in brain monoamines and plasma corticosterone in albino rats

Publication Name: Indian Journal of Pharmacology
Publication Date: 2011-07
DOI: 10.4103/0253-7613.83114

Synthesis of 6- or 7-substituted 1,2,3,4-tetrahydroisoquinoline- 3-carboxylic acids

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 1999-03
DOI: 10.1007/bf02443634|10.1023/a:1008826909441