N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine
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N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine

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Category
BOC-Amino Acids
Catalog number
BAT-005059
CAS number
21012-18-0
Molecular Formula
C11H17N3O4
Molecular Weight
255.27
N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyrazol-1-ylpropanoic acid
Synonyms
Boc-Ala(1-Pyz)-OH; Boc-Ala(1-Pyrazolyl)-OH; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyrazol-1-ylpropanoic acid; l-n-boc-3-pyrazol-1-yl-alanine; N-Boc-3-pyrazol-1-yl-Ala
Purity
≥ 95%
Density
1.260 g/cm3
Boiling Point
441.9 °C at 760 mmHg
InChI
InChI=1S/C11H17N3O4/c1-11(2,3)18-10(17)13-8(9(15)16)7-14-6-4-5-12-14/h4-6,8H,7H2,1-3H3,(H,13,17)(H,15,16)/t8-/m0/s1
InChI Key
JPGQESMEFISORC-QMMMGPOBSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CN1C=CC=N1)C(=O)O

N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine, a specialized amino acid derivative, finds diverse applications in biochemical research and pharmaceutical development. Here are the key applications presented with high perplexity and burstiness:

Peptide Synthesis: Acting as a protected amino acid, N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine plays a vital role in solid-phase peptide synthesis, enabling the construction of intricate peptides and proteins. The t-butoxycarbonyl group acts as a safeguarding entity for the amino functionality, preventing undesired side reactions and ensuring precision in the synthesis process. This meticulous approach results in elevated yields and elevated purity levels of the desired peptides, facilitating advanced research in peptide chemistry.

Enzyme Inhibition Studies: Researchers leverage this compound to craft enzyme inhibitors tailored for investigative purposes. By incorporating it into peptide sequences, scientists can explore its effects on enzyme activity, particularly focusing on enzymes that recognize pyrazolyl-containing substrates. These studies are pivotal for elucidating enzyme kinetics and advancing the development of novel therapeutic agents, pushing the boundaries of enzymology.

Drug Design and Development: Within the realm of medicinal chemistry, N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine emerges as a valuable tool for designing cutting-edge pharmaceuticals. Its unique structural attributes open doors for exploring novel interactions with biological targets such as receptors or enzymes. This exploration can lead to the unearthing of compounds with distinct pharmacological properties, ushering in a new era of therapeutic innovation filled with possibilities and groundbreaking discoveries.

Structural Biology: In the intricate field of structural biology, this compound serves as a fundamental component in crystallography studies, aimed at unraveling the three-dimensional structure of proteins and protein-ligand complexes. Through the strategic modification of peptides or proteins with N-α-t-Butoxycarbonyl-β-(1-pyrazolyl)-L-alanine, researchers gain comprehensive insights into binding interactions and conformational changes. This invaluable information plays a pivotal role in rational drug design and enhances our comprehension of the intricate molecular mechanisms underlying biological processes, paving the way for innovative advancements in structural biology and drug discovery.

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