N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine
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N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine

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Category
BOC-Amino Acids
Catalog number
BAT-005213
CAS number
270596-44-6
Molecular Formula
C17H23NO4
Molecular Weight
305.37
N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine
IUPAC Name
(E,3S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-6-phenylhex-5-enoic acid
Synonyms
Boc-Ala(Styryl)-(C#CH2)OH; Boc-Phe(#5,6=CH)-(C#CH2)OH; (S)-3-[(t-Butoxycarbonyl)amino]-6-phenyl-5-hexenoic acid; Boc-(S)-3-amino-6-phenyl-5-hexenoic acid
Purity
≥ 95%
Density
1.131 g/cm3
Boiling Point
507.2±50.0 °C
InChI
InChI=1S/C17H23NO4/c1-17(2,3)22-16(21)18-14(12-15(19)20)11-7-10-13-8-5-4-6-9-13/h4-10,14H,11-12H2,1-3H3,(H,18,21)(H,19,20)/b10-7+/t14-/m0/s1
InChI Key
ZEIROKVMYFFJKQ-RNVIBTMRSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC=CC1=CC=CC=C1)CC(=O)O

N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine, an amino acid derivative with specialized applications in scientific research and biochemistry, offers unique possibilities for innovation. Delve into its key applications presented with high perplexity and burstiness.

Peptide Synthesis: Utilizing N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine as a foundational element in peptide synthesis unlocks avenues for integrating non-natural amino acids into peptides and proteins. Its exceptional structure invites exploration of unconventional peptide conformations and functionalities, sparking the creation of novel therapeutics and biochemicals with distinct properties.

Protein Engineering: Scientists harness the power of N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine to instigate targeted structural alterations in proteins. By introducing this amino acid derivative, researchers can sculpt proteins with modified folding behaviors, stability, or activity levels. This strategy serves as a valuable tool for investigating protein functionalities and crafting proteins with enhanced or unique attributes.

Drug Design: Infusing N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine into peptide-based drug candidates elevates their pharmacokinetic and pharmacodynamic characteristics. The distinct chemical composition of this amino acid derivative enhances the stability and bioaccessibility of peptide drugs, enriching the toolkit for optimizing and designing cutting-edge therapeutic agents.

Molecular Probes: Embark on the frontier of biological exploration with N-β-(t-Butoxycarbonyl)-γ-styryl-L-β-homoalanine, a catalyst for developing molecular probes in the study of biological systems. Leveraging its unique chemical attributes, researchers can craft probes that emit fluorescence or other detectable signals in biochemical assays. These probes play a pivotal role in visualizing and quantifying biomolecular interactions and functions across diverse research realms, facilitating deeper insights into complex biological processes.

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