N-α-Phenoxycarbonyl-L-alanine
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N-α-Phenoxycarbonyl-L-alanine

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Category
L-Amino Acids
Catalog number
BAT-002134
CAS number
141695-27-4
Molecular Formula
C10H11NO4
Molecular Weight
209.20
Synonyms
Ala-NPC

N-α-Phenoxycarbonyl-L-alanine, a specialized compound with diverse biochemical and pharmaceutical applications, plays pivotal roles in various fields. Here are the key applications, presented with high perplexity and burstiness:

Peptide Synthesis: In the realm of solid-phase peptide synthesis, N-α-Phenoxycarbonyl-L-alanine emerges as a crucial player, serving as a shielded amino acid. The phenoxycarbonyl group acts as a guardian, protecting the amino group throughout peptide bond formation, thereby thwarting unwanted side reactions. This meticulous process ensures the production of pure peptides of utmost quality, indispensable for both research endeavors and therapeutic advancements.

Enzyme Inhibition Studies: Delving into enzyme activity modulation, this compound showcases its prowess as a potent inhibitor. By mimicking a competitive substrate or inhibitor, N-α-Phenoxycarbonyl-L-alanine aids researchers in unraveling the intricacies of enzyme kinetics and mechanistic pathways. This profound understanding forms the bedrock for designing novel enzyme-targeted medications and biocatalysts, driving forward the frontiers of biochemical research.

Chiral Synthesis: The art of chiral synthesis finds a valuable ally in N-α-Phenoxycarbonyl-L-alanine, a key ingredient in crafting enantiomerically pure compounds essential for pharmaceutical and agrochemical industries. The chiral center within this compound ensures the precise stereochemistry of synthesized products, a critical factor in producing drugs and agents with tailored biological activities. Through this intricate process, the synthesis of compounds with desired properties is elevated to an art form, revolutionizing pharmaceutical research.

Protein Structure Analysis: Stepping into the domain of structural biology, N-α-Phenoxycarbonyl-L-alanine takes center stage by integrating into proteins to streamline their crystallization and subsequent X-ray diffraction studies. This strategic modification aids in unraveling the intricate structure of proteins, shedding light on the relationship between structure and function. Such profound insights are paramount in drug development and deciphering the underlying mechanisms of fundamental biological processes, paving the way for groundbreaking discoveries.

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