N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine
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N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine

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Category
BOC-Amino Acids
Catalog number
BAT-003177
CAS number
126613-96-5
Molecular Formula
C24H23NO4
Molecular Weight
389.44
N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine
IUPAC Name
(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyren-1-ylpropanoic acid
Synonyms
Boc-D-Ala(1-Pyn)-OH; Boc-D-Ala(1-Pyrenyl)-OH; BOC-3-(1-PYRENYL)-D-ALANINE
Purity
95%
InChI
InChI=1S/C24H23NO4/c1-24(2,3)29-23(28)25-19(22(26)27)13-17-10-9-16-8-7-14-5-4-6-15-11-12-18(17)21(16)20(14)15/h4-12,19H,13H2,1-3H3,(H,25,28)(H,26,27)
InChI Key
JDYATIJHVFTYFG-UHFFFAOYSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=C2C=CC3=CC=CC4=C3C2=C(C=C4)C=C1)C(=O)O

N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine, a specialized amino acid derivative, finds diverse applications in biochemical research and industry. Here are the key applications represented with high perplexity and burstiness:

Fluorescence Labeling: Acting as a potent fluorescent probe in biochemical assays, N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine emerges as a vital tool for tracking protein interactions and observing conformational changes in real-time. Researchers harness its exceptional pyrenyl group fluorescence to delve into binding events protein folding dynamics and enzymatic activities with acute precision.

Peptide Synthesis: Within the realm of peptide synthesis, this compound plays a pivotal role in infusing fluorescence properties into peptide chains. By integrating N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine into synthetic peptides, scientists unlock the ability to monitor peptide dynamics and interactions through the lens of fluorescence spectroscopy. This application proves invaluable for advancing drug development endeavors and delving into the intricacies of protein engineering.

Protein Structure Analysis: By incorporating N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine into proteins, researchers embark on a journey to explore protein structure and dynamics utilizing fluorescence methodologies. Leveraging its fluorescence characteristics, experts probe into protein folding stability conformational shifts under varying conditions, thereby unraveling essential insights into protein functionality and paving the way for designing therapeutic proteins with enhanced precision.

Environmental Monitoring: Highly sensitive to environmental alterations N-α-(t-Butoxycarbonyl)-β-(1-pyrenyl)-D-alanine steps into the realm of environmental monitoring as a potent biosensor. Its utility extends to detecting shifts in pH levels alterations in polarity or the presence of specific ions aiding in pollution evaluation and monitoring the effectiveness of environmental rehabilitation processes with exceptional acumen.

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