γ-(2-Naphthyl)-D-β-homoalanine hydrochloride
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γ-(2-Naphthyl)-D-β-homoalanine hydrochloride

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Category
β−Amino Acids
Catalog number
BAT-002557
CAS number
331847-02-0
Molecular Formula
C14H16ClNO2
Molecular Weight
265.74
IUPAC Name
(3R)-3-amino-4-naphthalen-2-ylbutanoic acid;hydrochloride
Synonyms
(R)-3-Amino-4-(2-naphthyl)-butyric acid HCl; H-D-β-HomoAla(2-naphthyl)-OH HCl
Appearance
White Powder
Purity
≥ 99% by HPLC
Melting Point
238-245 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C14H15NO2.ClH/c15-13(9-14(16)17)8-10-5-6-11-3-1-2-4-12(11)7-10;/h1-7,13H,8-9,15H2,(H,16,17);1H/t13-;/m1./s1
InChI Key
BWSJJEOZKOCDCT-BTQNPOSSSA-N
Canonical SMILES
C1=CC=C2C=C(C=CC2=C1)CC(CC(=O)O)N.Cl

γ-(2-Naphthyl)-D-β-homoalanine hydrochloride, a specialized chemical compound, plays a pivotal role in pharmaceutical research, medicinal chemistry, and biochemical studies. Here are the key applications presented with high perplexity and burstiness:

Drug Development: With its distinct structural attributes, γ-(2-Naphthyl)-D-β-homoalanine hydrochloride emerges as a cornerstone in the quest for novel therapeutic agents. Researchers leverage its unique properties for synthesizing peptidomimetics and diverse pharmaceutical compounds, exploring uncharted drug targets, and fine-tuning pharmacodynamic and pharmacokinetic profiles for enhanced efficacy.

Peptide Chemistry: Within the domain of peptide chemistry, γ-(2-Naphthyl)-D-β-homoalanine hydrochloride stands out as a fundamental building block for crafting bioactive peptides. Its integration into peptide sequences unlocks insights into protein-protein interactions and receptor binding dynamics. The compound's naphthyl moiety introduces hydrophobic nuances, facilitating the design of peptides with heightened stability and bioactivity.

Neuroscience Research: Delving into the intricate realms of neural pathways and neurotransmitter functions, scientists turn to γ-(2-Naphthyl)-D-β-homoalanine hydrochloride as a probing tool. Incorporating it into synthetic peptide analogs allows for in-depth exploration of neuropeptide activities and receptor responses, illuminating pathways relevant to neurological conditions and the formulation of cutting-edge neuropharmaceuticals.

Enzyme Inhibition Studies: In the realm of enzyme inhibition research, γ-(2-Naphthyl)-D-β-homoalanine hydrochloride takes center stage in assessing its impact on specific enzymatic activities. By engaging with enzyme active sites, researchers dissect inhibitory mechanisms and discern potential therapeutic avenues. This in-depth analysis aids in pinpointing novel targets for drug development and unraveling the intricacies of enzyme functionality, paving the way for groundbreaking advancements in biopharmaceutical sciences.

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