L-Aspartic acid α-4-nitroanilide hydrochloride
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L-Aspartic acid α-4-nitroanilide hydrochloride

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Category
L-Amino Acids
Catalog number
BAT-003921
CAS number
154564-03-1
Molecular Formula
C10H11N3O5·HCl
Molecular Weight
289.72
L-Aspartic acid α-4-nitroanilide hydrochloride
IUPAC Name
(3S)-3-amino-4-(4-nitroanilino)-4-oxobutanoic acid;hydrochloride
Synonyms
L-Asp-pNA HCl; N-(4-Nitrophenyl)-L-alpha-Asparagine Hydrochloride; (S)-3-Amino-4-((4-nitrophenyl)amino)-4-oxobutanoic acid hydrochloride
Appearance
Light yellow crystalline powder
Purity
≥ 99% (HPLC)
Melting Point
178-182 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C10H11N3O5.ClH/c11-8(5-9(14)15)10(16)12-6-1-3-7(4-2-6)13(17)18;/h1-4,8H,5,11H2,(H,12,16)(H,14,15);1H/t8-;/m0./s1
InChI Key
VVZGJGYVGBGMRI-QRPNPIFTSA-N
Canonical SMILES
C1=CC(=CC=C1NC(=O)C(CC(=O)O)N)[N+](=O)[O-].Cl

L-Aspartic acid α-4-nitroanilide hydrochloride is a biochemical reagent commonly used in various scientific applications. Here are some key applications of L-Aspartic acid α-4-nitroanilide hydrochloride:

Enzyme Activity Assays: This compound is frequently used as a substrate in enzyme activity assays, particularly for aspartic proteases. By measuring the rate of substrate cleavage, researchers can determine the activity levels of specific enzymes. This information is crucial for understanding enzyme kinetics and developing enzyme inhibitors.

Protein Engineering: In protein engineering research, L-Aspartic acid α-4-nitroanilide hydrochloride helps in testing the functionality of engineered proteins. It serves as a model substrate to evaluate how modifications in enzyme structure affect catalytic activity. This assists researchers in designing proteins with enhanced or altered functions for various biotechnological applications.

Diagnostic Development: L-Aspartic acid α-4-nitroanilide hydrochloride is utilized in the development of diagnostic assays for detecting enzyme-related diseases. By incorporating this substrate into diagnostic kits, clinicians can monitor the activity of specific enzymes in patient samples. This aids in the diagnosis and progression tracking of conditions such as liver diseases and certain cancers.

Biochemical Research: This compound is widely used in biochemical studies to explore the mechanisms of enzyme-substrate interactions. Researchers employ it to investigate binding affinities, reaction rates, and intermediate states of enzymatic processes. These studies contribute to a deeper understanding of enzyme function and regulation at the molecular level.

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