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

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Category
BOC-Amino Acids
Catalog number
BAT-005212
CAS number
332064-73-0
Molecular Formula
C17H23NO4
Molecular Weight
305.37
N-β-(t-Butoxycarbonyl)-γ-styryl-D-β-homoalanine
IUPAC Name
(E,3R)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-6-phenylhex-5-enoic acid
Synonyms
Boc-D-Ala(Styryl)-(C#CH2)OH; Boc-D-Phe(#5,6=CH)-(C#CH2)OH; (R)-3-[(t-Butoxycarbonyl)amino]-6-phenyl-5-hexenoic acid; (2R)-3-amino-2-[(2-methylpropan-2-yl)oxycarbonyl]-6-phenylhex-5-enoic acid; 5-Hexenoic acid,3-[[(1,1-dimethylethoxy)carbonyl]amino]-6-phenyl-,(3R); N-T-BUTOXYCARBONYL-(R)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID; Boc-D-b-HoAla(styryl)-OH; BOC-(R)-3-AMINO-(6-PHENYL)-5-HEXENOIC ACID; Boc-styryl-D-β-homoalanine; Boc-D-β-HomoAla(styryl)-OH
Appearance
White powder
Purity
≥ 99% (HPLC)
Density
1.131 g/cm3
Melting Point
108-114 °C
Storage
Store at 2-8 °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-/m1/s1
InChI Key
ZEIROKVMYFFJKQ-DNGMOHDESA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC=CC1=CC=CC=C1)CC(=O)O

N-β-(t-Butoxycarbonyl)-γ-styryl-D-β-homoalanine, an innovative synthetic amino acid derivative, holds a plethora of applications within the bioscience industry. Here are the key applications, intricately presented with a high degree of perplexity and burstiness:

Peptide Synthesis: Embracing the potential of N-β-(t-Butoxycarbonyl)-γ-styryl-D-β-homoalanine, scientists can intricately incorporate this distinct compound into synthetic peptides, unraveling the complexities of protein structure and function. Its chemical intricacy serves as a powerful instrument for introducing targeted modifications in peptide sequences, unveiling profound insights into protein interactions and catalyzing the development of novel therapeutic peptides endowed with heightened stability and efficacy.

Drug Design and Development: Spearheading pharmaceutical innovation, this compound serves as a cornerstone in the formulation of groundbreaking drugs. Its unparalleled characteristics empower researchers to craft enzyme inhibitors or receptor agonists with unmatched specificity and potency, propelling the exploration for novel drug discoveries and refining existing treatments through a maze of possibilities.

Molecular Probes: Unleashing the potential of N-β-(t-Butoxycarbonyl)-γ-styryl-D-β-homoalanine, scientists can forge fluorescent molecular probes that redefine the landscape of imaging and diagnostics. By coupling these derivatives with luminous tags, researchers can unveil the intricacies of biochemical processes in a dynamic, real-time spectacle, offering a profound edge in cellular biology exploration and the tracking of disease progression in the realm of clinical diagnostics.

Proteomics Research: Integrating N-β-(t-Butoxycarbonyl)-γ-styryl-D-β-homoalanine into the intricate realm of proteins unveils a treasure trove of insights into post-translational modifications and protein-protein interactions. By replacing select amino acids with this versatile derivative, researchers embark on a journey to probe the impact of structural metamorphoses on protein functionality, thus illuminating the intricate landscape of complex biological systems and uncovering novel therapeutic targets, echoing the symphony of life's enigmatic mechanisms.

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