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Sku CI07376_1_G
Chem Impex
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Product Information

Product Name
3-(4-Thiazolyl)-L-alanine
Brand Name
Chem Impex
Product Number
07376
CAS
119433-80-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2761495
IUPAC Name
(2S)-2-amino-3-(1,3-thiazol-4-yl)propanoic acid
InChI Key
WBZIGVCQRXJYQD-YFKPBYRVSA-N
SMILES
C1=C(N=CS1)CC@@H(C(=O)O)N

Description

3-(4-Thiazolyl)-L-alanine is widely utilized in research focused on:

Pharmaceutical Development: This compound is explored for its potential as a building block in the synthesis of novel drugs, particularly in targeting specific diseases due to its unique thiazole structure.

Biochemical Research: It serves as a valuable tool in studying protein interactions and enzyme activities, helping researchers understand metabolic pathways and cellular functions.

Agricultural Chemistry: The compound is investigated for its role in developing bioactive agents that can enhance plant growth or provide resistance against pests and diseases.

Food Industry: Its potential as a flavor enhancer or preservative is being studied, offering a natural alternative to synthetic additives in food products.

Cosmetic Formulations: Researchers are exploring its use in skincare products for its antioxidant properties, which may help in protecting skin from oxidative stress.

References Data Source From Pubchem

Rapid de novo discovery of peptidomimetic affinity reagents for human angiotensin converting enzyme 2

Publication Name: Communications Chemistry
Publication Date: 2022-01-19
DOI: 10.1038/s42004-022-00625-3

Separation of Enantiomers of N-Protected Non-Protein Amino Acid Esters by Chiral High-Performance Liquid Chromatography

Publication Name: Chromatographia
Publication Date: 2004-09-13
DOI: 10.1365/s10337-004-0388-4

Separation of Enantiomers of Non-Protein Amino Acids by High-Performance Liquid Chromatography on a Chiral Ligand-Exchange Column

Publication Name: Chromatographia
Publication Date: 2004-06-18
DOI: 10.1365/s10337-004-0298-5

Application of hexafluoroacetone as protecting and activating reagent in amino acid and peptide chemistry

Publication Name: Amino Acids
Publication Date: 1995-06
DOI: 10.1007/bf00806492