β-(1,2,4-Triazol-1-yl)-DL-alanine
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β-(1,2,4-Triazol-1-yl)-DL-alanine

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Category
DL-Amino Acids
Catalog number
BAT-007507
CAS number
114419-45-3
Molecular Formula
C5H8N4O2
Molecular Weight
156.14
β-(1,2,4-Triazol-1-yl)-DL-alanine
IUPAC Name
2-amino-3-(1,2,4-triazol-1-yl)propanoic acid
Synonyms
H-DL-Ala(1,2,4-Triazol-1-yl)-OH; 2-Amino-3-(1H-1,2,4-triazol-1-yl)propanoic acid; H-BETA-(1,2,4-TRIAZOL-1-YL)-DL-ALA-OH; BETA-(1,2,4-TRIAZOL-1-YL)-DL-ALANINE; 3-(1H-1,2,4-Triazole-1-yl)-2-aminopropanoic acid
Related CAS
1219176-41-6 (labelled)
Appearance
Powder
Purity
97%
Density
1.620±0.10 g/cm3 (Predicted)
Boiling Point
402.9±55.0 °C (Predicted)
InChI
InChI=1S/C5H8N4O2/c6-4(5(10)11)1-9-3-7-2-8-9/h2-4H,1,6H2,(H,10,11)
InChI Key
XVWFTOJHOHJIMQ-UHFFFAOYSA-N
Canonical SMILES
C1=NN(C=N1)CC(C(=O)O)N

β-(1,2,4-Triazol-1-yl)-DL-alanine, a versatile chemical compound with diverse applications in bioscience research and pharmaceutical development, finds its utility in various domains. Here are the key applications presented with high perplexity and burstiness:

Structural Biology: Serving as a potent probe in structural biology, β-(1,2,4-Triazol-1-yl)-DL-alanine emerges as a key player in unraveling intricate protein-ligand interactions. By integrating this compound into peptide sequences, researchers embark on a journey to dissect the structural conformation and binding properties of proteins, shedding light on their nuanced functionalities and aiding in the development of cutting-edge therapeutic agents.

Drug Design and Development: Positioned at the forefront of pharmaceutical innovation, β-(1,2,4-Triazol-1-yl)-DL-alanine takes center stage as a foundational element for synthesizing novel drug candidates. Leveraging its unique structural configuration, scientists venture into the realm of designing molecules endowed with specific pharmacological attributes, be it as enzyme inhibitors or receptor modulators. This transformative process fuels the quest for groundbreaking drugs tailored to combat a myriad of diseases on the medical horizon.

Antimicrobial Research: Posing as a potent contender in the realm of antimicrobial exploration, β-(1,2,4-Triazol-1-yl)-DL-alanine's triazole moiety unlocks a realm of possibilities in combating microbial pathogens. Researchers embark on a mission to assess its efficacy against diverse microbial foes, unveiling its mechanism of action in the process. This quest for novel antimicrobial therapies couldn't come at a more crucial time as the specter of drug resistance looms large, propelling the need for innovative solutions to the forefront.

Chemical Biology: In the realm of chemical biology, β-(1,2,4-Triazol-1-yl)-DL-alanine emerges as a linchpin in dissecting enzyme activities and metabolic pathways. Whether acting as a substrate or an inhibitor in diverse biochemical assays, this compound offers invaluable insights into the specificities of enzymes and the catalytic mechanisms at play. Such revelations stand as pillars supporting both fundamental research endeavors and the evolution of industrial biocatalysts, shaping the landscape of biotechnological advancements.

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