N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine
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N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine

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Category
BOC-Amino Acids
Catalog number
BAT-005199
CAS number
219297-11-7
Molecular Formula
C19H23NO4
Molecular Weight
329.39
N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine
IUPAC Name
(3S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-naphthalen-2-ylbutanoic acid
Synonyms
Boc-Ala(2-Naph)-(C#CH2)OH; Boc-Nal(2)-(C#CH2)OH; (S)-3-[(t-Butoxycarbonyl)amino]-4-(2-naphthyl)butanoic acid; Boc-(S)-3-amino-4-(2-naphthyl)-butyric acid
Purity
≥ 95%
Density
1.179 g/cm3
Boiling Point
527.9 °C at 760 mmHg
InChI
InChI=1S/C19H23NO4/c1-19(2,3)24-18(23)20-16(12-17(21)22)11-13-8-9-14-6-4-5-7-15(14)10-13/h4-10,16H,11-12H2,1-3H3,(H,20,23)(H,21,22)/t16-/m0/s1
InChI Key
RKULNBHGHIPRGC-INIZCTEOSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC2=CC=CC=C2C=C1)CC(=O)O

N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine, a specialized chemical compound with diverse applications in biochemical research and pharmaceutical development, presents a rich tapestry of opportunities for exploration. Here are the key applications of N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine depicted with a high degree of perplexity and burstiness:

Peptide Synthesis: Embedded in the intricate realm of biochemistry, N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine assumes a pivotal role in the complex synthesis of peptides and proteins. This compound serves as a shielded amino acid, cloaked by the protective t-butoxycarbonyl (Boc) group during peptide chain assembly, ensuring impeccable fidelity in synthesis. The outcome is the generation of biologically active peptides, holding profound implications for both research and therapeutic ventures.

Structure-Activity Relationship (SAR) Studies: Venturing into the pharmaceutical domain, this compound emerges as a crucial figure in deciphering the influence of molecular structure on biological activity. By incorporating N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine into peptide sequences, researchers can refine and amplify interactions with target proteins or receptors, unveiling crucial insights for the development of potent and selective drugs.

Protein-Protein Interaction Studies: Shedding light on the mysteries of protein-protein interactions, N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine acts as a catalyst for crafting modified peptides that uncover the intricacies of these processes. These specialized peptides mimic specific protein segments, unveiling binding sites, affinities, and the dynamic nature of interactions. Such revelations are paramount for understanding cellular dynamics and pinpointing strategic intervention points within disease pathways.

Chemical Biology: Spearheading the forefront of chemical biology, N-β-(t-Butoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine empowers researchers in the design and synthesis of novel bioactive molecules. Providing chemists with the ability to finely adjust molecular architectures, this compound offers a nuanced perspective of biological systems with meticulous control. Harnessing the potential of these compounds, scientists can delve deeper into biological mechanisms, paving the way for innovative therapeutic modalities.

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