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Catalog Number:
04549
CAS Number:
5800-34-0
Glutaryl-L-phenylalanine 4-nitroanilide
Purity:
≥ 98% (HPLC)
Synonym(s):
Glutaryl-L-Phe-pNA
Temperature Sensitive
Documents
$45.00 /100MG
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Product Information

Glutaryl-L-phenylalanine 4-nitroanilide is a versatile compound with significant applications in biochemical research and pharmaceutical development. This compound serves as a valuable substrate in enzyme assays, particularly in studies involving proteases and peptidases, where it can help elucidate enzyme kinetics and mechanisms. Its unique structure, featuring a nitroaniline moiety, enhances its reactivity and specificity, making it an ideal candidate for developing sensitive detection methods in analytical chemistry.

Moreover, Glutaryl-L-phenylalanine 4-nitroanilide has shown potential in drug design and synthesis, particularly in the development of peptide-based therapeutics. Researchers can leverage its properties to create novel compounds with improved efficacy and selectivity. The compound's ability to mimic natural substrates allows for the exploration of new therapeutic pathways, making it a crucial tool for professionals in medicinal chemistry and biochemistry.

Synonyms
Glutaryl-L-Phe-pNA
CAS Number
5800-34-0
Purity
≥ 98% (HPLC)
Molecular Formula
C20H21N3O6
Molecular Weight
399.4
MDL Number
MFCD00038362
PubChem ID
3623356
Appearance
White powder/solid
Optical Rotation
[a]25D = 54 - 63 ° (C=1 in MeOH) (Lit.)
Conditions
Store at ≤ -20 °C
General Information
Synonyms
Glutaryl-L-Phe-pNA
CAS Number
5800-34-0
Purity
≥ 98% (HPLC)
Molecular Formula
C20H21N3O6
Molecular Weight
399.4
MDL Number
MFCD00038362
PubChem ID
3623356
Appearance
White powder/solid
Optical Rotation
[a]25D = 54 - 63 ° (C=1 in MeOH) (Lit.)
Conditions
Store at ≤ -20 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Glutaryl-L-phenylalanine 4-nitroanilide is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for proteases. Its ability to mimic natural substrates allows researchers to study enzyme kinetics and inhibition effectively.
  • Drug Development: In pharmaceutical research, it is used to evaluate the efficacy of new drugs targeting specific enzymes, helping to streamline the drug discovery process.
  • Diagnostic Tools: The compound can be incorporated into diagnostic kits for detecting enzyme-related disorders, providing a reliable method for early diagnosis.
  • Research on Protein Interactions: It aids in studying protein-ligand interactions, which is crucial for understanding cellular mechanisms and developing targeted therapies.
  • Educational Purposes: This compound is often utilized in academic laboratories to teach students about enzyme activity and biochemical techniques, enhancing practical learning experiences.

Citations