β-(4-Thiazolyl)-DL-alanine
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β-(4-Thiazolyl)-DL-alanine

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Category
DL-Amino Acids
Catalog number
BAT-007524
CAS number
14717-97-6
Molecular Formula
C6H8N2O2S
Molecular Weight
172.21
β-(4-Thiazolyl)-DL-alanine
IUPAC Name
2-amino-3-(1,3-thiazol-4-yl)propanoic acid
Synonyms
H-DL-Ala(4-Thz)-OH; H-DL-Ala(4-Thiazolyl)-OH; 2-Amino-3-(thiazol-4-yl)propanoic acid; L-4-Thiazolylalanine; 2-amino-3-(4-thiazolyl)-propanoic acid; d-3-(4-thiazolyl)-alanine; 3-(1,3-Thiazol-4-yl)alanine; L-3-(4-Thiazolyl)-alanine; 3-(4-Thiazolyl)-DL-alanine; beta-(4-Thiazolyl)-DL-alanine; DL-4-Thiazolylalanine; 4-Thiazolealanine; 3-Thiazol-4-yl-L-alanine
Appearance
Powder
Purity
97%
Density
1.433 g/cm3
Melting Point
237 °C
Boiling Point
353.3 °C at 760 mmHg
InChI
InChI=1S/C6H8N2O2S/c7-5(6(9)10)1-4-2-11-3-8-4/h2-3,5H,1,7H2,(H,9,10)
InChI Key
WBZIGVCQRXJYQD-UHFFFAOYSA-N
Canonical SMILES
C1=C(N=CS1)CC(C(=O)O)N

β-(4-Thiazolyl)-DL-alanine, a compound of considerable significance in biochemical and pharmacological realms, finds diverse applications. Here are the key applications narrated with high perplexity and burstiness:

Antibacterial Research: Delving into the antibacterial realm, researchers investigate the potent antibacterial properties of β-(4-Thiazolyl)-DL-alanine, positioning it as a potential lead in novel antibiotic development. By probing its intricate mode of action against diverse bacterial strains, scientists aim to unveil innovative therapeutic strategies to combat the rising threat of antibiotic-resistant infections. This compound emerges as a beacon of hope in the ongoing battle against microbial adversaries.

Enzyme Inhibition Studies: Within the domain of enzyme inhibition studies, β-(4-Thiazolyl)-DL-alanine takes center stage, offering a glimpse into its interactions with specific bacterial enzymes. Through the inhibition of these enzymatic catalysts, β-(4-Thiazolyl)-DL-alanine disrupts crucial bacterial cell wall synthesis and metabolic pathways. These deep-rooted insights serve as the cornerstone for crafting targeted antibacterial agents endowed with precision and efficacy, shaping the future of antibacterial therapeutics.

Pharmacological Testing: Driving progress in pharmacological laboratories, β-(4-Thiazolyl)-DL-alanine emerges as a pivotal tool for screening potential drug candidates. Leveraging its structural nuances, researchers harness this compound as a model substrate in a myriad of drug discovery assays. This strategic utilization aids in pinpointing and nurturing novel pharmaceutical compounds characterized by enhanced efficacy and safety profiles, steering the course of pharmaceutical innovation towards new horizons.

Biochemical Assays: In the intricate realm of biochemical research, β-(4-Thiazolyl)-DL-alanine plays a pivotal role in diverse assays aimed at unraveling enzyme kinetics and substrate interactions. With its unique chemical blueprint, this compound serves as a versatile substrate or inhibitor in enzymatic reactions, shedding light on the intricate mechanisms underlying biochemical processes. This application not only illuminates the detailed workings of enzymes, but also guides researchers in optimizing assay conditions for enhanced research efficacy, laying the foundation for groundbreaking discoveries in the biochemical landscape.

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