DL-Alanine β-naphthylamide hydrochloride
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DL-Alanine β-naphthylamide hydrochloride

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Category
DL-Amino Acids
Catalog number
BAT-003614
CAS number
74144-49-3
Molecular Formula
C13H14N2O·HCl
Molecular Weight
250.77
DL-Alanine β-naphthylamide hydrochloride
IUPAC Name
2-amino-N-naphthalen-2-ylpropanamide;hydrochloride
Synonyms
DL-Ala-βNA HCl; 2-amino-N-(naphthalen-2-yl)propanamide hydrochloride
Melting Point
258-260 °C
Storage
Store at 2-8°C
InChI
InChI=1S/C13H14N2O.ClH/c1-9(14)13(16)15-12-7-6-10-4-2-3-5-11(10)8-12;/h2-9H,14H2,1H3,(H,15,16);1H
InChI Key
WNLRRMRLNYQNOZ-UHFFFAOYSA-N
Canonical SMILES
CC(C(=O)NC1=CC2=CC=CC=C2C=C1)N.Cl

DL-Alanine β-naphthylamide hydrochloride, a chemical compound with diverse applications in biochemical and medical research, serves as a versatile tool in various scientific endeavors. Here are the key applications highlighted with high perplexity and burstiness:

Enzyme Activity Assays: Widely employed in enzyme activity assays, DL-Alanine β-naphthylamide hydrochloride emerges as a pivotal substrate, particularly for assessing the activity of peptidases and aminopeptidases. Upon hydrolysis by these enzymes, it releases β-naphthylamine, allowing for quantitative measurement. This enables researchers to delve into enzyme kinetics while facilitating the screening for enzyme inhibitors or activators through meticulous experimentation and analysis.

Microbial Identification: In the realm of microbiology, DL-Alanine β-naphthylamide hydrochloride assumes a crucial role in culture media as a diagnostic aide for identifying specific bacterial species. Specific bacteria possess the enzyme capable of hydrolyzing this substrate, triggering a discernible color change that serves as a telltale sign of their presence. This method stands as an invaluable tool in clinical laboratories, aiding in the swift and precise identification of pathogenic bacteria through intricate biochemical analyses and microbial interactions.

Cell Culture Studies: Within the domain of cell culture studies, DL-Alanine β-naphthylamide hydrochloride emerges as a pivotal component in investigating the metabolic activity and viability of cells. Acting as a fluorescent substrate, it facilitates the monitoring of cellular enzyme activity, offering insights into cell health under diverse experimental conditions. This application proves pivotal in drug screening initiatives and cytotoxicity testing efforts, shedding light on cellular responses and potential therapeutic interventions through meticulous experimentation and cellular observation.

Biochemical Pathway Analysis: Researchers leverage DL-Alanine β-naphthylamide hydrochloride to explore specific biochemical pathways associated with amino acid metabolism. By tracking the hydrolysis and subsequent reactions of this substrate, scientists can uncover the roles of various enzymes and intermediates, gaining profound insights into metabolic regulations and potential therapeutic targets. This rigorous analysis allows for a deeper understanding of intricate biochemical processes and metabolic interactions, driving forward research endeavors in addressing complex scientific inquiries.

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